Eto Yoshikatsu 衞藤義勝

… Alternative Names

衞藤義勝エトウヨシカツ

ETO Yoshikatsu 衞藤義勝

ETO Y. 衛藤義勝

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Researcher Number	50056909
External Links
Affiliation (Current)	2024: 一般財団法人脳神経疾患研究所, 先端医療研究センター, センター長
Affiliation (based on the past Project Information) *help	2021 – 2022: 一般財団法人脳神経疾患研究所, 先端医療研究センター, センター長 2014 – 2019: 一般財団法人脳神経疾患研究所, 先端医療研究センター, センター長 2014 – 2015: 東京慈恵会医科大学, 医学部, 名誉教授 2007 – 2013: Jikei University School of Medicine, 医学部, 教授 1998 – 2004: 東京慈恵会医科大学, 医学部, 教授 … More 1997 – 1999: Jikei University School of Medicine prof., 医学部・小児科, 教授 1996: The Jikei University School of Medicine prof., 小児科, 助手 1996: The Jikei University School of Medicine Prof., 小児科, 教授 1995: 東京慈恵会医科大学, 医学部・小児科学, 教授 1995: 東京慈恵会医科大学, 医学部・微生物学第一, 教授 1995: 東京慈恵会医科大学, 小児科学, 教授 1994: Jikei Univ.Dep.of Pediatr., prof., 医学部, 教授 1993: 東京慈恵会医科大学, 医学部・小児科, 助教授 1993: assistant professor, 小児科, 助教授 1990 – 1993: 東京慈恵会医科大学, 医学部, 助教授 1990: 東京慈恵会医科大学, 小児科学, 助教授 1988 – 1990: 東京慈恵会医科大学, 小児科, 助教授 1989: 東京慈恵会医科大学, 医学部小児科, 助教授 1988: THE JIKEI UNIVERSITY SCHOOL OF MEDICINE, DEPARTMENT OF PEDIATRICS 1986 – 1987: 東京慈恵会医科大学, 医学部, 助教授 1986: 慈恵医大, 医学部, 助教授 Less
Review Section/Research Field	Principal Investigator Pediatrics / Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Pediatrics / Pediatrics / Digestive surgery
Keywords	Principal Investigator 遺伝子治療 / ライソゾーム病 / ゴーシェ病 / iPS細胞 / MLD / 酵素補充療法 / ファブリー病 / アデノウイルスベクター / サイコシン / Krabbe病 … More / Twitcherマウス / 動物モデル / Gaucher disease / Gaucher病 / 神経細胞 / lysosomal disease / MS/MS / iPS cells / ポンぺ病 / 免疫寛容 / 異染性脳白質変性症 / RNAリプログラミング / 血管内皮細胞 / グロボトリアオシルセラミド (Gb3) / NPC病 / プロテオミクス / iPS細胞作製 / ニーマンピック病 / TEM解析 / oxysterol / lysoGb3 / 蓄積脂質 / Niemann-Pick C病 / タンデムMS / オキシステロール、 / バイオマーカー / ファブリ病 / NPC / Gaucher's disease / psychosine / Krabbe's disease / リポゾーム / 神経細胞培養 / アリルサルファターゼ / 脳変性疾患 / DNA診断 / Retrovirus vector / Krabbe disease / Pre-natal Gene therapy / Leucodystrophy / Gene Therapy / ムコ多糖症 / 遺伝性白質変性症 / レトロウイルスベクター / クラッベ病 / 出生前治療 / 遺伝性脳白質変性症 / Fabry disease / genetic disorder / chromosomal disorders / lectin method / prenatal diagnosis / fetal blood / maternal blood / CD71 / 胎児血 / 母体 / 遺伝病 / 染色体異常症 / レクチン法 / 出生前診断 / 胎児血球 / 母体血 / Sly mice / Twitcher mice / neural stem cell therapy / gene therapy / Sjogren-Larsson / 遺伝子異常 / Slyマウス / 神経幹細胞 / neuronal cells / Gene therapy / Gene analysis / lipidosis / 中枢神経症状 / 先天代謝異常症 / 造血幹細胞 / 遺伝子変異 / 遺伝子解析 / Conduritol-B-epoxedo (CBE) / glucocerebroside / 細胞内カルシウム濃度 / Conduritol-B-epoxide(CBE) / Human Oligodendroglioma(HOG)細胞 / glucosylsphingosine / プロティンキナーゼC活性 / スフィンゴリピド / glicosylsphingosine / ゴ-シェ病 / 遺伝性ロイコヂストロフィー症 / Metachromatic leukodystrophy(MLD) / グルコセレブロシダーゼ / Glucocerebrosidase / mannnose terminal / neuronal cell / blood brain barrier / liposome / αーマンノ-ス含有リポゾ-ム / 培養神経細胞 / α_2ーマクログロブリン / 脳障害 / リポゾ-ム / マンノ-ス / cerebrosideβ-galactosidase / グリア細胞 / リボゾ-ム / 酵素抗体染色 / ^ース / cerebrosideーβーgalactoside / 酵素補充法 / 脳血液関門 / 電子顕微鏡 / Nestin / GM2-ganglioside / 細胞治療 / Miglustat / Tay-Sacks病 / Pompe disease / Niemann-Pick disease / Fabry sisease / Tay-Sacks disease / Fabry 病 / Niemann-Pick病 / Tay-Sacks 病 / IPS 細胞 / 制御性T細胞 / 免疫応答 / アナフィラキシー / ポンペ病 / 抗CD3抗体 / 抗体 / ライソゾーム蓄積症 / 酵素補充湯療法 / RSV / CMVpromotor / SV-40 / ヘルペスウイルスベクター / ニーマンピック病マウス / クラッベ病マウス / リピドーシス / サルファターゼ / オリゴデンドロサイト / レトロウイルス / アデノウイルス / オリゴデンドログリア細胞 / GLD培養細胞 / ガラクトサミン / スフィンゴシングルコサイコシン / 中枢神経培養細胞 / ガラクトシ-ルーβーガラクトシダ-ゼ … More Except Principal Investigator 遺伝子治療 / Gaucher disease / beta-glucuronidase / gene therapy / レトロウイルスベクター / 遺伝子変異 / 酵素補充療法 / 遺伝子解析 / Sly disease / Sly病 / ゴ-シェ病 / 臨床表現型 / アデノウイルスベクター / ゴーシェ病 / 異染性脳白質変性症 / Gaucher病 / MLD / 動物モデル / mapping / SOX3 / Trf1 / LHX3 / HESX1 / PROP1 / PIT1 / adenovirus vector / fibrin glue / Twitcherマウス / MPS VII / Adenovirus / Gene Tharapy / 中枢神経 / リソゾーム病 / retrovirus / ムコ多糖症 / モデルマウス / ムコ多糖症VII型 / アデノウイルス / レトロウイルス / β-glucuronidase / Neurolipidosis / 骨髄移植 / Krabbe's disease / クラベ病 / ニーマンピック病 / Psychosine / コレステロ-ル / サイコシン / 遺伝子導入 / Lysosomal disorder / Niemann-Pick mouse / Twitcher mouse / (5)Twitcherマウス / (4)培養オリゴデンドロサイト / (3)脱髄 / (2)サイコシン / (1)krabbe病 / E-64 / 神経培養 / ライソゾ-ム病 / ニ-マンピック病 / Monoclonal antibody / Arylsulfatese A / 細胞内プロセシング / DNA診断 / アリルサルファターゼA.B,C-DNAのクローニング / C-DNAのクローニング / アミノ酸配列 / 精製 / アリルサルファターゼA・B / 抗体作成 / 酵素精製 / CDNAクローニング / モノクローナル抗体 / アリルサルファターゼA / Familial Congenital Panhypopituitarism / BRN2 / PTX2 / 先天性汎下垂体機能低下症 / 遺伝性先天性汎下垂体機能低下症 / 肝細胞 / 癌抑制遺伝子 / 転移性肝癌遺残 / lysosomal disorder / mutation / Twitcher マウス / ミクログリア / Cytkine / Adenovirus Vector / Niemann-Pick Disease TypeC / Neural progenitor / Nieman-Pick病typeC / Niemann-Pick病type C / サイトカイン / β-galactosidase / Nieman-Pick病type C / AAV / Gene Therapy / MPSVII / アデノ随伴ウイルス / phenotype / enzyme replacement therapy / 遺伝子異変 / metachromatic leukodystrophy / MPS VII mice / リソゾーム蓄積症 / 臨床症状 / Macrophage / Sly病(Sly disease) / Slyマウス / マクロファージ / Animal model / Gene mutation / Retrovirus / Inborn errors of metabolism / 遺伝子導入効率 / 中枢神経症状 / 先天代謝異常症 / transduction / CD34+ cells / adenovirus / 骨髄前駆細胞 / サザンブロット法 / CD34+細胞 / β-glucuronidase遺伝子 / ヒト骨髄細胞 / LTCIC(Long Term Culture Iniciating Cell) / NOD-SCIDマウス / 骨髄幹細胞(CD34+細胞) / 骨髄細胞 / L444P / common mutation / transplantation / Genotype / Phenotype / 胎児造血幹細胞 / 遺伝子変異分布 / SSCP法 / 神経型ゴ-シェ病 / 脳血液関門破壊 / 脳変性疾患 / PCR-SSCP / Arylsulfatase A / RT-PCR / Gaucher Disease / 遺伝型と臨床型 / アリルスルファターゼA遺伝子 / SSCP / ASO / PCR / PMD / PCR-SSCP法 / ArylsulfataseA / 遺伝子変異解析 / RT-PCR法 / matachromatic leukodystrophy(MLD) / 先天性ミエリン形成異常症 / retroviral vector / deficient cholesterol esterification / fetus gene therapy / Niemann-Pick disease type C / コレステロールエステル / Ca代謝 / 脳血液関門 / アデノウィルスベクター / 胎児肝臓 / Lacz遺伝子 / レトロウィルスベクター / コレステロールのエステル化障害 / 胎児遺伝子治療 / ヒトニーマンピック病タイプC / demyelination / genotype / Metachromatic / スプライスアクセプターサイト / PCR法 / 制限酵素 / ミエリン形成異常症 / 呼吸鎖リン酸化反応 / 脱髄 / 異染性白質変性症 / Nerve Growth Factor / Allergic gastroenteropathy / Macromolecules / free amino acid / Small intestine / Mucosal barrier / 免疫染色 / 小児アレルギ-性胃腸症 / viability / ラット小腸上皮細胞 / 空腸細胞 / 高分子蛋白の発育変動 / 遊離アミノ酸濃度 / 蛋白代謝 / 小腸細胞 / アレルギー性胃腸症 / 高分子蛋白 / 遊離アミノ酸 / 小腸 / 粘膜防御機構 / CDS mouse / SPM mouse / Cross hybridization / Genetic homogenity / Cholesterol esterification / Niemann-Pick Disease / 胎児肝細胞移植 / 細胞内転送機構 / コレステロ-ルエステル / NemannーPick病 / スフィンゴシェリン / 遺伝学的類似性 / エステル化障害 / CSDマウス / SPMマウス / スフィンゴミエリン / multiple sulfatase deficiency / ライソゾ-ム酵素 / リン酸化障害 / アルチプルサルファタ-ゼ欠損症 / アリルサルファタ-ゼA / マルチプルサルファタ-ゼ欠損症 / NGF receptor / Signal Transduction / Nimann-Pick Disease / Krabbe Disease / レトロウイルスベクタ- / Niemann-Pichマウス / リポゾ-ム療法 / マンノ-ス含有オリゴ糖 / Blood Brain barrier / スフィンゴミエリナ-ゼ / twitcherマウス / NiemannーPick病マウス / NGFRカスケ-ド / NGF / NGFRcDNA / golgiーlysosomal complex / NiemannーPickマウス / オリゴデンドログリア細胞 / Krabbe病 / 免疫寛容療法 / ポンペ病 / 経口投与 / 抗CD3抗体 / ライソゾーム病 / 免疫寛容 / 抗体 / ポンぺ病 / ファブリー病 / ライソゾーム病蓄積症 / 遺伝子発現 / 細胞小器官異常 / レセプター異常 / モデル動物 / 先天代謝異常 Less

Pathological analysis and drug screening using iPS cells derived from Fabry disease patientsPrincipal Investigator
- Principal Investigator
  
  衞藤義勝
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Southen Tohoku Research Institute for Neuroscience
Pathogenesis, Diagnosis and treatment of lysosomal diseases by Biomarker AnalysisPrincipal Investigator
- Principal Investigator
  
  Eto Yoshikatsu
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Southen Tohoku Research Institute for Neuroscience
Pathogenetic Stidies and Novel Enzyme Treatment using Fabry, Pompe and Tay-Sacks iPS cellsPrincipal Investigator
- Principal Investigator
  
  Eto Yoshikatsu
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Southen Tohoku Research Institute for Neuroscience
Development of effective treatment by immune tolerance induction in enzyme replacement therapy for lysosomal storage diseases
- Principal Investigator
  
  OHASHI TOYA
- Project Period (FY)
  2012 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei University School of Medicine
Anti-CD3 antibody induced immune tolerance to infused enzyme in enzyme replacement therapy for lysosomal storage diseasePrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei University School of Medicine
Immune tolerance induction in enzyme replacement therapy for lysosomal storage diseasesPrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei University School of Medicine
Elucidation of the mechanism of the development and differentiation of the human pituitary gland-Molecular analysis of candidate genes for familial congenital panhypopituitarism-
- Principal Investigator
  
  MIYATA Ichiro
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei University School of Medicine
Development of novel therapy and elucidation of pathophysiology for genetic leukodystrophyPrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei University School of Medicine
Loco-regional gene transfer by using fibrin glue system
- Principal Investigator
  
  TAKEYUKI Misawa
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Digestive surgery
- Research Institution
  JIKEI UNIVERSITY SCHOOL OF MEDICINE
Molecular Pathogenesis of Brain Damage and Gene Therapy in Genetic LeukodystrophyPrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  1999 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University Shool of Medicine
Prenatal Diagnosis of Ingenited Metabolic Disorders Using Maternal BloodPrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  1999 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University Shool of Medicine
Gene therapy for central nervous involvement of Gaucher disease
- Principal Investigator
  
  IDA Hiroyuki
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Gene Therapy for Sly disease using AAV vector.
- Principal Investigator
  
  OHASHI Touya
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Treatment for congenital metabolic disorder with brain dysfunction.
- Principal Investigator
  
  TOKORO Toshiharu
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Gene therapy for Krabbe disease with microglial cells derived from brain
- Principal Investigator
  
  GOMIBUCHI Ichizou
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Studies for Gene Therapy of SphingolipidosisPrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  1998 – 1999
- Research Category
  
  Grant-in-Aid for Scientific Research (B).
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Gene therapy for CNS involvement of Lysosomal storage disease using various viral vector
- Principal Investigator
  
  ITO Fumiyuki
- Project Period (FY)
  1998 – 1999
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Studies of inherited neurodegenerative disease ; mutation analysis and gene therapy
- Principal Investigator
  
  MAEKAWA K.
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Gene therapy for Sly disease
- Principal Investigator
  
  OHASHI T.
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Gene therapy for neuronopathic Gaucher disease
- Principal Investigator
  
  IDA H.
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
The cause of neuropathochemistry of inherited NeurodegenerationPrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  1996 – 1997
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
リピドーシス動物モデルを用いての中枢神経障害の遺伝子治療Principal Investigator
- Principal Investigator
  
  衛藤義勝
- Project Period (FY)
  1995
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei University School of Medicine
Gene Therapy toward to nuerodegenerative disorders using fetal hematopoietic stem cells transplantation
- Principal Investigator
  
  IDA Hiroyuki
- Project Period (FY)
  1995 – 1996
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Gene Therapy for Lysosomal Strage Disease
- Principal Investigator
  
  OHASHI Touya
- Project Period (FY)
  1995 – 1996
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
リピドーシス動物モデルを用いての中枢神経障害の遺伝子治療Principal Investigator
- Principal Investigator
  
  衛藤義勝
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei University School of Medicine
Molecular Analysis and Gene Therapy in Inherited dysmyelinating disorder
- Principal Investigator
  
  MAEKAWA Kihei
- Project Period (FY)
  1994 – 1996
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Gene therapy for inherited neurodegenerative disease using fetal bone marrows stem cell transplantation.
- Principal Investigator
  
  TOKORO Toshiharu
- Project Period (FY)
  1993 – 1994
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei Univ.School of Medicine
単一遺伝子病の分子・細胞生物学的研究、疾患発症の分子機構の解明
- Principal Investigator
  
  松田一郎
- Project Period (FY)
  1992 – 1993
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Research Institution
  Kumamoto University
Studies of genetic analysis and gene therapy for myelin-associated disorders.
- Principal Investigator
  
  MAEKAWA Kihei
- Project Period (FY)
  1992 – 1993
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
Genetic analysis of Niemann-Pick model mouse.
- Principal Investigator
  
  TOKORO Toshoharu
- Project Period (FY)
  1991 – 1992
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei Univ.School of Medicine
Developmental investigations of gut mucosal barrier in term of cell structure and immune response.
- Principal Investigator
  
  TOYODA Shigeru
- Project Period (FY)
  1991 – 1993
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine
リピド-シスマウス神経細胞に於けるガングリオシド代謝とその機能異常の解明Principal Investigator
- Principal Investigator
  
  衛藤義勝
- Project Period (FY)
  1990
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Research Institution
  Jikei University School of Medicine
Cellular engineering for treatment of animal model for inherited brain disorder
- Principal Investigator
  
  MAEKAWA K.
- Project Period (FY)
  1989 – 1991
- Research Category
  
  Grant-in-Aid for General Scientific Research (A)
- Research Field
  
  Pediatrics
- Research Institution
  Tokyo Jikei University School of Medicine
Pathogenesis of Multiple Sulfatase Deficiency
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  1989 – 1990
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Tokyo Jikei University School of Medicine
Modified enzyme which target to neuronal cells to cross blood brain barrierPrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  1989 – 1990
- Research Category
  
  Grant-in-Aid for Developmental Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Tokyo Jikei University School of Medicine
The Pathogenesis of Demyelination in Krabbe's disease and it's therapy
- Principal Investigator
  
  TOKORO Toshiharu
- Project Period (FY)
  1988 – 1989
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  The Jikei University School of Medicine, Department of Pediatrics
Molecular and biochemical analysis of inherited degernerative brain disorderPrincipal Investigator
- Principal Investigator
  
  ETO Yoshikatsu
- Project Period (FY)
  1986 – 1987
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Department of Pediatrics, Tokyo Jikei University School of Medicine
c DNA cloning for human Arylsulfatase A
- Principal Investigator
  
  ITO Fumiyuki
- Project Period (FY)
  1986 – 1988
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jikei University School of Medicine

[Book] ライソゾーム病のすべて2019
- Author(s)
  衞藤　義勝
- Total Pages
  151
- Publisher
  医歯薬出版
- Data Source
  KAKENHI-PROJECT-17K10067
[Book] 特集　ライソゾーム病　最新情報と将来展望2019
- Author(s)
  衞藤　義勝
- Total Pages
  1384
- Publisher
  日本臨床社
- Data Source
  KAKENHI-PROJECT-17K10067
[Book] ゴーシェ病と最新治療（酵素補充療法，基質合成抑制療法）2016
- Author(s)
  衞藤義勝
- Publisher
  The Lipid Vol.27 No.1
- Data Source
  KAKENHI-PROJECT-26461536
[Book] ゴーシェ病と最新治療（酵素補充療法，基質合成抑制療法）2016
- Author(s)
  衞藤義勝他
- Total Pages
  5
- Publisher
  メディカルレビュー社
- Data Source
  KAKENHI-PROJECT-26461536
[Book] iPS細胞を用いた難病研究-臨床病態解明と創薬に向けた研究の最新知見2015
- Author(s)
  中畑　龍俊、衞藤義勝　他
- Total Pages
  220
- Publisher
  株式会社　メディカルドゥ
- Data Source
  KAKENHI-PROJECT-26461536
[Book] ファブリー病症例集　vol.2　早期診断・早期治療のために2015
- Author(s)
  衞藤義勝他
- Total Pages
  117
- Publisher
  株式会社メディカルトリビューン
- Data Source
  KAKENHI-PROJECT-26461536
[Book] 医学のあゆみ2014
- Author(s)
  衞藤義勝
- Total Pages
  2
- Publisher
  医歯薬出版株式会社
- Data Source
  KAKENHI-PROJECT-26461536
[Book] ゴーシェ病　診断・治療ハンドブック2014
- Author(s)
  衞藤義勝　他
- Total Pages
  29
- Publisher
  株式会社イーエヌメディックス
- Data Source
  KAKENHI-PROJECT-26461536
[Book] 別冊日本臨牀　新領域別症候群シリーズ2014
- Author(s)
  衞藤義勝、衞藤　薫
- Total Pages
  7
- Publisher
  日本臨牀社
- Data Source
  KAKENHI-PROJECT-26461536
[Book] ファブリー病症例集　早期診断・早期治療のために2014
- Author(s)
  衞藤義勝他
- Total Pages
  98
- Publisher
  株式会社メディカルトリビューン
- Data Source
  KAKENHI-PROJECT-26461536
[Book] ポンペ病　2nd　edition2014
- Author(s)
  埜中征哉、衞藤義勝　他
- Total Pages
  134
- Publisher
  株式会社協和企画
- Data Source
  KAKENHI-PROJECT-26461536
[Book] 遺伝子診療学(第2版)遺伝子診断の進歩とゲノム治療の展望2010
- Author(s)
  衞藤義勝
- Total Pages
  12
- Publisher
  日本臨牀
- Data Source
  KAKENHI-PROJECT-21591333
[Book] EBM神経疾患の治療2007
- Author(s)
  衛藤義勝
- Publisher
  2007-2008中外医学社
- Data Source
  KAKENHI-PROJECT-19591223
[Book] EBM神経疾患の治療2007-20082007
- Author(s)
  衛藤義勝
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-19591223
[Book] ファブリー病について,ファブリー病2004
- Author(s)
  衛藤義勝, 井田博幸
- Total Pages
  7
- Publisher
  ブレーン出版(株)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Water intoxication: A clue to the presence of classical Fabry disease2022
- Author(s)
  Miyabayashi Takuya、Sato Ryo、Okubo Yukimune、Endo Wakaba、Inui Takehiko、Togashi Noriko、Yanagisawa Hiroko、Eto Yoshikatsu、Haginoya Kazuhiro
- Journal Title
  
  Brain and Development
  
  Volume: 44 Issue: 8 Pages: 592-593
- DOI
  10.1016/j.braindev.2022.07.001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07785
[Journal Article] A survey on the patient journey in Fabry disease in Japan2022
- Author(s)
  Tsurumi Mina、Ozaki Asuka、Eto Yoshikatsu
- Journal Title
  
  Molecular Genetics and Metabolism Reports
  
  Volume: 33 Pages: 100909-100909
- DOI
  10.1016/j.ymgmr.2022.100909
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07785
[Journal Article] Generation and characterization of motor neuron progenitors and motor neurons using metachromatic leukodystrophy-induced pluripotent stem cells2022
- Author(s)
  Hossain Mohammad Arif、Hasegawa-Ogawa Minami、Manome Yoko、Igarashi Miki、Wu Chen、Suzuki Ken、Igarashi Junko、Iwamoto Takeo、Okano Hirotaka James、Eto Yoshikatsu
- Journal Title
  
  Molecular Genetics and Metabolism Reports
  
  Volume: 31 Pages: 100852-100852
- DOI
  10.1016/j.ymgmr.2022.100852
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07785
[Journal Article] Characterization of cellular phenotypes in neurons derived from induced pluripotent stem cells of male patients with Fabry disease2022
- Author(s)
  Miyajima Takashi、Saito Ryo、Yanagisawa Hiroko、Igarashi Miki、Wu Chen、Iwamoto Takeo、Eto Yoshikatsu
- Journal Title
  
  Journal of Inherited Metabolic Disease
  
  Volume: 46 Issue: 1 Pages: 143-152
- DOI
  10.1002/jimd.12567
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07785
[Journal Article] Prevalence of patients with lysosomal storage disorders and peroxisomal disorders: A nationwide survey in Japan2021
- Author(s)
  Koto Yuta、Sakai Norio、Lee Yoko、Kakee Naoko、Matsuda Junko、Tsuboi Kazuya、Shimozawa Nobuyuki、Okuyama Torayuki、Nakamura Kimitoshi、Narita Aya、Kobayashi Hiroshi、Uehara Ritei、Nakamura Yoshikazu、Kato Koji、Eto Yoshikatsu
- Journal Title
  
  Molecular Genetics and Metabolism
  
  Volume: 133 Issue: 3 Pages: 277-288
- DOI
  10.1016/j.ymgme.2021.05.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07785
[Journal Article] A Phase 2/3 Trial of Pabinafusp Alfa, IDS Fused with Anti-Human Transferrin Receptor Antibody, Targeting Neurodegeneration in MPS-II2021
- Author(s)
  Okuyama Torayuki、Eto Yoshikatsu、Sakai Norio、Nakamura Kimitoshi、Yamamoto Tatsuyoshi、Yamaoka Mariko、Ikeda Toshiaki、So Sairei、Tanizawa Kazunori、Sonoda Hiroyuki、Sato Yuji
- Journal Title
  
  Molecular Therapy
  
  Volume: 29 Issue: 2 Pages: 671-679
- DOI
  10.1016/j.ymthe.2020.09.039
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07785
[Journal Article] Characteristics of the Electrocardiogram in Japanese Fabry Patients Under Long-Term Enzyme Replacement Therapy2021
- Author(s)
  Morimoto Satoshi、Nojiri Ayumi、Fukuro Eiko、Anan Ikuko、Kawai Makoto、Sakurai Ken、Kobayashi Masahisa、Kobayashi Hiroshi、Ida Hiroyuki、Ohashi Toya、Shibata Takahiro、Yoshimura Michihiro、Eto Yoshikatsu、Hongo Kenichi
- Journal Title
  
  Frontiers in Cardiovascular Medicine
  
  Volume: 7
- DOI
  10.3389/fcvm.2020.614129
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07785
[Journal Article] A neuropathological cell model derived from Niemann?Pick disease type C patient-specific iPSCs shows disruption of the p62/SQSTM1?KEAP1?NRF2 Axis and impaired formation of neuronal networks2021
- Author(s)
  Saito Ryo、Miyajima Takashi、Iwamoto Takeo、Wu Chen、Suzuki Ken、Hossain Mohammad Arif、Munakata Miyo、Era Takumi、Eto Yoshikatsu
- Journal Title
  
  Molecular Genetics and Metabolism Reports
  
  Volume: 28 Pages: 100784-100784
- DOI
  10.1016/j.ymgmr.2021.100784
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07785
[Journal Article] Dysregulated DNA methylation of GLA gene was associated with dysfunction of autophagy.2019
- Author(s)
  Yanagisawa H, Hossain MA, Miyajima T, Nagao K, Miyashita T, Eto Y.
- Journal Title
  
  Molecular Genetics Metabolism
  
  Volume: S1096-7192(19) Pages: 30014-9
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] Diagnostic performance evaluation of sulfate-conjugated cholesterol metabolites as urinary biomarkers of Niemann-Pick disease type C2019
- Author(s)
  Maekawa M, Narita A, Jinnoh I, Iida T, Marquardt T, Mengel E, Eto Y, Clayton PT, Yamaguchi H, Mano N.
- Journal Title
  
  Clin Chim Acta
  
  Volume: 494 Pages: 58-63
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] Future clinical and biochemical predictions of Fabry disease in females by methylation studies of the GLA gene.2019
- Author(s)
  Hossain MA, Wu C, Yanagisawa H, Miyajima T, Akiyama K, Eto Y.
- Journal Title
  
  Mol. Genet. Metab. Rep.
  
  Volume: 2019
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] Phenotypic variability of Niemann-Pick disease type C including a case with clinically pure schizophrenia: a case report.2018
- Author(s)
  1.Kawazoe T, Yamamoto T, Narita A, Ohno K, Adachi K, Nanba E, Noguchi A, Takahashi T, Maekawa M, Eto Y, Ogawa M, Murata M, Takahashi Y. Phenotypic variability of Niemann-Pick disease type C including a case with clinically pure schizophrenia: a case report. BMC Neurol. 2018 Aug 17;18(1):117.
- Journal Title
  
  BMC Neurol.
  
  Volume: 2018 Aug 1718(1) Pages: 117-117
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] The beneficial effects of long-term enzyme replacement therapy on cardiac involvement in Japanese Fabry patients.2018
- Author(s)
  3.Hongo K, Ito K, Date T, Anan I, Inoue Y, Morimoto S, Ogawa K, Kawai M, Kobayashi H, Kobayashi M, Ida H, Ohashi T, Taniguchi I, Yoshimura M, Eto Y.
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 2018 Jun;124(2) Pages: 143-151
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] A Case of Adult-onset Pompe Disease with Cerebral Stroke and Left Ventricular Hypertrophy.2018
- Author(s)
  Hossain MA, Miyajima T, Akiyama K, Eto Y
- Journal Title
  
  J Stroke　Cerebrovasc
  
  Volume: Dis. 2018 Nov
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] P-Tau and Subunit c Mitochondrial ATP Synthase Accumulation in the Central Nervous System of a Woman with Hurler-Scheie Syndrome Treated with Enzyme Replacement Therapy for 12 Years.2018
- Author(s)
  4.Kobayashi H, Ariga M, Sato Y, Fujiwara M, Fukasawa N, Fukuda T, Takahashi H, Ikegami M, Kosuga M, Okuyama T, Eto Y, Ida H.
- Journal Title
  
  JIMD Rep.
  
  Volume: 2018;41 Pages: 101-107
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] Characteristics of PPT1 and TPP1 enzymes in neuronal ceroid lipofuscinosis (NCL) 1 and 2 by dried blood spots (DBS) and leukocytes and their application to newborn screening.2018
- Author(s)
  5.Itagaki R, Endo M, Yanagisawa H, Hossain MA, Akiyama K, Yaginuma K, Miyajima T, Wu C, Iwamoto T, Igarashi J, Kobayashi Y, Tohyama J, Iwama K, Matsumoto N, Shintaku H, Eto Y.
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 2018 May;124(1) Pages: 64-70
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] Characteristics of PPT1 and TPP1 enzymes in neuronal ceroid lipofuscinosis (NCL) 1 and 2 by dried blood spots (DBS) and leukocytes and their application to newborn screening.2018
- Author(s)
  Itagaki R, Endo M, Yanagisawa H, Hossain MA, Akiyama K, Yaginuma K, Miyajima T, Wu C, Iwamoto T, Igarashi J, Kobayashi Y, Tohyama J, Iwama K, Matsumoto N, Shintaku H, Eto Y.
- Journal Title
  
  Mol Genet Metab.
  
  Volume: S1096-7192(18) Issue: 1 Pages: 30154-9
- DOI
  10.1016/j.ymgme.2018.03.007
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10067, KAKENHI-PROJECT-17H01539
[Journal Article] Application of a diagnostic methodology by quantification of 26:0　lysophosphatidylcholine in dried blood spots for Japanese newborn screening of X-linked adrenoleukodystrophy.2017
- Author(s)
  Wu C, Iwamoto T, Igarashi J, Miyajima T, Hossain MA, Yanagisawa H, Akiyama K, Shintaku H, Eto Y.
- Journal Title
  
  Mol Genet Metab Rep.
  
  Volume: １１ Pages: 115-118
- DOI
  10.1016/j.ymgmr.2017.06.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome.2017
- Author(s)
  Hossain MA, Yanagisawa H, Miyajima T, Wu C, Takamura A, Akiyama K, Itagaki R, Eto K, Iwamoto T, Yokoi T, Kurosawa K, Numabe H, Eto Y
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 120(3) Pages: 173-179
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Early onset of Fazio-Londe syndrome: the first case report from the Arabian Peninsula.2017
- Author(s)
  Hossain MA, Obaid A, Rifai M, Alem H, Hazwani T, Al Shehri A, Alfadhel M, Eto Y, Eyaid W.
- Journal Title
  
  Hum Genome
  
  Volume: 4 Issue: 1 Pages: 17018-17018
- DOI
  10.1038/hgv.2017.18
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] The severe clinical phenotype for a heterozygous Fabry female patient correlates to the methylation of non-mutated allele associated with chromosome 10q26 deletion syndrome.2017
- Author(s)
  Hossain MA, Yanagisawa H, Miyajima T, Wu C, Takamura A, Akiyama K, Itagaki R, Eto K, Iwamoto T, Yokoi T, Kurosawa K, Numabe H, Eto Y.
- Journal Title
  
  Molecular Genetics and Metabolism
  
  Volume: 120 Issue: 3 Pages: 173-179
- DOI
  10.1016/j.ymgme.2017.01.002
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26870831, KAKENHI-PROJECT-17K10067
[Journal Article] L-leucine and SPNS1 coordinately ameliorate dysfunction of autophagy in mouse and human Niemann-Pick type C disease.2017
- Author(s)
  Yanagisawa H, Ishii T, Endo K, Kawakami E, Nagao K, Miyashita T, Akiyama K, Watabe K, Komatsu M, Yamamoto D, Eto Y.
- Journal Title
  
  Sci Rep
  
  Volume: 7 Issue: 1 Pages: 15994-15994
- DOI
  10.1038/s41598-017-15305-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K06763, KAKENHI-PROJECT-17K10061, KAKENHI-PROJECT-17K10067, KAKENHI-PROJECT-17K19371, KAKENHI-PUBLICLY-17H05935, KAKENHI-PLANNED-25111006, KAKENHI-PROJECT-16H06371, KAKENHI-PROJECT-15K09729
[Journal Article] Ten-year-long enzyme replacement therapy shows a poor effect in alleviating giant leg ulcers in a male with Fabry disease.2017
- Author(s)
  Okada J, Hossain MA, Wu C, Miyajima T, Yanagisawa H, Akiyama K, Eto Y.
- Journal Title
  
  Mol Genet Metab Rep.
  
  Volume: 14 Pages: 68-72
- DOI
  10.1016/j.ymgmr.2017.12.004
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10067
[Journal Article] Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly: A case report.2016
- Author(s)
  Kuranobu N, Murakami J, Okamoto K, Nishimura R, Murayama K, Takamura A, Umeda T, Eto Y, Kanzaki S.
- Journal Title
  
  Hepatol Res.
  
  Volume: 46(5) Pages: 477-82
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST).2016
- Author(s)
  Saito O, Kusano E, Akimoto T, Asano Y, Kitagawa T, Suzuki K, Ishige N, Akiba T, Saito A, Ishimura E, Hattori M, Hishida A, Guili C, Maruyama H, Kobayashi M, Ohashi T, Matsuda I, Eto Y.
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 20(2): Pages: 284-93
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] A method for measuring disease-specific iduronic acid from the non-reducing end of glycosaminoglycan in mucopolysaccharidosis type II mice.2016
- Author(s)
  Shimada Y, Wakabayashi T, Akiyama K, Hoshina H, Higuchi T, Kobayashi H, ○Eto Y, Ida H, Ohashi T
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 117(2) Pages: 140-3
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly2016
- Author(s)
  Kuranobu N, Murakami J, Okamoto K, Nishimura R, Murayama K, Takamura A, Umeda T, ○Eto Y, Kanzaki S.
- Journal Title
  
  Hepatol Res.
  
  Volume: 46(5) Pages: 477-82
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] A method for measuring disease-specific iduronic acid from the non-reducing end of glycosaminoglycan in mucopolysaccharidosis type II mice. Mol Genet Metab.2016
- Author(s)
  Shimada Y, Wakabayashi T, Akiyama K, Hoshina H, Higuchi T, Kobayashi H, Eto Y, Ida H, Ohashi T.
- Journal Title
  
  Mol Genet Metab.2016 Feb;117(2):140-3.
  
  Volume: 117(2) Pages: 140-3
- Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST).2016
- Author(s)
  Saito O, Kusano E, Akimoto T, Asano Y, Kitagawa T, Suzuki K, Ishige N, Akiba T, Saito A, Ishimura E, Hattori M, Hishida A, Guili C, Maruyama H, Kobayashi M, Ohashi T, Matsuda I, ○Eto Y
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 20(2) Issue: 2 Pages: 284-93
- DOI
  10.1007/s10157-015-1146-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Identification of Cryptic Novel α-Galactosidase A Gene Mutations: Abnormal mRNA Splicing and Large Deletions.2016
- Author(s)
  Higuchi T, Kobayashi M, Ogata J, Kaneshiro E, Shimada Y, Kobayashi H, Eto Y, Maeda S, Ohtake A, Ida H, Ohashi T.
- Journal Title
  
  JIMD Rep.
  
  Volume: 2016 Jun 3.
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] A method for measuring disease-specific iduronic acid from the non-reducing end of glycosaminoglycan in mucopolysaccharidosis type II mice2016
- Author(s)
  Yohta Shimada, Taichi Wakabayashi, Kazumasa Akiyama, Hiroo Hoshina, Takashi Higuchi, Hiroshi Kobayashi, Yoshikatsu Eto, Hiroyuki Ida, Toya Ohashi
- Journal Title
  
  Molecular Genetics and Metabolism
  
  Volume: 117 Pages: 140-143
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Characteristics of Cerebral Microbleeds in Patients with Fabry Disease.2016
- Author(s)
  Kono Y, Wakabayashi T, Kobayashi M, Ohashi T, Eto Y, Ida H, Iguchi Y.
- Journal Title
  
  J Stroke Cerebrovasc Dis.
  
  Volume: 2016 Jun Pages: 1320-5
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly: A case report2015
- Author(s)
  Naomi Kuranobu,Jun Murakami,Ken Okamoto,Rei Nishimura,Kei Murayama,Ayumi Takamura,Toshiko Umeda,Yoshikatsu Eto and Susumu Kanzaki
- Journal Title
  
  Hepatology Research
  
  Volume: Aug 18 Issue: 5 Pages: 1-6
- DOI
  10.1111/hepr.12574
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Disease modeling and lentiviral gene transfer in patient-specific induced pluripotent stem cells from late-onset Pompe disease patient2015
- Author(s)
  Yohei Sato, Hiroshi Kobayashi, Takashi Higuchi, Yohta Shimada, Takumi Era, Shigemi Kimura, Yoshikatsu Eto, Hiroyuki Ida and Toya Ohashi
- Journal Title
  
  Molecular Therapy
  
  Volume: 15023 Pages: 1-8
- DOI
  10.1038/mtm.2015.23
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Identification of a novel GLA MUTATION (F69l) in a Japanese Patient with late onset Fabry disease.2015
- Author(s)
  Umeda T., Hashimoto S., Takamura A., Fujisaki M., Eto Y.
- Journal Title
  
  Human Genome Variation
  
  Volume: 15044 Issue: 1 Pages: 1-3
- DOI
  10.1038/hgv.2015.44
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Hematopoietic Stem Cell Gene Therapy Corrects Neuropathic Phenotype in Murine Model of Mucopolysaccharidosis Type II2015
- Author(s)
  Taichi Wakabayashi, Yohta Shimada, Kazumasa Akiyama, Takashi Higuchi, Takahiro Fukuda, Hiroshi Kobayashi, Yoshikatsu Eto, Hiroyuki Ida, and Toya Ohashi
- Journal Title
  
  HUMAN GENE THERAPY
  
  Volume: 26 Issue: 6 Pages: 357-366
- DOI
  10.1089/hum.2014.158
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Systemic accumulation of undigested lysosomal metabolites in an autopsy case of mucolipidosis type II; autophagic dysfunction in cardiomyocyte.2014
- Author(s)
  3.Sato Y, Kobayashi H, Sato S, Shimada Y, Fukuda T, Eto Y, Ohashi T, Ida H.
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 112 Pages: 224-28
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] A practical fluorometric assay method to measure lysosomal acid lipase activity in dried blood spots for the screening of cholesteryl ester storage disease and Wolman disease.2014
- Author(s)
  4.Dairaku T, Iwamoto T, Nishimura M, Endo M, Ohashi T, Eto Y.
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 111 Pages: 193-96
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] The generation of induced pluripotent stem cells (iPSCs) from patients with infantile and late-onset types of Pompe disease and the effects of treatment with acid-α-glucosidase in Pompe's iPSCs.2014
- Author(s)
  1.Higuchi T, Kawagoe S, Otsu M, Shimada Y, Kobayashi H, Hirayama R, Eto K, Ida H, Ohashi T, Nakauchi H, Eto Y.
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 112 Pages: 44-48
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Enzyme augmentation therapy enhances the therapeutic efficacy of bone marrow transplantation in mucopolysaccharidosis type II mice.2014
- Author(s)
  2.Akiyama K, Shimada Y, Higuchi T, Ohtsu M, Nakauchi H, Kobayashi H, Fukuda T, Ida H, Eto Y, Crawford BE, Brown JR, Ohashi T.
- Journal Title
  
  Mol Genet Metab.
  
  Volume: 111 Pages: 139-46
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461536
[Journal Article] Minimum requirement of donor cells to reduce the glycolipid storage following bone marrow transplantation in a murine model of Fabry disease2011
- Author(s)
  Yokoi T, Kobayashi H, Shimada Y, Eto Y, Ishige N, Kitagawa T, Otsu M, Nakauchi H, Ida H, Ohashi T
- Journal Title
  
  J Gene Med
  
  Volume: 13 Issue: 5 Pages: 262-8
- DOI
  10.1002/jgm.1566
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591333, KAKENHI-PROJECT-23659533
[Journal Article] Oral administration of recombinant human acid alpha -glucosidase reduces specific antibody formation against enzyme in mouse2011
- Author(s)
  Ohashi T, Iizuka S, Shimada Y, Eto Y, Ida H, Hachimura S, Kobayashi H
- Journal Title
  
  Mol Genet Metab
  
  Volume: 103 Pages: 98-100
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591333
[Journal Article] Pathology of the First Autopsy Case Diagnosed as Mucolipidosis type III alpha/beta Suggesting Autophagic Dysfunction2011
- Author(s)
  Kobayashi H, Eto Y, et al
- Journal Title
  
  Mol Genet Metab
  
  Volume: 102 Pages: 170-175
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591333
[Journal Article] Prognostic factors for the late onset Pompe disease with enzyme replacement therapy : from our experience of 4 cases including an autopsy case2010
- Author(s)
  Kobayahsi H, Eto, et al
- Journal Title
  
  Mol Genet Metab
  
  Volume: 100 Pages: 14-19
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591333
[Journal Article] Single gene disorder: recent advances of research.2010
- Author(s)
  Eto Y.
- Journal Title
  
  Nippon Rinsho
  
  Volume: 68 Pages: 117-128
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591333
[Journal Article] Japan Elaprase Treatment (JET) study : idursulfase enzyme replacement therapy in adult patients with attenuated Hunter syndrome (Mucopoly saccharidosis II, MPS II).2010
- Author(s)
  Okuyama T, Tanaka A, Suzuki Y, Ida H, Tanaka T, Cox GF, Eto Y
- Journal Title
  
  Mol Genet Metab
  
  Volume: 99 Pages: 18-25
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591333
[Journal Article] Neonatal gene transfer using lentiviral vector for murine Pompe disease : long term expression and glycogen reduction.2010
- Author(s)
  Kyosen OS, Iizuka S, Kobayashi H, Kimura T, Fukuda T, Shen JS, Shimada Y, Ida H, Eto Y
- Journal Title
  
  Gene Therapy
  
  Volume: 17 Pages: 521-530
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591333
[Journal Article] Induced pluripotent stem cells derived from mouse models of lysosomal storage disorders.2010
- Author(s)
  Xing-Li Meng, Jin-Song Shen, Shiho Kawagoe, Toya Ohashi, Roscoe O Brady, Yoshikatu Eto
- Journal Title
  
  PNAS
  
  Volume: 17 Pages: 7886-7891
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591333
[Journal Article] Reduced alfa-gal enzyme activity in Fabry fibroblast cells and Fabrymice tissues induced by serum from antibody positive patients with Fabry disease2008
- Author(s)
  Ohashi T, Iizuka S, Ida H, Eto Y.
- Journal Title
  
  Mol Genet Metab 94
  
  Pages: 313-31
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Reduced alpha-Gal A enzyme activity in Fabry fibroblast cellsand Fabry mice tissues induced by serum from antibody positivepatients with Fabry disease.2008
- Author(s)
  Ohashi T, Iizuka S, Ida H, Eto Y.
- Journal Title
  
  Mol Genet Metab. 94
  
  Pages: 313-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Non-invasive high-risk screening for Fabry disease hemizygotesand heterozygotes.2008
- Author(s)
  Kitagawa T, Suzuki K, Ishige N, Ohashi T, Kobayashi M, Eto Y, Tanaka A, Odaka H, Owada M.
- Journal Title
  
  Pediatr Nephrol. 23
  
  Pages: 461-71
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Lysosomal storage diseases : new challenges.2008
- Author(s)
  Scarpa M, Eto Y.
- Journal Title
  
  Acta Paediatr 97
  
  Pages: 5-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Clinical manifestations and natural history of Japanese heterozygous females with Fabry disease.2008
- Author(s)
  Kobayashi M, Ohashi T, Sakuma M, Ida H, Eto Y.
- Journal Title
  
  J Inherit Metab Dis. Jan 21(Online Report)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Immunogene therapy by adenovirus vector expressing CD40 ligandfor metastatic liver cancer in rats.2008
- Author(s)
  Hanyu K, Iida T, Shiba H, Ohashi T, Eto Y, Yanaga K.
- Journal Title
  
  Anticancer Res. 28
  
  Pages: 2785-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Reduced a-Gal A enzyme activity in Fabry fibroblast cells and Fabry mice tissues induced by serum from antibody positive patients with Fabry disease.2008
- Author(s)
  Ohashi T, Iizuka S, Ida H, Eto Y.
- Journal Title
  
  Mol. Gene. Metab. (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Cell Therapy for Peripheral Diseases and Reconstructive applications: Transplantation for lysosomal storage diesase. Halberstadt C, Emerich D ed. Cellular transplantation from laboratory to clinic . Cellular transplantation.2007
- Author(s)
  Ohashi T, Eto Y.
- Journal Title
  
  Amsterdam. Academic Press.
  
  Pages: 205-14
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] 蛋白尿、頭痛、四肢の激痛で来院した26歳男性2007
- Author(s)
  衛藤義勝
- Journal Title
  
  New専門医を目指すケース・メソッド・アプローチ5腎臓疾患
  
  Pages: 106-13
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Influence of antibody formation on reduction of globotriaosylceramide (GL-3) in urine from Fabry patients during agalsidase beta therapy2007
- Author(s)
  Ohashi T, Sakuma M, Kitagawa T, Suzuki K, Ishige N, Eto Y.
- Journal Title
  
  Mol Genet Metab 92
  
  Pages: 271-273
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] Influence of antibody formation on reduction of globotriaosylc eramide (GL-3) in urine from Fabry patients during agalsidase beta therapy.2007
- Author(s)
  Ohashi T, Sakuma M, Kitagawa T, Suzuki K, Ishige N, Eto Y.
- Journal Title
  
  Mol. Gene. Metab. 92
  
  Pages: 271-273
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] リソゾーム病.2007
- Author(s)
  衛藤義勝
- Journal Title
  
  月間臨床神経科学. 25
  
  Pages: 1280-2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591223
[Journal Article] GALC transduction leads to morphological improvement of the twitcher oligodendrocytes in vivo.2005
- Author(s)
  Meng XL, Shen JS, Watabe K, Ohashi T, Eto Y.
- Journal Title
  
  Mol Genet Metab. (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Widespread and highly persistent gene transfer to the CNS by retrovirus vector in utero : Implication for gene therapy to Krabbe disease.2005
- Author(s)
  Shen JS, Meng XL, Yokoo T, Sakurai K, Watabe K, Ohashi T, Eto Y.
- Journal Title
  
  J Gene Med. (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Widespread and highly persistent gene transfer to the CNS by retrovirus vector in utero : Implication for gene therapy to Krabbe disease.2005
- Author(s)
  Shen JS, Meng XL, Yokoo T, Sakurai K, Watabe K, Ohashi T, Eto Y.
- Journal Title
  
  J Gene Med (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] A novel mutation of the arginine vasopressin receptor 2 gene in a patient with congenital nephrogenic diabetes insipidus.2005
- Author(s)
  Tajima A, Miyata I, Katayama A, Toyoda S, Eto Y
- Journal Title
  
  Clinical Pediatric Endocrinology 14(1)
  
  Pages: 27-33
- NAID
  130004430945
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591136
[Journal Article] Functional analysis of the novel S179R Pit-1 mutant.2005
- Author(s)
  Miyata I, Yoshikawa H, Takeuchi M, Tojo K, Tajima N, Eto Y, Brue T
- Journal Title
  
  Proceedings of the 36th International Symposium on Growth Hormone and Growth Factors in Endocrinology and Metabolism 36
  
  Pages: 125-125
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591136
[Journal Article] Treatment of lysosomal storage disorders : Cell therapy and gene therapy.2004
- Author(s)
  Eto Y, Shen JS, Meng XL, Ohashi T
- Journal Title
  
  J Inherit Metab Dis 27(3)
  
  Pages: 411-415
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591136
[Journal Article] 先天性代謝異常症疾患モデル動物2004
- Author(s)
  衛藤義勝
- Journal Title
  
  別冊医学のあゆみ
  
  Pages: 73-75
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Treatment of lysosomal storage disorders : Cell therapy and gene therapy.2004
- Author(s)
  Eto Y, Shen JS, Meng XL, Ohashi T.
- Journal Title
  
  J Inherit Metab Dis. 27(3)
  
  Pages: 411-415
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Constitutionally tall stature with Morphological abnormality of the pituitary gland.2004
- Author(s)
  Miyata I, Yoshikawa H, Eto Y
- Journal Title
  
  Endocrine Journal 51(2)
  
  Pages: 189-195
- NAID
  80016601019
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591136
[Journal Article] Widespread gene transduction to the central nervous system by adenovirus in utero : Implication for prenatal gene therapy to brain involvement of lysosomal storage disease2004
- Author(s)
  Shen JS, Meng XL, Maeda H, Ohashi T, Eto Y.
- Journal Title
  
  J Gene Med 6(11)
  
  Pages: 1206-1215
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Widespread gene transduction to the central nervous system by adenovirus in utero : Implication for prenatal gene therapy to brain involvement of lysosomal storage disease.2004
- Author(s)
  Shen JS, Meng XL, Maeda H, Ohashi T, Eto Y.
- Journal Title
  
  J Gene Med. 6(11)
  
  Pages: 1206-1215
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Brain transplantation of genetically modified bone marrow stromal cells corrects CNS pathology and cognitive function in MPS VII mice.2004
- Author(s)
  Sakurai K, Iizuka S, Shen JS, Meng XL, Mori T, Umezawa A, Ohashi T, Eto Y
- Journal Title
  
  Gene Ther 11(19)
  
  Pages: 1475-1481
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Widespread gene transduction to the central nervous system by adenovirus in utero : Implication for prenatal gene therapy to brain involvement of lysosomal storage disease.2004
- Author(s)
  Shen JS, Meng XL, Maeda H, Ohashi T, Eto Y.
- Journal Title
  
  J Gene Med 6(11)
  
  Pages: 1206-1215
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Brain transplantation of genetically modified bone marrow stromal cells corrects CNS pathology and cognitive function in MPS VII mice.2004
- Author(s)
  Sakurai K, Iizuka S, Shen J-S, Meng X-L, Mori T, Umezawa A, Ohashi T, Eto Y
- Journal Title
  
  Gene Therapy 11
  
  Pages: 1475-1481
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591136
[Journal Article] Brain transplantation of genetically modified bone marrow stromal cells corrcts CNS pathology and cognitive function in MPS VII mice.2004
- Author(s)
  Sakurai K, Iizuka S, Shen JS, Meng XL, ori_T, _Umezawa A, Ohashi T, Eto Y
- Journal Title
  
  Gene Ther 11(19)
  
  Pages: 1475-1481
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Brain transplantation of genetically modified bone marrow stromal cells corrects CNS pathology and cognitive function in MPS VII mice.2004
- Author(s)
  Sakurai K, Iizuka S, Shen JS, Meng XL, Mori T, Umezawa A, Ohashi T, Eto Y.
- Journal Title
  
  Gene Ther. 11(19)
  
  Pages: 1475-1481
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Braintransplantation of genetically engineered human neural stem cells globally corrects brain lesions in the mucopolysaccharidosis type VII mouse.2003
- Author(s)
  Meng XL, Shen JS, Ohashi T, Maeda H, Kim SU, Eto Y.
- Journal Title
  
  J Neurosci Res. 74(2)
  
  Pages: 266-277
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14370252
[Journal Article] Novel treatment for neuropathic lysosomal storage diseases-cell therapy/gene therapy.2002
- Author(s)
  Eto Y, Ohashi T
- Journal Title
  
  Current Molecular Medicine 2(1)
  
  Pages: 83-89
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591136
[Journal Article] Administration of anti-CD3 antibodies modulates the immune response to an infusion of alpha-glucosidase in mice
- Author(s)
  Toya Ohashi, Sayoko Iizuka, Yohta Shimada, Takashi Higuchi, Yoshikatsu Eto, Hiroyuki Ida, Hiroshi Kobayashi
- Volume
  (投稿中)
- Data Source
  KAKENHI-PROJECT-21591333
[Journal Article] Functional and Structural Analysis of the Novel S179R Pit-1 Mutant.
- Author(s)
  Miyata I, Reynaud R, Vallette-Kasic S, Takeuchi M, Yoshikawa H, Tajima A, Tojo K, Gueydan M, Enjalbert A, Tajima N, Eto Y, Brue T
- Journal Title
  
  J Clin Endocrinol Metab (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591136
[Presentation] Comparative proteomics of Fabry and NPC diseases by skin fibroblasts and iPS cells derived neurons2022
- Author(s)
  Chen Wu, Takeo Iwamoto, Miki Igarashi, Takashi Miyajima, Ken Suzuki, Miyo Munakata, Yoshikatsu Eto
- Organizer
  The 63nd Annual Meeting of the Japanese Society for Inherited Metabolic Diseases
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] 東京都における拡大新生児スクリーニングの試験研究 (第2報)2022
- Author(s)
  石毛信之, 渡辺和宏, 長谷川智美, 小林正久, 加藤環, 齋藤加代子, 阿部祐一, 森岡一郎, 衞藤義勝, 石毛美夏, 大石公彦
- Organizer
  第63回日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] 10年間のFabry病ハイリスクスクリーニング1543例の解析2022
- Author(s)
  宮島任司, Chen Wu, 鈴木健, 五十嵐美樹, 宗形ミヨ, 岩本武夫, 衞藤義勝
- Organizer
  第63回日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] Prevalence of patients with lysosomal storage disorders and peroxisomal disorders in Japan2021
- Author(s)
  Yuta Koto, Norio Sakai, Yoko Lee, Torayuki Okuyama, Yoshikatsu Eto
- Organizer
  第62回日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] A survey on the Patient Journey of Fabry disease patients of Japan2021
- Author(s)
  Junko Yotsumoto, Mina Tsurumi, Asuka Ozaki, Yoshikatsu Eto
- Organizer
  第62回日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] ファブリー病患者由来iPS細胞から分化した神経細胞の病態解析に関する研究2021
- Author(s)
  宮島任司, 齋藤僚, 柳澤比呂子, Chen Wu, 五十嵐美樹, Mohammad Arif Hossain, 岩本武夫, 衞藤義勝
- Organizer
  第62回日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] Preliminary results of characterization on passages of cells from lysosomal diseases by proteomics2021
- Author(s)
  Chen Wu, Takeo Iwamoto, Takashi Miyajima, Miki Igarashi, Mohammad Arif Hossain, Junko Igarashi, Miyo Munakata, Ken Suzuki, Yoshikatsu Eto
- Organizer
  第62回日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] ファブリ病同一遺伝子家系に対するMigalastatの反応性並びに治療効果に関する研究2021
- Author(s)
  衞藤義勝, 宮島任司, ホセインモハンマドアリフ, ウーチェン, 鈴木健, 五十嵐美樹, 宗形ミヨ, 五十嵐純子, 岩本武夫
- Organizer
  第62回日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] Molecular pathogenesis of Neurons differentiated from iPS cells derived from NPC patients2021
- Author(s)
  Takashi Miyajima, Ryo Saito, Takeo Iwamoto, Chen Wu, Miki Igarashi, Mohammad Arif Hossain, Miyo Munakata, Ken Suzuki, Takumi Era, Yoshikatsu Eto
- Organizer
  第62回日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-21K07785
[Presentation] Development of neuropathological model using Niemann-Pick type C patient-derived iPSCs2020
- Author(s)
  Saito R., Miyajima T., Wu Chen, M. Arif Hossain, Itagaki R., Akiyama K., Iwamoto T., Eto Y
- Organizer
  The 140th Annual Meeting of the Pharmaceutical Society of Japan
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] DNA methylation study of GLA gene and its association with autophagy and clinical severity of heterozygous Fabry disease females.2020
- Author(s)
  M. Arif Hossain, Wu Chen, Yanagisawa H., Miyajima T., Saito R., Akiyama K., Eto Y.
- Organizer
  World sy,mposiu, 2020
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] Development of neuropathological model using Niemann-Pick type C patients derived iPSCs2020
- Author(s)
  Saito R., Miyajima T., Wu Chen, M. Arif Hossain, Itagaki R., Akiyama K., Iwamoto T., Eto Y.,
- Organizer
  World symposium, 2020
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] An update on biomarkers of 7-ketocholesterol, lyso-sphingomyelin, bile acid and glucosyl-sphingosine for Niemann-Pick disease type C2020
- Author(s)
  Wu Chen, Iwamoto T. M. Arif Hossain, Akiyama K. Igarashi J., Miyajima T., Saito R., Eto Y.,
- Organizer
  World symposium, 2020
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] Future clinical and biochemical predictions of Fabry disease in females by methylation studies of the GLA gene.; M. Arif Hossain2019
- Author(s)
  M. Arif Hossain, Wu Chen, Yanagisawa H., Miyajima T., Akiyama K., Saito R., Eto Y
- Organizer
  The 61st Annual Meeting of the Japanese Society for Inherited Metabolic Diseases
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 日本人 Fabry 病家系の遺伝子変異の研究：遺伝子変異－臨床病型相関と migalastat－amenable mutation 保有率2018
- Author(s)
  ○ 小林　正久 1, 金城　栄子 1, 大橋　十也 2, 衞藤　義勝 3, 井田　博幸 1 1 東京慈恵会医科大学　小児科, 2 東京慈恵会医科大学　総合医科学センター　遺伝子治療研究部 3 脳神経疾患研究所　先端医療研究センター
- Organizer
  第６０回　日本先天代謝異常学会、岐阜、１１月８～１０、２０１８
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] ニーマンピックC型の診断バイオマーカー：血清Lysosphongomyelin 測定の有用性に関する研究2017
- Author(s)
  衞藤義勝,　Chen Wu, 岩本武夫, 柳澤比呂子, 秋山けい子, 宮島任司, 五十嵐純子, Mohammad Arif Hossain
- Organizer
  第31回日本小児脂質研究会学術集会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] Special Lecture2.2017
- Author(s)
  Yoshikatsu Eto, Moderator
- Organizer
  第5回アジアLSDスクリーニング会議
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 神経変性疾患の遺伝子治療―今後の新しい治療展開2017
- Author(s)
  特別講演　司会　衞藤義勝
- Organizer
  第2回神経代謝病研究会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 乾燥濾紙血（DBS）による神経セロイドリポフスチン症（NCL）Ⅰ/Ⅱ型　新生児スクリーニングの研究2017
- Author(s)
  板垣里奈, 栁沼恵子, 遠藤昌弘, 秋山けい子, 柳澤比呂子, 岩本武夫, 新宅治夫, 衞藤義勝
- Organizer
  日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 「脂質代謝異常に潜む治療可能な稀少疾患：ライソゾーム酸性リパーゼ欠損症（LAL-D）」2017
- Author(s)
  教育セミナー　座長：衞藤義勝
- Organizer
  第31回日本小児脂質研究会学術集会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] Special Lecture, Lysosomal Storage Disorders: A model of Innovate Drug Development for the Rare Genetic Disorders.2017
- Author(s)
  Yoshikatsu Eto
- Organizer
  2017 Annual Conference of Medical Genetics& Genomics at AMC.
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] PL6-Plenary Session 6-Trends in organelle disease2017
- Author(s)
  Chair :Y Eto
- Organizer
  September 8, ICIEM 2017 13th International Congress of Inborn Errors of Metabolism. Rio de Janeiro, Brazil.
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] ポスター会場　知的障害を合併した重症型ファブリ病ヘテロ症例2017
- Author(s)
  フセイン・アリフ,衞藤　義勝他
- Organizer
  第120回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 乾燥濾紙血（DBS）を用いたムコ多糖症Ⅶ型（MPS Ⅶ）のハイリスクスクリーニングの検討2017
- Author(s)
  宮島任司, 五十嵐純子, Chen Wu, 柳澤比呂子, Mohammad Arif Hossain,秋山けい子, 濱﨑考史, 岩本武夫, 衞藤義勝
- Organizer
  日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 多変量解析で得た新規診断マーカー候補によるニーマンピック病C型の診断2017
- Author(s)
  Chen Wu, 岩本武夫, 柳澤比呂子, 秋山けい子, 宮島任司, 五十嵐純子, Mohammad Arif Hossain, 衞藤義勝
- Organizer
  日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 女性ヘテロ結合ファブリー病患者におけるオートファジーとメチル化との関連2017
- Author(s)
  柳澤比呂子, ホセイン・モハンマド・アリフ, 宮島任司, 秋山けい子, 衞藤義勝
- Organizer
  日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] CpG アイランドのメチル化によるFabry ヘテロ接合女性患者の臨床表現型予測について2017
- Author(s)
  Mohammad Arif Hossain, Chen Wu, 宮島任司, 柳澤比呂子, 秋山けい子, 岩本武夫, 衞藤義勝
- Organizer
  日本先天代謝異常学会　10月　川越
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 重度ヘテロ結合Fabry女性の予測診断に向けたメチル化に関する研究2017
- Author(s)
  Mohammad Arif Hossain, Chen Wu, 宮島任司, 柳澤比呂子, 秋山けい子, 岩本武夫, 衞藤義勝.
- Organizer
  日本人類遺伝学会　第62回大会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] ファブリー病患者の年齢、性別、及び酵素補充療法に起因する抗体価と血漿中LysoGb3の相関関係2017
- Author(s)
  Chen Wu, 岩本武夫, Mohammad Arif Hossain, 宮島任司, 秋山けい子, 柳澤比呂子, 五十嵐純子, 衞藤義勝
- Organizer
  日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] ニーマンピック病C型の診断：ハイリスクスクリーニングに関して2017
- Author(s)
  衞藤義勝
- Organizer
  第120回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] 乾燥濾紙血（DBS）を用いたムコ多糖症Ⅶ型（MPS Ⅶ）のハイリスクスクリーニングの検討2017
- Author(s)
  宮島任司, 五十嵐純子, Chen Wu, 柳澤比呂子, Mohammad Arif Hossain,　秋山けい子, 濱﨑考史, 岩本武夫, 衞藤義勝
- Organizer
  日本先天代謝異常学会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] Application of Lysosphingomyelin Measuremane for Diagonosis of Japanese patients with Niemann Pick Type C by MS/MS.2017
- Author(s)
  Chen Wu, 岩本武夫, 柳澤比呂子, 秋山けい子, 宮島任司, 五十嵐純子, Mohammad Arif Hossain, 衞藤義勝。
- Organizer
  第22回日本ライソゾーム病研究会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] Keynote presentation2017
- Author(s)
  Yoshikatsu Eto
- Organizer
  24-26 March 2017, Dublin, Ireland
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] An adult onset Pompe Disease with cerebral stroke and left ventricular hypertrophy.2017
- Author(s)
  Mohammad Arif Hossain, Takashi Miyajima, Keiko Akiyama, Hiroko Yanagisawa, Chen Wu, Takeo Iwamoto, Yoshikatsu Eto.
- Organizer
  第22回日本ライソゾーム病研究会
- Data Source
  KAKENHI-PROJECT-17K10067
[Presentation] ニーマンピック C 病：タンデムマスによる血中オキシステロール並びにリゾスフィンゴミエリン測定の診断の意義2016
- Author(s)
  衞藤義勝，岩本武夫，チェンウー，高村歩美，藤崎美和，柏崎雅代，衞藤　薫，酒井規夫
- Organizer
  第58回日本小児神経学会学術集会（2016，6.　3-5　東京
- Place of Presentation
  東京
- Year and Date
  2016-06-03
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] セベリパーゼアルファの小児及び成人ライソゾーム酸性リパーゼ欠損症における長期安全性成績2016
- Author(s)
  天野克之、衞藤義勝
- Organizer
  第43回日本小児栄養消化器肝臓学会
- Place of Presentation
  茨城
- Year and Date
  2016-09-16
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] Plasma Oxysterol and Lysosphingomyelin-509 as Potential Biomarkers for Japanese Patients with Niemann-Pick C disease measured by Tandem MS and their Changes with Miglustat Treatment2016
- Author(s)
  ○Yoshikatsu Eto, Takeo Iwamoto, Ayumi Takamura, Miwa Fujisaki, Masayo Kashiwazaki , Kaoru Eto, Norio Sakai
- Organizer
  13th International Congress of Human Genetics.
- Place of Presentation
  京都
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] SPG11（Spastic Paraplegia）－著明な色素沈着を呈し Adrenoleukodystrophy（ALD）が疑われた症例2016
- Author(s)
  衞藤義勝, 板垣里奈, 柳沼恵子, 柳澤比呂子, 會田隆志, 関晴朗, 山本悌司,
- Organizer
  第58回日本先天代謝異常学会
- Place of Presentation
  東京
- Year and Date
  2016-10-27
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] ファブリー病～早期診断・早期治療の重要性～2015
- Author(s)
  衞藤義勝
- Organizer
  第57回日本小児神経学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-05-29
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] Real-world experience in the diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2):report from an international collaboration of Expererts,2015
- Author(s)
  Eto. Y
- Organizer
  International symposium on Benign Infantile Seizures
- Place of Presentation
  東京
- Year and Date
  2015-09-25
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] 治療可能な遺伝性神経疾患―ニーマンピック病C型―早期発見に向けて2015
- Author(s)
  衞藤義勝
- Organizer
  第51回中部日本小児科学会学術集会
- Place of Presentation
  名古屋
- Year and Date
  2015-08-23
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] Neuronal Ceroid Lipofuscinosis　(NCL) タイプＩ(PPT1欠損症)姉弟例並びにタイプII　(TPP1欠損症)女児例2015
- Author(s)
  衞藤義勝
- Organizer
  第29回日本小児脂質研究会
- Place of Presentation
  鳥取
- Year and Date
  2015-10-25
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] Neuronal ceroid lipofuscinosis-2( CNL-2) disease, a type of Battern disease caused by TPP1 enzyme deficiency:Current knowledge of the natural history from international experts.2015
- Author(s)
  Eto. Y
- Organizer
  International symposium on Benign Infantile Seizures
- Place of Presentation
  東京
- Year and Date
  2015-09-25
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] REAL-WORLD EXPERIENCE IN THE DIAGNOSIS OF NEURONAL CEROID LIPOFUSCINOSIS TYPE 2 (CLN2): REPORT FROM AN INTERNATIONAL COLLABORATION OF EXPERTS.2015
- Author(s)
  Eto. Y
- Organizer
  第57回日本先天代謝異常学会
- Place of Presentation
  大阪
- Year and Date
  2015-11-14
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] ニーマンピックC病のオキシステロール並びにLyso-SM-501による診断2015
- Author(s)
  衞藤義勝
- Organizer
  第29回日本小児脂質研究会
- Place of Presentation
  鳥取
- Year and Date
  2015-10-25
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] オキシステロールについてのまとめ2015
- Author(s)
  衞藤義勝
- Organizer
  第56回日本神経学会イブニングセミナー
- Place of Presentation
  新潟
- Year and Date
  2015-05-22
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] NEURONAL CEROID LIPOFUSCINOSIS-2 (CLN2) DISEASE, A TYPE OF BATTEN DISEASE CAUSED BY TPP1 ENZYME DEFICIENCY: CURRENT KNOWLEDGE OF THE NATURAL HISTORY FROM INTERNATIONAL EXPERTS.2015
- Author(s)
  Eto. Y
- Organizer
  第57回日本先天代謝異常学会
- Place of Presentation
  大阪
- Year and Date
  2015-11-14
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] ニーマンピックC病の非侵襲性診断法：オキシステロール並びにlysoSM測定の有用性2015
- Author(s)
  衞藤義勝
- Organizer
  第57回日本先天代謝異常学会
- Place of Presentation
  大阪
- Year and Date
  2015-11-12
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] 先天性ムコ多糖症の診断、治療に関する最近の進歩－早期発見のために小児保健関係者ができること－2014
- Author(s)
  衞藤義勝
- Organizer
  第61回日本小児保健協会学術集会
- Place of Presentation
  福島
- Year and Date
  2014-06-22
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] ファブリー病～早期診断・早期治療の重要性～2014
- Author(s)
  衞藤義勝
- Organizer
  第55回日本神経学会学術大会ランチョンセミナー
- Place of Presentation
  福岡
- Year and Date
  2014-05-23
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] Gaucher disease type 3 -Diagnosis and Treatment, The 16th Asia LSD Symposium –Two decedes of ERT2014
- Author(s)
  衞藤義勝
- Organizer
  Achievements and Challenging issues
- Place of Presentation
  韓国
- Year and Date
  2014-09-27
- Invited
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] ファブリー病最新の話題2014
- Author(s)
  衞藤義勝
- Organizer
  大阪オープンセミナー
- Place of Presentation
  大阪
- Year and Date
  2014-04-20
- Invited
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] 乾燥濾紙血を用いたライソゾーム酸性リパーゼ欠損症（LAL D）のハイリスクスクリーニング2014
- Author(s)
  藤崎美和，梅田稔子，辻　嘉代子，大橋十也，井田博幸，衞藤義勝
- Organizer
  第56回日本先天代謝異常学会
- Place of Presentation
  宮城
- Year and Date
  2014-11-14
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] Niemann Pick C(NPC)患者での血清オキシステロール測定の診断への有用性に関して2014
- Author(s)
  衞藤義勝，岩本武夫，藤崎美和，高村歩美，梅田稔子，辻　嘉代子，大橋十也，井田博幸，衞藤　薫，濱田悠介，新寶里子，近藤秀仁，苛原　香，酒井規夫
- Organizer
  第56回日本先天代謝異常学会
- Place of Presentation
  宮城
- Year and Date
  2014-11-13
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] iPS細胞を用いてのライソゾーム病の形態的検討2014
- Author(s)
  辻　嘉代子，河越しほ，樋口　孝，藤崎美和，梅田稔子，平山怜美，井田博幸，大橋十也，衞藤義勝
- Organizer
  第56回日本先天代謝異常学会
- Place of Presentation
  宮城
- Year and Date
  2014-11-14
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] 遺伝子治療の現状、稀少疾患創薬に向けて2014
- Author(s)
  衞藤義勝
- Organizer
  レット症候群シンポジウム
- Place of Presentation
  東京
- Year and Date
  2014-04-19
- Data Source
  KAKENHI-PROJECT-26461536
[Presentation] Anti-CD3 antibody reduces antibody formation and prevents lethal hypersensitivity reaction in enzyme replacement therapy for murinelysosomal storage diseases2011
- Author(s)
  Ohashi T, Iizuka S, Shimada Y, Eto Y, Ida H, Kobayashi H
- Organizer
  11th International Symposium on Lysosomal Storage Diseases
- Place of Presentation
  Madrid
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Anti-CD3 antibody reduces antibody formation and prevents lethal hypersensitivity reaction in enzyme replacement therapy for Pompe disease in mouse2011
- Author(s)
  Ohashi T, Iizuka S, Shimada Y, Ida H, Eto Y, Kobayashi H
- Organizer
  Annual Symposium of the Society for the Study of Inborn Errors of Metabolism
- Place of Presentation
  Geneva, Switzerland
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Anti-CD3 antibody reduces antibody formation and prevents lethal hypersensitivitv reaction in enzyme replacement therapy for murinelysosomal storage diseases2011
- Author(s)
  Ohashi T, Iizuka S, Shimada Y, Eto Y, Ida H, Kobayashi H
- Organizer
  11th International Symposium on Lysosomal Storage Diseases
- Place of Presentation
  Madrid, Spain(招待講演)
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] ライソゾーム病酵素補充療法における酵素製剤に対する免疫反応に関する研究2011
- Author(s)
  大橋十也、飯塚佐代子、嶋田洋太、樋口孝、井田博幸、衛藤義勝、小林博司
- Organizer
  第53回日本先天代謝異常学会
- Place of Presentation
  幕張
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Anti-CD3 antibody reduces antibody formation and prevents lethal hypersensitivity reaction in enzyme replacement therapy for murine lysosomal storage diseases2010
- Author(s)
  Ohashi T, Eto Y, All
- Organizer
  11^<th> European round table on FABRY DISEASE.
- Place of Presentation
  Istanbul, Turkey
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] ライソゾーム病の酵素補充療法における抗体産生2010
- Author(s)
  大橋十也、衛藤義勝
- Organizer
  第15回日本ライソゾーム病研究会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] 抗CD3抗体によるポンペ病酵素補充療法での酵素製剤に対する免疫寛容導入2010
- Author(s)
  大橋十也, 飯塚佐代子, 衛藤義勝, 嶋田洋太, 井田博幸, 小林博司
- Organizer
  第52回日本先天代謝異常学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] 日本人Fabry病家系の遺伝子変異についての研究遺伝子変異と臨床病型について2010
- Author(s)
  小林正久、大橋十也、井田博幸、衞藤義勝
- Organizer
  日本先天代謝異常学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] 新生児MPS VIIマウスへの遺伝子治療におけるレンチウイルスベクタの長期発現2010
- Author(s)
  有賀賢典、小林博司、飯塚佐代子、金城栄子、清水寛美、衞藤義勝、大橋十也、井田博幸
- Organizer
  日本先天代謝異常学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] MPSII型Knockoutマウスでの脳室内酵素治療に関する研究2010
- Author(s)
  樋口孝、清水寛美、河越しほ、福田隆浩、小林博司、井田博幸、大橋十也、平戸徹、西野勝哉、衞藤義勝
- Organizer
  日本先天代謝異常学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] 濾紙血を用いたPompe病スクリーニング法の有用性と問題点2010
- Author(s)
  清水寛美、嶋田洋太、若林太一、小林博司、大橋十也、井田博幸、川井充、衞藤義勝
- Organizer
  日本先天代謝異常学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] ポンペ病細胞におけるオートファジー活性化の分子機序2010
- Author(s)
  嶋田洋太、西山由梨佳、小林博司、衞藤義勝、井田博幸、大橋十也
- Organizer
  日本先天代謝異常学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] ファブリ病モデルマウスに対する骨髄移植におけるキメリズムの決定2010
- Author(s)
  横井貴之、小林博司、衞藤義勝、石毛信之、北川照男、大津真、中内啓光、大橋十也、井田博幸
- Organizer
  日本先天代謝異常学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Immune tolerance induction in enzyme replacement therapy for Pompe disease by anti-CD3 antibody and oral enzyme administration.2009
- Author(s)
  Ohashi T, Iizuka S, Eto Y, Ida H.
- Organizer
  The 59^<th> Annual Meeting The American Society of Human Genetics
- Place of Presentation
  Honolulu, Hawaii
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Pompe病酵素補充療法における酵素製剤に対する免疫寛容導入法の開発2009
- Author(s)
  大橋十也、飯塚佐代子、衛藤義勝、井田博幸
- Organizer
  日本人類遺伝学会第54回大会
- Place of Presentation
  東京
- Year and Date
  2009-09-02
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Impact of Antibody Formation for Enzyme Replacement Therapy for Lysosomal Storage Diseases and Immune Tolerance Induction for Infused Enzyme2009
- Author(s)
  Ohashi T, Iizuka S, Eto Y, Ida Y
- Organizer
  11th InternationalCongress on Inborn Errors of Metabolism
- Place of Presentation
  San Diego, USA
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Immune tolerance induction in enzyme replacement therapy for Pompe disease by anti-CD3 antibody and oral enzyme administration2009
- Author(s)
  Ohashi T, Iizuka S, Kobayashi H, Shimada Y, Eto Y, Ida Y
- Organizer
  The 3th Internationl Symposium of Lysosomal Storage Diseases
- Place of Presentation
  Nagoya
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Pompe病の酵素補充療法における酵素製剤に対する免疫寛容導入2009
- Author(s)
  大橋十也、飯塚佐代子、嶋田洋太, 小林博司, 衞藤義勝, 井田博幸
- Organizer
  第51回日本先天代謝異常学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Impact of Antibody Formation for Enzyme Replacement Therapy for Lysosomal Storage Diseases and Immune Tolerance Induction for Infused Enzyme.2009
- Author(s)
  Ohashi T, lizuka S, Eto Y, Ida H.
- Organizer
  11^<th> International Congress on Inborn Errors of Metabolism
- Place of Presentation
  San Diego, USA
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Immune tolerance induction in enzyme replacement therapy for Pompe disease by anti-CD3 antibody and oral enzyme administration2009
- Author(s)
  Ohashi T, Iizuka S, Eto Y, Ida Y
- Organizer
  59th Annual Meeting The American Society of Human Genetics
- Place of Presentation
  Honolulu, Hawaii
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] Immune tolerance induction in enzyme replacement therapy for Pompe disease by anti-CD3 antibody and oral enzyme administration.2009
- Author(s)
  Ohashi T, lizuka S, Kobayashi H, Shimada Y, Eto Y, Ida H.
- Organizer
  The 3^<th> Internationl Symposium of Lysosomal Storage Diseases.
- Place of Presentation
  Nagoya
- Data Source
  KAKENHI-PROJECT-21591333
[Presentation] 先天性代謝異常症の酵素補充療法2008
- Author(s)
  衛藤義勝
- Organizer
  第3回千葉先天代謝異常学会
- Place of Presentation
  千葉
- Year and Date
  2008-07-11
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] Novel Treatment for Genetic Diseases2008
- Author(s)
  Eto Y
- Organizer
  Shanghai International Congress Of Pediatrics
- Place of Presentation
  Shanghai
- Year and Date
  2008-10-16
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] Recent Advances of the Treatment of Genetic Diseases2008
- Author(s)
  Eto Y
- Organizer
  The 28th Congress of Vietnum society of Pediatrics
- Place of Presentation
  Hochi Mihn
- Year and Date
  2008-12-28
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] Fabry病Up Date2008
- Author(s)
  衛藤義勝
- Organizer
  新潟ファブリ病研究会
- Place of Presentation
  新潟
- Year and Date
  2008-09-14
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] Current Status of Japanese Pediatric Problems2008
- Author(s)
  Eto Y
- Organizer
  International Symposium of Pediatrics, Asan University Medical School
- Place of Presentation
  Korea
- Year and Date
  2008-07-06
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] Recent Advances of Enzyme Replacement Therapy for Lysosomal Storage Disease.2008
- Author(s)
  Eto Y
- Organizer
  HUGO meeting
- Place of Presentation
  Sebu Island
- Year and Date
  2008-04-02
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] ファブリ病の酵素補充療法最近の進歩2008
- Author(s)
  衛藤義勝
- Organizer
  ファブリ病患者会
- Place of Presentation
  東京
- Year and Date
  2008-05-17
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] 先天代謝異常症の治療の最近の進歩2008
- Author(s)
  衛藤義勝
- Organizer
  東北小児成長研究会
- Place of Presentation
  郡山
- Year and Date
  2008-09-20
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] New Strategy for the Treatment of Genetic Disease2007
- Author(s)
  衛藤義勝
- Organizer
  The 24^<th> International Congress of Pediatrics
- Place of Presentation
  Athens, Greece
- Year and Date
  2007-09-01
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] ファブリ病の酵素補充療法-最近の進歩2007
- Author(s)
  衛藤義勝
- Organizer
  住友ファブリ病フォーラム
- Place of Presentation
  東京
- Year and Date
  2007-09-30
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] Current Status of Enzyme Replacement Therapy of LSD in Japan2007
- Author(s)
  衛藤義勝
- Organizer
  International Symposium of LSD
- Place of Presentation
  舞浜
- Year and Date
  2007-11-29
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] ファブリ病の酵素補充療法-最近の進歩2007
- Author(s)
  衛藤義勝
- Organizer
  第28回日本小児脂質研究会
- Place of Presentation
  東京
- Year and Date
  2007-12-08
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] Current Status of Enzyme Replacement Therapy of LSD in Japan,2007
- Author(s)
  衛藤義勝
- Organizer
  nternational Symposium of LSD,
- Place of Presentation
  舞浜
- Year and Date
  2007-11-29
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] ファブリ病の最近の進歩2007
- Author(s)
  衛藤義勝
- Organizer
  東日本皮膚科学会
- Place of Presentation
  札幌
- Year and Date
  2007-09-23
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] ファブリ病の酵素治療の進歩2007
- Author(s)
  衛藤義勝
- Organizer
  第52回日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] New Strategy for the Treatment of Genetic Disease,2007
- Author(s)
  衛藤義勝
- Organizer
  The 24th International Congress of Pediatrics,
- Place of Presentation
  Athens, Greece
- Year and Date
  2007-09-01
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] ファブリ病の酵素治療の進歩2007
- Author(s)
  衛藤義勝
- Organizer
  第52回日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-19591223
[Presentation] 免疫寛容導入による効果的ポンペ病酵素補充療法の開発
- Author(s)
  大橋十也　嶋田洋太　樋口孝　飯塚佐代子　井田博幸　衞藤義勝　小林博司
- Organizer
  第56回日本先天代謝異常学会
- Place of Presentation
  仙台
- Year and Date
  2014-11-13 – 2014-11-15
- Data Source
  KAKENHI-PROJECT-24591526

1. IDA Hiroyuki (90167255)

# of Collaborated Projects: 24 results

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2. OHASHI TOYA (60160595)

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3. TOKORO T. (40112841)

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13. 岩澤京子 (10301524)

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14. GOMIBUCHI Ichizou (50205621)

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15. SASAKI Nobuhiko (50170684)

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16. KAWAME H. (60246395)

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17. KOBAYASHI Masahisa (20312019)

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18. MIYATA Ichiro (10200180)

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19. TAHARA Takahiro (80159029)

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20. 柳澤比呂子 (60416659)

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21. HOSSAIN ARIF (40777893)

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22. GIESELMANN V

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23. TAJIMA Asako (00328337)

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24. SHIMADA Yohta (20560824)

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25. HIGUCHI Takashi (30595327)

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26. SAKURAI S. (20056542)

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27. KUSANO Kaoru (80205070)

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28. SUGIMOTO M (90206433)

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29. SUGAMA Seiichi (10154452)

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30. KUROSAWA Kenji (20277031)

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31. TANAKA T (50110929)

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32. OKAMOTO Aikou (20204026)

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33. TAKEYUKI Misawa (50260956)

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34. SUZUKI Satosi (70246940)

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35. TAKEYAMA Hirosi (70236511)

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36. SIMADA Takasi (20125074)

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37. SUZUKI Hideaki (20206519)

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38. YOSHIKAWA Hideki (60328367)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
39. NOZAKI Kazuyuki (80312023)

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40. KANAMOTO Yurie (80130160)

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41. TADA Yuki (10179707)

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42. SEKIGUCHI Shigeru (90119818)

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44. 岡田伸太郎 (30028609)

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55. BARRANGER J.a.

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56. BRADY R.d.

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58. BARRANGER J.

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60. 野呂拓史

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61. 高村歩美

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62. 渡部和彦

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Eto Yoshikatsu 衞藤 義勝

衞藤 義勝 エトウ ヨシカツ

ETO Yoshikatsu 衞藤 義勝

ETO Y. 衛藤 義勝

Research Projects

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Co-Researchers

Pathological analysis and drug screening using iPS cells derived from Fabry disease patientsPrincipal Investigator

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Pathogenesis, Diagnosis and treatment of lysosomal diseases by Biomarker AnalysisPrincipal Investigator

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Pathogenetic Stidies and Novel Enzyme Treatment using Fabry, Pompe and Tay-Sacks iPS cellsPrincipal Investigator

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Anti-CD3 antibody induced immune tolerance to infused enzyme in enzyme replacement therapy for lysosomal storage diseasePrincipal Investigator

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Immune tolerance induction in enzyme replacement therapy for lysosomal storage diseasesPrincipal Investigator

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Principal Investigator

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Development of novel therapy and elucidation of pathophysiology for genetic leukodystrophyPrincipal Investigator

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Molecular Pathogenesis of Brain Damage and Gene Therapy in Genetic LeukodystrophyPrincipal Investigator

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Prenatal Diagnosis of Ingenited Metabolic Disorders Using Maternal BloodPrincipal Investigator

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Eto Yoshikatsu 衞藤義勝

衞藤義勝エトウヨシカツ

ETO Yoshikatsu 衞藤義勝

ETO Y. 衛藤義勝