• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

NONAKA Ikuya  埜中 征哉

ORCIDConnect your ORCID iD *help
Researcher Number 80040210
Affiliation (based on the past Project Information) *help 2010: 独立行政法人 国立精神・神経医療研究センター, 病院, 名誉院長
2006 – 2008: 国立精神・神経センター, 神経研究所, 名誉所員
2007: National Institute of Neuroscience, Honorary member
2006: 国立精神・神経センター, 神経研究所, 名誉職員
1999: 国立精神・神経センター, 神経研究所・微細構造研究部, 部長 … More
1997 – 1998: 国立精神, 神経センター・神経研究所・微細構造研究部, 部長
1996: National Center of Neurology and Psychiatry, Ultrastructural Research, Director, 神経研究所・微細構造研究部, 部長
1996: Division of Ultrastructural Research, National Institute of Neuroscience, Nation, 武蔵病院・臨床検査部, 部長
1995: 国立精神・神経センター, 微細構造研究部, 部長
1995: 国立精神神経センター, 武蔵病院臨床検査部, 部長
1994: 国立精神神経センター, 武蔵病院, 部長
1991 – 1994: 国立精神, 神経センター・神経研究所・微細構造研究部, 部長
1993: 国立遺伝学研究所, 国立精神・神経センター神経研究所・微細構造研究部, 部長
1991 – 1993: National Institute of Neuroscience, NCNP, Division of Ultrastructural Research, Head, 神経研究所・微細構造研究部, 部長
1992: 国立精神神経センター, 神経研究所微細構造研究部, 部長
1991: 国立精神神経センター, 神経研究所・微細構造研究部, 部長
1990: 国立精神・神経センター, 神経研究所・微細構造研究城, 部長
1989: National Institute of Neuroscience, Head, ・神経研究所微細構造研究部, 部長
1987 – 1989: Division of Ultrastructural Research,National Institute of Nauroscience,NCNP, 神経研究所・微細構造研究部, 部長
1987: 国立精神神経センター, 神経研究所・微細構造研究部
1986: 国立精神, その他, その他
1986: NCNP, National Institute of Neuroscience, Division of Ultrastructural Research,, 神経研究所・微細構造研究部, 部長 Less
Review Section/Research Field
Principal Investigator
Neurology / Pediatrics
Except Principal Investigator
Neurology / Neurology / Pediatrics
Keywords
Principal Investigator
ミトコンドリア脳筋症 / ミトコンドリアDNA / 組織特異性 / 筋生検 / ミトコンドリアミオパチ- / MELAS / ミトコンドリアミオパチー / メラス / Mitochondrial Myopathy / Mitochondrial DNA … More / 組織バンク / 複合体IV欠損 / 電顕組織化学 / ミトコンドリアミオパタ- / チトクロ-ムC酸化酵素 / ミトコンドリアDNA(mtDNA) / 慢性外眼筋麻痺症候群 / ミオクロヌスてんかん / チトクロム酸化酵素 / 慢性外眼麻痺症候群 / 慢性外眼筋麻痺 / MERRF / Cytochrome c Oxidase / Tissue Specificity / Chronic Progressive External Ophthalmoplegia / Myoclonus Epilepsy / ミトコンドリアDNA変異 / 進行性筋ジストロフィー / デュシャンヌ型 / ベッカー型 / ジストロフィン / 代謝性筋疾患 / 神経・筋疾患 / 進行性筋ジストロフィ- / 糖原病 / mitochondrial disease / mitochondrial DNA mutation / progressive muscular dystrophy / Duchenne type / Becker type / dystrophin / metabolic myopathy / ミトコンドリア アンギオパチー / Leigh 脳症 / 点変異 / 血層異常 / mitochondrial encephalomyopathies / mitochondrial DNA / Mitochondrial angiopathy / Tissue specificity / 縁取り空胞 / タウ蛋白 / アルツハイマー病 / アミロイドβ / アミロイドβ前駆体蛋白 / クロロキン / rimmed vacuole / β-アミロイド / チューブリン / 熱ショック蛋白70 / アポリポ蛋白E / rimmed vacuoles / tau / Alzheimmer's disease / beta-APP / myopathies / chloroquine / 電子伝達系酵素欠損 / 筋病理 / Mitochondrial myopathy / Derect in electron transport system / Muscle biopsy / 細胞バンク / 神経 / 筋 / 診断 / ミトコンドリア脳筋性 / Cell Bank / Tissue Bank / Neuron / Muscle / Diagnosis / 慢性進行性外眼筋麻痺 / 複合体IV部分欠損 / 神経筋疾患 / 組織培養 / Mitochondrial myopathies / Chronic Progressive Ophthalmoplegia / Focal Complex IV Deficiency / Neuromuscular Diseases … More
Except Principal Investigator
ミトコンドリア脳筋症 / ミトコンドリアDNA / ヘテロプラスミィー / ミトコンドリア / トランスジェニックマウス / mtDNA / ミトコンドリア病 / mdx mice / DMD / IL-6 / ZASP / myotilin / CK / LDH / 慢性外眼筋麻痺症候群 / 塩基配列 / DNA診断 / 点突然変異 / tRNA / PCR / ミスマッチプライマー / 核膜 / 筋ジストロフィー / 臨床 / 遺伝子 / 細胞・組織 / 病理 / シグナル伝達 / 脳神経疾患 / マクロアレイ / マイクロマレイ / 神経分子病態学 / 筋疾患 / オートファジー / 神経分子病態 / 培養細胞 / データベース / 細胞バンク / ミトコンドリアサイドパチ- / 培養 / 筋細胞 / HeLa細胞 / MITOCHONDRIA / CULTURED CELLS / DATABASE / CELL BANK / 転移RNA / 遺伝子導入 / トランスジュニックマウス / Mitochondria / Mitochondrial DNA / Mitochondrial encephalomyopathy / Transfer RNA / Transgenic Mouse / Gene transfer / ミトコンドリア遺伝子疾患 / mtDNA導入 / ミトコンドリアノックアウトマウス / 疾患モデルマウス / マウスmtDNA / mtDNA突然変異 / mtDNA欠損細胞 / 病態モデルマウス / シナプトゾーム / 老化 / 糖尿病 / mitochondrial diseases / mtDNA inlroduction / mitochondrial KO mice / disease-model mice / こはく酸脱水素酵素 / フラボプロテイン / 複合体II / 分子遺伝学 / 先天代謝異常 / フラビンタンパク / 鉄-イオウ蛋白 / cDNA / 電子伝達系 / succinate dehydrogenase / flavoprotein / complex II / molecular genetics / inborn error of metabolism / mitochondrial disease / 基底膜 / メロシン / 先天性筋ジストロフィー / dy3Kマウス / MHC IIB / アポトーシス / 筋再生 / インテグリン / ラミニン / myosin IIB chain / ノックアウトマウス / alphaジストログリカン / merosin-deficient congenital muscular dystrophy / merosin / laminin α2 chain / dy^<3K> / dy^<3K>mice / laminin M chain / apoptosis / αdystroglycan / integrin / ユートロフィン / ジストロフィン / アデノウイルスベクター / mRNAの安定化 / サイトカイン / 免疫応答 / 炎症反応 / 免疫反応 / utrophin / dystrophin / adenovirus vector / stabilization of mRNA / cytokines / 神経・筋疾患 / サルコメア / カルパイン3 / cDNAマイクロアレイ / 筋原線維性ミオパチー / ミオティリン / 肢帯型筋ジストロフィー / 臨床遺伝学 / ミオフィブリラーミオパチー / マルチミニコア / 拡張型心筋症 / 分子病理学 / ミオフィプリラーミオパチー / Neuromuscular disorders / sarcomere / calpain 3 / cDNA microarray / myofibrillar myopathy / limb-girdle muscular dystrophy / 無血清培地 / 筋培養 / Thy-1抗原 / 細胞表面抗原 / Chemically defiened serum free culture medium / Muscle culture / Thy-1 antigens Less
  • Research Projects

    (20 results)
  • Research Products

    (24 results)
  • Co-Researchers

    (28 People)
  •  Elucidation of pathomechanism of and development of therapy ofautophagy-related muscle disorders

    • Principal Investigator
      NISHINO Ichizo
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Clinical and molecular studies of Emery-Dreifuss muscular dystrophy

    • Principal Investigator
      HAYASHI Yukiko
    • Project Period (FY)
      2006 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Clarification of pathomechanism of inherited muscular disorder due to abnormality of sarcomeric proteins

    • Principal Investigator
      MINAMI Narihiro
    • Project Period (FY)
      2006 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Elucidation of molecular mechanism of utrophin expression in dystrophic skeletal muscle and its application to molecular therapy

    • Principal Investigator
      TAKEDA Shin'ichi
    • Project Period (FY)
      1999 – 2001
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Neurology
    • Research Institution
      National Institute of Neuroscience, NCNP
  •  Elucidation of Molecular Mechanism of Muscle Degenaration using Developmental Biology Technique and development of therapeutics

    • Principal Investigator
      TAKEDA Shin'ichi
    • Project Period (FY)
      1998 – 2000
    • Research Category
      Grant-in-Aid for Scientific Research (B).
    • Research Field
      Neurology
    • Research Institution
      National Institute of Neuroscience, NCNP
  •  Molecular genetic study of succinate dehydrogenase deficiency

    • Principal Investigator
      GOTO Yu-ichi
    • Project Period (FY)
      1997 – 1998
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Institute of Neuroscience National Center of Neurology and Psychiatry (NCNP)
  •  An experimental study to explore the pathogenetic mechanism of senile plaque formation and neurofibrillar degeneration in Alzheimer's diseasePrincipal Investigator

    • Principal Investigator
      NONAKA Ikuya
    • Project Period (FY)
      1995 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Isolation of mtDNA knock-out mice by introduction of disease-related mtDNA mutation

    • Principal Investigator
      HAYASHI Jun-ichi
    • Project Period (FY)
      1994 – 1996
    • Research Category
      Grant-in-Aid for Scientific Research (A)
    • Research Field
      Neurology
    • Research Institution
      University of Tsukuba
  •  ミトコンドリア病におけるDNA診断法の開発と病態の解明

    • Principal Investigator
      宝来 聴
    • Project Period (FY)
      1993
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      National Institute of Genetics
  •  Study on gene abnormality of mitochondrial encephalomyopathy and development of its transgenic mouse

    • Principal Investigator
      GOTO Yuichi
    • Project Period (FY)
      1993 – 1994
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry
  •  ミトコンドリア病におけるDNA診断と病態の解明

    • Principal Investigator
      HORAI Satoshi
    • Project Period (FY)
      1992 – 1993
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      National Institute of Genetics
  •  MECHANISMS OF EXPRESSION OF DELETED MITOCHONDRIAL DNA FROM CULTURE CELLS

    • Principal Investigator
      KIKUCHI Aiko
    • Project Period (FY)
      1992
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      NATIONAL CENTER OF NEUROLOGY AND PSYCHIATRY
  •  A study on tissue expression from mitochondrial DNA mutationsPrincipal Investigator

    • Principal Investigator
      NONAKA Ikuya
    • Project Period (FY)
      1992 – 1993
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP)
  •  Establishment of diagnostic networks and DNA bank for neuromuscular disordersPrincipal Investigator

    • Principal Investigator
      NONAKA Ikuya
    • Project Period (FY)
      1991 – 1992
    • Research Category
      Grant-in-Aid for Co-operative Research (A)
    • Research Field
      Neurology
    • Research Institution
      National Institute of Neuroscience, National Center of Neurology and Psychiatry (NCNP)
  •  Mitochondrial DNA mutations and tissue specificity in mitochondrial myopathiesPrincipal Investigator

    • Principal Investigator
      NONAKA Ikuya
    • Project Period (FY)
      1990 – 1991
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Institute of Neuroscience, NCNP
  •  A molecular biologic study on pathogenesis of neuromuscular diseases with mitochondrial enzyme defectsPrincipal Investigator

    • Principal Investigator
      NONAKA Ikuya
    • Project Period (FY)
      1988 – 1989
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psychiatry (NCNP)
  •  ミトコンドリア電子伝達系異常の診断法の確立と培養細胞による発症機序の解明Principal Investigator

    • Principal Investigator
      埜中 征哉
    • Project Period (FY)
      1987
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Research Institution
      National Center of Neurology and Psychiatry
  •  Development of cell bank and assay kit for human neural and muscular disorders: Application to genetic engineeringPrincipal Investigator

    • Principal Investigator
      NONAKA Ikuya
    • Project Period (FY)
      1987 – 1989
    • Research Category
      Grant-in-Aid for Developmental Scientific Research
    • Research Field
      Pediatrics
    • Research Institution
      National Center of Neurology and Psychiatry (NCNP)
  •  A study for diagnosis and pathophysiology in neuromuscular disorders due to mitochondrial enzyme defectsPrincipal Investigator

    • Principal Investigator
      NONAKA Ikuya
    • Project Period (FY)
      1986 – 1987
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Institute of Neuroscience,NCNP
  •  Establishment of a serum free medium for human muscle cells and its application of studyefor muscle disease

    • Principal Investigator
      KIKUCHI Aiko
    • Project Period (FY)
      1985 – 1986
    • Research Category
      Grant-in-Aid for General Scientific Research (C)
    • Research Field
      Neurology
    • Research Institution
      National Center of Neurology and Psyciatry (NCNP)
      国立武蔵療養所

All 2010 2009 2008 2007 2006

All Journal Article Presentation

  • [Journal Article] Autophagic degradation of nuclear components in mammalian cells2009

    • Author(s)
      Park YE, Hayashi YK, Bonne G, Arimura T, Noguchi S, Nonaka I, Nishino I
    • Journal Title

      Autophagy 5

      Pages: 795-804

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Danon 病患者17家系51例における心筋障害の臨床的特徴2009

    • Author(s)
      杉江和馬, 埜中征哉, 西野一三
    • Journal Title

      心臓 41

      Pages: 413-418

    • NAID

      130003376912

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Autophagic degradation of nuclear components in mammalian cells2009

    • Author(s)
      Park YE, Hayashi YK, Bonne, G, Arimura T, Noguchi S, Nonaka I, Nishino I.
    • Journal Title

      Autophagy 5巻(in press)

      Pages: 0-0

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI2009

    • Author(s)
      Murakami T, Hayashi YK, Ogawa M, Noguchi S, Campbell KP, Togawa M, Inoue T, Oka A, Ohno K, Nonaka I, Nishino I
    • Journal Title

      Brain Dev 31巻

      Pages: 465-468

    • NAID

      10025580402

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B2009

    • Author(s)
      Park YE, Hayashi YK, Goto K, Komaki H, Hayashi Y, Inuzuka T, Noguchi S, Nonaka I, Nishino I.
    • Journal Title

      Neuromuscul Disord 19巻

      Pages: 29-36

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Novel FHL1 mutations in fatal and benign reducing body myopathy2009

    • Author(s)
      Shalaby S, Hayashi YK, Nonaka I, Noguchi S, Nishino I
    • Journal Title

      Neurology 72巻

      Pages: 375-376

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Danon病患者17家系51例における心筋障害の臨床的特徴2009

    • Author(s)
      杉江和馬,埜中征哉,西野一三
    • Journal Title

      心臓 41

      Pages: 413-418

    • NAID

      130003376912

    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Congenital myotonic dystrophy can show congenital fiber type disproportion pathology2009

    • Author(s)
      Tominaga, Hayashi YK, Goto K, Minami N, Noguchi S, Nonaka I, Miki T, Nishino I
    • Journal Title

      Acta Neuropathol 119

      Pages: 481-486

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions2008

    • Author(s)
      Yamashita S, Nishino I, Nonaka I, Goto Y
    • Journal Title

      J Hum Genet 53

      Pages: 598-606

    • NAID

      10021249625

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Journal Article] Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1)2008

    • Author(s)
      Shalaby S, Hayashi YK, Goto K, Ogawa M, Nonaka I, Noguchi S, Nishino I.
    • Journal Title

      Neuromuscul Disord 18巻

      Pages: 959-961

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan2007

    • Author(s)
      Astejada, MN, Goto K, Nagano A, Ura S, Noguchi S, Nonaka I, Nishino I, Hayashi YK
    • Journal Title

      Acta Myol 26巻

      Pages: 159-164

    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Limb-girdle muscular dystrophy due to emerin gene mutations2007

    • Author(s)
      Ura S, Hayashi YK, Goto K, Astejada MN, Murakami T, Nagato M, Ohta S, Daimon Y, Takekawa H, Hirata K, Nonaka I, Noguchi S, Nishino I
    • Journal Title

      Archives of neurology 64巻

      Pages: 1038-1041

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Journal Article] Emerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles2006

    • Author(s)
      Ozawa R, Hayashi YK, Ogawa M, Kurokawa R, Matsumoto H, Noguchi S, Nonaka I, Nishino I
    • Journal Title

      Am J Pathol 168巻

      Pages: 907-917

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-18390265
  • [Presentation] A case of X-linked myopathy with excessive autophagy : the first case in Japan2010

    • Author(s)
      Kurashige T, Takahashi T, Kondo K, Nakamura T, Yamawaki T, Tsuburaya R, Hayashi YK, Nonaka I, Nishino I, Matsumoto M
    • Organizer
      15th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Kumamoto, Japan
    • Year and Date
      2010-10-13
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Genetic, clinical, and pathological features of congenital fiber type disproportion in Japan2010

    • Author(s)
      Tominaga K, Hayashi YK, Goto K, Minami N, Noguchi S, Nonaka I, Miki T, Nishino I
    • Organizer
      15th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Kumamoto, Japan
    • Year and Date
      2010-10-13
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Congenital myotonic dystrophy in patients diagnosed as congenital fiber type disproportion2009

    • Author(s)
      Tominaga K, Hayashi YK, Goto K, Minami N, Noguchi S, Nonaka I, Nishino I
    • Organizer
      14th International Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Geneva, Switzerland
    • Year and Date
      2009-09-11
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Approach to distal myopathies(遠位型ミオパチーへのアプローチ)2009

    • Author(s)
      埜中征哉
    • Organizer
      アジア・オセアニア筋学センター(AOMC)第8回年次総会
    • Place of Presentation
      The Leela Kempinski(インド ムンバイ)
    • Year and Date
      2009-05-23
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Sialic acid metabolites preclude the development of myopathic phenotype in the DMRV/hIBM mouse model2009

    • Author(s)
      Malicdan MCV, Noguchi S, Hayashi YK, Nonaka I, 他
    • Organizer
      第14回世界筋学会国際会議(WMS)
    • Place of Presentation
      UNI-MAIL(スイス ジュネーブ)
    • Year and Date
      2009-09-09
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Sialic acid metabolites preclude the development of myopathic phenotype in the DMRV/hIBM mouse model2009

    • Author(s)
      Malicdan MCV, Noguchi S, Hayashi YK, Nonaka I, Nishino I
    • Organizer
      Congress of the World Muscle Society (WMS)
    • Place of Presentation
      Geneva, Switzerland
    • Year and Date
      2009-09-09
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Approach to distal myopathies(遠位型ミオパチーへのアプローチ)2009

    • Author(s)
      埜中征哉
    • Organizer
      アジア・オセアニア筋学センター(AOMC)第8回年次総会
    • Place of Presentation
      インド(ムンバイ)
    • Year and Date
      2009-05-23
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Cytoplasmic body with acid phosphatase activity-Hallmark of adult-onset Pompe disease on muscle pathology2008

    • Author(s)
      Nishino I, Oya Y, Monma K, Noguchi S, Hayashi YK, Nonaka I
    • Organizer
      Congress of the World Muscle Society (WMS), Newcastle Upon Tyne
    • Place of Presentation
      United Kingdom
    • Year and Date
      2008-10-01
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Becker型筋ジストロフィーにおける縁取り空胞の出現に関する臨床病理学的検討2008

    • Author(s)
      門間一成,野口悟,林由起子,南成祐,元吉和夫,鎌倉恵子,埜中征哉,西野一三
    • Organizer
      第49回日本神経学会総会
    • Place of Presentation
      横浜
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Novel ETFDH mutations and normal CoQ10 level in Taiwanese patients with multiple acyl-CoA dehydrogenase deficiency2008

    • Author(s)
      Liang WC, Ohkuma A, Hayashi YK, Lopez LC, Hirano M, Nonaka I, Noguchi S, Jong YJ, Nishino I
    • Organizer
      Congress of the World Muscle Society (WMS), Newcastle Upon Tyne
    • Place of Presentation
      United Kingdom
    • Year and Date
      2008-09-30
    • Data Source
      KAKENHI-PROJECT-20390250
  • [Presentation] Congenital myotonic dystrophy and myotubular myopathy may be differentiated by type 2C fibers and peripheral halos2008

    • Author(s)
      Fujimura C, Noguchi S, Minami N, Nonaka I, Hayashi YK, Nishino I
    • Organizer
      Congress of the World Muscle Society (WMS), Newcastle Upon Tyne
    • Place of Presentation
      United Kingdom
    • Year and Date
      2008-10-01
    • Data Source
      KAKENHI-PROJECT-20390250
  • 1.  KIKUCHI Aiko (70159010)
    # of Collaborated Projects: 7 results
    # of Collaborated Products: 0 results
  • 2.  GOTO Yuichi (20225668)
    # of Collaborated Projects: 7 results
    # of Collaborated Products: 0 results
  • 3.  NISHINO Ichizo (00332388)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 21 results
  • 4.  HORAI Satoshi (40126157)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 0 results
  • 5.  KMO Isao (70108489)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 0 results
  • 6.  HAYASHI Yukiko (50238135)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 19 results
  • 7.  NOGUCHI Satoru (00370982)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 18 results
  • 8.  TAKEDA Shin'ichi (90171644)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 9.  AIKAWA Hisashi (30184013)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 10.  MATSUOKA Taro
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 11.  SUGIE Hideo (60119980)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 12.  KOBAYASHI Masanori (50170353)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  ARAHATA Kiichi (30053325)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 14.  HAYASHI Jun-ichi (60142113)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 15.  HANAOKA Kazunori (40189577)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 16.  MINAMI Narihiro (20392417)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  SEGAWA Kaoru (30114523)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 18.  FURUKAWA Shoei (90159129)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  FURUKAWA Yoshiko (20219108)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  HONDA Shinya
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  TOMINAGA Kayo
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 22.  MONMA Kazunari
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 23.  KIYONO Chieko
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 24.  SAKUTA Ryoichi
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 25.  KOBAYASHI Osamu
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 26.  SUZUKI Yuko
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 27.  古賀 靖敏
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 28.  宮越 友子
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results

URL: 

Are you sure that you want to connect your ORCID iD to this researcher?
* This action can be performed only by the researcher themselves.

この研究者とORCID iDの連携を行いますか?
※ この処理は、研究者本人だけが実行できます。

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi