FUJIEDA Kenji 藤枝憲二

Researcher Number	60173407
Other IDs
External Links
Affiliation (based on the past Project Information) *help	2000 – 2010: 旭川医科大学, 医学部, 教授 1998 – 2000: 北海道大学, 医学部・附属病院, 講師 1998: 北海道大学, 医学部付属病院, 講師 1997: 北海道大学, 医学部附属病院, 講師 1996: Department of Pediatrics, Hokkaido University School of Medicine. Assistant Prof, 医学部付属病院, 講師 … More 1994 – 1996: 北海道大学, 医学部・附属病院, 講師 1993: 北海道大学, 医学部・附属病院, 助手 1990 – 1992: 北海道大学, 医学部附属病院, 助手 1989: 北海道大学, 医学部付属病院, 助手 1989: Hokkaido University Medical Hospital, Instructor, 医学部附病院, 助手 1987 – 1988: Lecturer,Hospital Hokkaido University, 医学部附属病院, 助手 1986: 北海道大学, 医学部, 助手 Less
Review Section/Research Field	Principal Investigator Pediatrics / Pediatrics / Biological Sciences Except Principal Investigator Pediatrics / Embryonic/Neonatal medicine / Pediatrics / Public health/Health science / Obstetrics and gynecology / Ophthalmology
Keywords	Principal Investigator DAX-1 / リポイド過形成症 / 先天性副腎低形成症 / StAR / SOX9 / アンドロゲン受容体 / WT1 / yeast two-hybrid screening / 副腎低形成症 / 相互作用因子 … More / インスリン受容体遺伝子 / Leprechaunism(妖精症) / Hypospadias / Androgen receptor / Skin fibroblast / Male Pseudohermaphrodism / HY抗体 / 性腺機能 / Y染色体構造異常 / アンドロゲンレセプター / 皮膚線維芽細胞 / 尿道下裂 / 男性仮性半陰陽 / Forkhead transcription factor / Insulin / GH / Life Span / IGF / フォークヘッド転写因子 / インスリン / 成長ホルモン / 寿命 / Gonadotropin / Gene regulation / Gene exression / Congenital adrenal hypoplasia / Molecular enetics / 性腺機能低下症 / ゴナドトロピン / ゴナドロピン / 遺伝子制御 / 遺伝子発現 / 遺伝子変異 / 低身長 / GH生物学的活性 / GH1 / ルシフェラーゼアッセイ / Pit1β / CPHD / XY女性 / yeast two-hybridシステム / GPR54 / KAL1 / hypogonadotropic hypogonadism / Kallmann症候群 / リポイド渦形成症 / yeast two-hybridscreening / 性分化異常症 / AHC / StAR、DAX-1 / 先天性リポイド過形成症 / 性分化異常症(DSD) / Yeast Two-hybrid Screening / 外陰部異常 / 複合型ステロイド合成障害 / 先天性副腎皮質過形成症(CAH) / P450 oxidoreductase(POR) / SFI / Ad4BP / P450 oxidoreductase (POR) / 遺伝子多型 / 寡少精子症 / SBP / 精巣形成不全症 / アンドロゲン不応症 / Ad4BP-SF-1 / yeast two-hbrid screening / POR異常症 / Antley-Bixler症候群 / 先天性副腎過形成症 / 性分化異常症 (DSD) / P450scc / 遺伝子異変 / 副甲状腺機能低下症 / カルシウムセンサー受容体 / コレステロール移送 / 副腎 / StAR遺伝子 / 自己リン酸化能 / 部位特異的変異導入 / 3βhydroxysteroid dehydrogenase(3β-HSD)欠損症 / 21水酸化酵素欠損症 / 3β-HSD遺伝子 / P450c21遺伝子 / 遅発型 / 古典型 / 遺伝的異質性 / 副腎過形成症 / インスリン抵抗性 / 子宮内発育不全 … More Except Principal Investigator Angelman syndrome / Prader-Willi syndrome / histone acetylation / DNA methylation / epigenetics / imprinting / steroid hormone / RIP140 / DAX-1 / SF-1 / IDDM / 子宮内発育不全 / ゲノム / 医療・福祉 / Goitrous autoimmune thyroiditis(GAT) / Atrophic autoimmune thyroiditis(AAT) / Graves' disease / Cretinism / Thyroid-stimulation blocking antibody(TSBAb) / Thyroid stimulating antibody (TSAb) / TSH-binding inhibitor immunoglobulin(TBII) / TSH-receptor antibody / 一過性低T_4血症 / 一過性甲状腺機能低下症 / TSH受容体ブロッキング抗体 / 抗TSH抗体 / TSH結合阻害抗体(TBII) / 甲状腺刺激阻害抗体(TSBAb) / 甲状腺刺激抗体(TSAb) / 尿中ヨ-ド / バセドウ病 / クレチン症マススクリ-ニング / TSBAb / TSAb / TBII / 甲状腺腫性甲状腺炎 / 萎縮性甲状腺炎 / グレ-ブ病 / クレチン症 / 甲状腺刺激阻害抗体 / 甲状腺刺激抗体 / TSH受容体結合阻害抗体 / TSH受容体抗体 / growth fator / intrauterine growth retardation / genome / medical / gene / ハプロタイプ / 子宮内胎児発育遅延 / SNP / 遺伝的多い型 / type 1 insulin-like growth factor receptor / insulin-like growth factor II / insulin-like gorwth factor I / 胎児発育 / 成長因子 / 遺伝子 / Fat tissue / Transgenic mice / Leptin sensitivfity / Hypothalamus / Forkhead Transcription factor / Food intake / 脂肪組織 / トランスジェニックマウス / レプチン感受性 / 視床下部 / フォークヘッド転写因子 / 摂食 / United States of America / international cooperation on science / patent ductus arteriosus in premature infants / nitric oxide synthase / gene polymorphism / estrogen / nitric oxide / ductus arteriosus / 遺伝子多型 / アメリカ合衆国 / 国際情報交換 / 未熟児動脈管開存 / 一酸化窒素合成酵素 / 遺伝子多型性 / エストロゲン / 一酸化窒素 / 動脈管 / cytochrome P450 / congenital anomaly / immune function / Thyroid function / neurobehavioral development / risk assessment / Influence on future generation / endocrine disrupting chemicals / P450 / シトクロムP450 / 先天異常 / 免疫機能 / 甲状腺機能 / 神経発達 / リスク評価 / 次世代影響 / 内分泌かく乱化学物質 / Proder-Willi症候群 / ヒストンアセチル化 / DNAメチル化 / ゲノム刷り込み現象 / Prader-Willi症候群 / StAR protein binding protein / Endometrial Cancer / Ovary / StAr / Sp1 / endometrial carcinoma / AhR / CO-activator / ARPP16 / 黄体機能 / ステロイドホルモン / StAR蛋白質結合蛋白質 / 子宮内膜癌 / 卵巣 / StAR / cortisol / melatonin / circadian rhythm / blind patient / 血中メラトニン濃度 / 睡眠・覚醒障害 / 視力障害 / コーチゾール / メラトニン / 生体リズム / 視覚障害者 / Insulin resistant diabetes / rhIGF-1 / Insulin receptor gene / Leprechaunism / HLA-DQ gene / HLA-DR gene / DRB1遺伝子 / DQA1遺伝子 / DQB1遺伝子 / HLAーDR抗原 / HLAーDQ抗原 / IDDM(インスリン依存性糖尿病) / DIAMOND研究 / DERI研究 / HLAーDR抗原遺伝子 / HLAーDQ抗原遺伝子 / インスリン抵抗性糖尿病 / 合成IGF-I / インスリン受容体遺伝子 / HLA-DQ遺伝子 / HLA-DR遺伝子 / インマリン受容体遺伝子 / レプリコニズム / HLA-DQB1遺伝子 / HLA-DRB1遺伝子 / HLA-DR抗原 / HLA-DQ抗原 / HLA抗原 / 11β-hdroxsteroid dehdroenase type2 / 11β-hydroxysteroid dehydrogenase type2 / 新生児 / 胎児 / グルコルチコイド / 副腎機能 / グルココルチコイド Less

候補遺伝子解析並びにハプロタイプ解析による成長障害の成因の同定Principal Investigator
- Principal Investigator
  
  藤枝憲二
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
Impact of glucocorticoid exposure for fetus in fetal development and neonatal disease
- Principal Investigator
  
  NAGAYA Ken
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Asahikawa Medical College
Comprehensive investigation of etiology and pathophysiology of disorders of sex development(DSD)Principal Investigator
- Principal Investigator
  
  FUJIEDA Kenji
- Project Period (FY)
  2005 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
The association between fetal and postnatal growth and polymorphisms of insulin-like growth factors
- Principal Investigator
  
  NAGAYA Ken, 竹田津原野
- Project Period (FY)
  2005 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Asahikawa Medical College
Search for the novel etiology in disorders of sex development (DSD) caused by abnormalities of adrenal glands and gonads.Principal Investigator
- Principal Investigator
  
  FUJIEDA Kenji
- Project Period (FY)
  2004 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Asahikawa Medical College
The role of Foxo1 on the mechanism by which insulin signaling regulates food intake
- Principal Investigator
  
  YOSHIDA Makoto, NAKAE Jun
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
Analysis of molecular mechanism of GH effect on life spanPrincipal Investigator
- Principal Investigator
  
  FUJIEDA Kenji
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
The role of nitric oxide on the vascular tone of the ductus arteriosus
- Principal Investigator
  
  KAJINO Hiroki
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
Influence of endocrine disrupting chemicals on the health of future generation
- Principal Investigator
  
  KISHI Reiko
- Project Period (FY)
  2001 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Public health/Health science
- Research Institution
  HOKKAIDO UNIVERSITY
リポイド過形成症の病因としてのコレステロール側鎖切断酵素遺伝子異常の検索Principal Investigator
- Principal Investigator
  
  藤枝憲二
- Project Period (FY)
  2000
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Asahikawa Medical College
Molecular analysis of steroidogenesis in the field of obstetrics and gynecology
- Principal Investigator
  
  SUGAWARA Teruo
- Project Period (FY)
  2000 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Obstetrics and gynecology
- Research Institution
  HOKKAIDO UNIVERSITY
Reactivation of imprinted genes in Prader-Willi syndrome.
- Principal Investigator
  
  SAITOH Shinji
- Project Period (FY)
  2000 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  HOKKAIDO UNIVERSITY
機能獲得型カルシウムセンサー受容体異常に関する分子遺伝学的研究Principal Investigator
- Principal Investigator
  
  藤枝憲二
- Project Period (FY)
  1998
- Research Category
  
  Grant-in-Aid for Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Hokkaido University
STRUCTURE-FUNCTION ANALYSIS OF DAX-1 USING Molecular analysisPrincipal Investigator
- Principal Investigator
  
  FUJIEDA kenji
- Project Period (FY)
  1997 – 1999
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Hokkaido University
StAR遺伝子の構造と機能に関する研究-リポイド過形成症での分子遺伝学的研究-Principal Investigator
- Principal Investigator
  
  藤枝憲二
- Project Period (FY)
  1996
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hokkaido University
子宮内発育不全発症機序に関する分子生物学的研究-妖精症をモデルとしてPrincipal Investigator
- Principal Investigator
  
  藤枝憲二
- Project Period (FY)
  1995
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hokkaido University
THE STUDY ON CIRCADIAN RHYTHM ABNORMALITY IN BLIND PATIENTS
- Principal Investigator
  
  TAGAWA Yoshitsugu
- Project Period (FY)
  1995 – 1996
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Ophthalmology
- Research Institution
  HOKKAIDO UNIVERSITY
遅発型副腎過形成症の分子遺伝学的解析Principal Investigator
- Principal Investigator
  
  藤枝憲二
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hokkaido University
妖精症をモデルとした子宮内発育不全発症機序に関する分子生物学的研究Principal Investigator
- Principal Investigator
  
  藤枝憲二
- Project Period (FY)
  1993
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hokkaido University
THE STUDY OF PATHOGENESIS IN JUVENILE ONSET OF DIABETES MELLITUS MOLECULAR BIOLOGICAL STUDY
- Principal Investigator
  
  KAJII Naofumi, MATSUURA Nobuo
- Project Period (FY)
  1990 – 1992
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  HOKKAIDO UNIVERSITY
Analysis of TSH receptor antibody and studies of effects of it upon thyroid development and function.
- Principal Investigator
  
  MATSUURA Nobuo
- Project Period (FY)
  1987 – 1989
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Hokkaido University
Etiological study of male pseudohermaphradism - With the speical emphasis on hypospadias.Principal Investigator
- Principal Investigator
  
  FUJIEDA Kenji
- Project Period (FY)
  1986 – 1987
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hokkaido University

All 2009 2008 2007 2006 2005 2004 2003

All Journal Article Presentation Book

[Book] 先天性副腎過形成症、小児疾患診療のための病態生理2008
- Author(s)
  藤枝憲二
- Publisher
  東京医学社、小児内科
- Data Source
  KAKENHI-PROJECT-17390294
[Book] 先天性副腎過形成症、小児疾患診療のための病態生理(小児内科 40増刊号)2008
- Author(s)
  藤枝憲二
- Publisher
  東京医学社
- Data Source
  KAKENHI-PROJECT-16086202
[Book] 内分泌臨床分野での進歩性成熟異常症最近の進歩、Annual Review糖尿病・代謝・内分泌20072007
- Author(s)
  藤枝憲二
- Publisher
  金原出版
- Data Source
  KAKENHI-PROJECT-17390294
[Book] Annual Review糖尿病・代謝・内分泌20072007
- Author(s)
  藤枝憲二
- Publisher
  金原出版
- Data Source
  KAKENHI-PROJECT-17390294
[Book] 内分泌臨床分野での進歩性成熟異常症最近の進歩(Annual Review糖尿病・代謝・内分泌2007)2007
- Author(s)
  藤枝憲二
- Publisher
  金原出版
- Data Source
  KAKENHI-PROJECT-16086202
[Book] Annual Review糖尿病・代謝・内分泌20072007
- Author(s)
  藤枝憲二
- Publisher
  金原出版
- Data Source
  KAKENHI-PROJECT-16086202
[Book] 先天性副腎過形成症、先端医療シリーズ、34、小児科の新しい流れ(柳澤正義、衛藤義勝、五十嵐隆編集)2005
- Author(s)
  藤枝憲二、向井徳男、田島敏広
- Publisher
  先端医療技術研究所
- Data Source
  KAKENHI-PROJECT-16086202
[Book] 先天性副腎過形成症、先端医療シリーズ小児科の新しい流れ2005
- Author(s)
  藤枝憲二、向井徳男、田島敏広(柳澤正義、衛藤義勝、五十嵐隆)
- Publisher
  先端医療技術研究所
- Data Source
  KAKENHI-PROJECT-17390294
[Book] 3β-hydroxysteroid dehydrogenase deficiency. Encyclopedia of Endocrine Disease Vol. 22004
- Author(s)
  Fujieda K, Nakae J, Mukai T
- Publisher
  Academic Press (Martini L eds)
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] A novel heterozygous mutation of steroidogenic factor-1 (SF1/Ad4BP) gene (NR5A1) in a 46, XY disorders of sex development (DSD) patient without adrenal failure2009
- Author(s)
  Tajima T, Fujiwara F, Fujieda K
- Journal Title
  
  Endocr J. (In press)
- NAID
  10026914347
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Cytochrome P450 oxidoreductase deficiency: Identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients2009
- Author(s)
  Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, Ishii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K, Ogata T
- Journal Title
  
  J Clin Endocrinol Metab. (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] A novel heterozygous mutation of steroidogenic factor-1(SF-1/Ad4BP)gene(NR5A1)in a 462009
- Author(s)
  Tajima T, Fujiwara F, Fujieda K
- Journal Title
  
  XY disorders of sex development(DSD)patient without adrenal failure. Endocr J (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] A novel heterozygous mutation of steroidogenic factor-1 (SF-1/Ad4BP) gene (NR5A1) in a 46, XY disorders of sex development (DSD) patient without adrenal failure2009
- Author(s)
  Tajima T, Fujiwara F, Fujieda K
- Journal Title
  
  Endocr J (in press)
- NAID
  10026914347
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Ogata T : Cytochrome P450 oxidoreductase deficiency : Identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients2009
- Author(s)
  Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, Ishii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K
- Journal Title
  
  J Clin Endocrinol Metab (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 胎児・新生児期の副腎機能2009
- Author(s)
  長屋建、藤枝憲二
- Journal Title
  
  日本未熟児新生児学会誌 21
  
  Pages: 33-38
- NAID
  10025626201
- Data Source
  KAKENHI-PROJECT-20591295
[Journal Article] Cytochrome P450 Oxidoreductase Deficiency : Identificationand Characterization of Biallelic Mutations and Genotype-Phenotype Correlations in 35 Japanese Patients2009
- Author(s)
  Fukami M, Nishimura G, Homma K, Nagai T, Hanaki K, Uematsu A, Ishii T, Numakura C, Sawada H, Nakacho M, Kowase T, Motomura K, Haruna H, Nakamura M, Ohishi A, Adachi M, Tajima T, Hasegawa Y, Hasegawa T, Horikawa R, Fujieda K. Ogata T
- Journal Title
  
  J Clin Endocrinol Metab (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 先天性副腎低形成2008
- Author(s)
  藤枝憲二
- Journal Title
  
  日本内科学会誌 97
  
  Pages: 736-742
- NAID
  10021253855
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 性分化異常症の管理に関する合意見解、日本小児内分泌学会性分化委員会報告2008
- Author(s)
  緒方勤、堀川玲子、長谷川奉延、位田忍、向井徳男、安達昌功、有坂治、藤枝憲二
- Journal Title
  
  日本小児科学会雑誌 112
  
  Pages: 565-578
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations: mutant DAX-1 failed to repress steroidogenic acute regulatory protein(StAR)and luteinizing hormone beta-subunit gene promoter activity.2008
- Author(s)
  Okuhara K, Abe S, Kondo T, Fujita K, Koda N, Mochizuki H, Fujieda K, Tajima T
- Journal Title
  
  Endocr J. 55
  
  Pages: 97-103
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 性分化異常症の管理に関する合意見解、日本小児内分泌学会性分化委員会報告2008
- Author(s)
  緒方勤、堀川玲子、長谷川奉延、位田忍、向井徳男、安達昌功、有坂治、藤枝憲二
- Journal Title
  
  日本小児科学会雑誌 112
  
  Pages: 565-578
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Four Japanese patients with adrenal hypoplasia congenitaand hypogonadotropic hypogonadism caused by DAX-1 gene mutations : mutant DAX-1 failed to repress steroidogenicacute regulatory protein (StAR) and luteinizing hormonebeta-subunit gene promoter activity2008
- Author(s)
  Okuhara K, Abe S, Kondo T, Fujita K, Koda N, Mochizuki H, Fujieda K, Talima T
- Journal Title
  
  Endocr J 55
  
  Pages: 97-103
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 性分化異常症の管理に関する合意見解2008
- Author(s)
  緒方勤、堀川玲子、長谷川奉延、位田忍、向井徳男、安達昌功、有坂治、藤枝憲二
- Journal Title
  
  日本小児科学会雑誌 112
  
  Pages: 565-578
- NAID
  10024132484
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations : mutant DAX-1 failed to repress steroidogenic acute regulatory protein (StAR) and luteinizing hormone betasubunit gene nromoter activity2008
- Author(s)
  Okuhara K, Abe S, Kondo T, Fujita K, Koda N, Mochizuki H, Fujieda K, Tajima T
- Journal Title
  
  Endoer J. 55
  
  Pages: 97-103
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations : mutant DAX-1 failed to repress steroidogenic acute regulatory protein(StAR)and luteinizing hormone beta-subunit gene promoter activity2008
- Author(s)
  Okuhara K, Abe S, Kondo T, Fujita K, Koda N, Mochizuki H, Fujieda K, Tajima T
- Journal Title
  
  Endocr J 55
  
  Pages: 97-103
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 性分化異常症の管理に関する合意見解2008
- Author(s)
  緒方勤、堀川玲子、長谷川奉延、位田忍、向井徳男、安達昌功、有坂治、藤枝憲二
- Journal Title
  
  日本小児科学会雑誌 112
  
  Pages: 565-578
- NAID
  10024132484
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations: mutant DAX-1 failed to repress steroidogenic acute regulatory protein(StAR)and luteinizing hormone beta-subunit gene promoter activi2008
- Author(s)
  Okuhara K, Abe S, Kondo T, Fujita K, Koda N, Mochizuki H, Fujieda K, Tajima T
- Journal Title
  
  Endocr J. 55
  
  Pages: 97-103
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Four Japanese patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by DAX-1 gene mutations: mutant DAX-1 failed to repress steroidogenic acute regulatory protein (StAR) and luteinizing hormone beta-subunit gene promoter activity2008
- Author(s)
  Okuhara K, Abe S, Kondo T, Fujita K, Koda N, Mochizuki H, Fujieda K, Tajima T
- Journal Title
  
  Endocr J 55
  
  Pages: 97-103
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 先天性副腎低形成2008
- Author(s)
  藤枝憲二
- Journal Title
  
  日本内科学会誌 97
  
  Pages: 736-742
- NAID
  10021253855
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Fetal growth and IGFs2007
- Author(s)
  Ken Nagaya, Genya Taketazu, Kenji Fujieda
- Journal Title
  
  Clinical Endcrinology 55-4
  
  Pages: 49-55
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591137
[Journal Article] 性分化異常症の診断と治療-特に先天性副腎過形成症を中心に-2007
- Author(s)
  藤枝憲二
- Journal Title
  
  日本小児泌尿器科学会雑誌 16
  
  Pages: 125-129
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Anovel missense mutation(P366T)of the LHX4 gene causes severe combined pituitary hormone deficiency with pituitary hypoplasia, ectopic posterior lobe and a poorly developed sella turcica.2007
- Author(s)
  Tajima T, Hattori T, Nakajima T, Okuhara K, Tsubaki J, Fujieda K
- Journal Title
  
  Endocr J. 54
  
  Pages: 637-641
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 胎児発育とIGF2007
- Author(s)
  長屋建竹田津原野藤枝憲二
- Journal Title
  
  ホルモンと臨床 55
  
  Pages: 49-55
- NAID
  10019499801
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591137
[Journal Article] 胎児発育とIGF2007
- Author(s)
  長屋建, 竹田津原野, 藤枝憲二
- Journal Title
  
  ホルモンと臨床 55
  
  Pages: 49-55
- NAID
  10019499801
- Data Source
  KAKENHI-PROJECT-17591137
[Journal Article] DAX-1異常症2007
- Author(s)
  藤枝憲二
- Journal Title
  
  最新医学 62
  
  Pages: 1241-1247
- NAID
  120001814718
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 性分化異常症の診断と治療-特に先天性副腎過形成症を中心に2007
- Author(s)
  藤枝憲二
- Journal Title
  
  日本小児泌尿器科学会雑誌 16
  
  Pages: 125-129
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] DAX-1異常症2007
- Author(s)
  藤枝憲二
- Journal Title
  
  最新医学 62
  
  Pages: 1241-1247
- NAID
  120001814718
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Consensus statement on management of intersex disorders.2006
- Author(s)
  Hughes IA, Houk C, Ahwed SF, Lee PA, LWPES/ESPE Consensus Group (Fujieda K, et al.
- Journal Title
  
  Arch Dis Child. 91
  
  Pages: 554-563
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 先天性副腎過形成症2006
- Author(s)
  藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ、内分泌症候群(第2版)、別冊日本臨床 No.1
  
  Pages: 673-676
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Global inequalities in paediatric endocrine practice : statement of minimal acceptable care. Statement from the International Societies for Paediatric Endocrinology.2006
- Author(s)
  Savage MO, Cassorla FG, Gluckman PD, Gruters-Kieslich A, Raghupathy P, Silink M, Czernichow P, Chiarelli F, Rogol AD, Crock PA, Cowell CT, Fujieda K, Arnhold IJ
- Journal Title
  
  Horm Res. 65・3
  
  Pages: 111-113
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 20, 22デスモラーゼ欠損症2006
- Author(s)
  藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ No.1、内分泌症候群(第2版)、別冊日本臨床
  
  Pages: 696-698
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] リポイド過形成症2006
- Author(s)
  藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ、内分泌症候群(第2版)、別冊日本臨床 No.1
  
  Pages: 692-695
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Consensus statement on management of intersex disorders2006
- Author(s)
  Hughes IA, Houk C, Ahmed SF, Lee PA, LWPES/ESPE Consensus Group (Fujieda K, et al)
- Journal Title
  
  Arch Dis Child 91
  
  Pages: 554-563
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 先天性副腎過形成症2006
- Author(s)
  藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ No.1、内分泌症候群(第2版)、別冊日本臨床
  
  Pages: 673-676
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Global inequalities in paediatric endocrine practice : statement of minimal acceptable care. Statement from the International Societies for Paediatric Endocrinology.2006
- Author(s)
  Savage MO, Cassorla FG, Gluckman PD, Gruters-Kieslich A, Raghupathy P, Silink M, Czernichow P, Chiarelli F, Rogol AD, Crock PA, Cowell CT, Fujieda K, Arnhold IJ
- Journal Title
  
  Horm Res. 65・3
  
  Pages: 111-113
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome.2006
- Author(s)
  Tajima, T, Nawate M, Takahashi Y, Mizoguchi Y, Sugihara S, Yoshimoto M., Murakami M, Adachi M, Tachibana K., Mochizuki H, Fujieda K
- Journal Title
  
  Endocr J. 53・5
  
  Pages: 647-652
- NAID
  10020613203
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] リポイド過形成症2006
- Author(s)
  藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ No.1、内分泌症候群(第2版)、別冊日本臨床
  
  Pages: 692-695
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Molecular analysis of the CLONKB gene in Japanese patients with classic Bartter syndrome.2006
- Author(s)
  Tajima, T, Nawate M, Takahashi Y, Mizoguchi Y, Sugihara S, Yoshimoto M, Murakami M, Adachi M, Tachibana K, Mochizuki H, Fujieda K
- Journal Title
  
  Endocr J. 53・5
  
  Pages: 647-652
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Consensus statement on management of intersex disorders.2006
- Author(s)
  Hughes IA, Houk C, Ahmed SF, Lee PA, LWPES/ESPE Consensus Group (Fujieda K, et al.
- Journal Title
  
  Arch Dis Child. 91
  
  Pages: 554-563
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] ステロイドサルファターゼ欠損症2006
- Author(s)
  鈴木滋、藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ、内分泌症候群(第2版)、別冊日本臨床 No.3
  
  Pages: 494-496
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 副腎性器症候群2006
- Author(s)
  藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ No.2、内分泌症候群(第2版)、別冊日本臨床
  
  Pages: 643-646
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 20, 22デスモラーゼ欠損症2006
- Author(s)
  藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ、内分泌症候群(第2版)、別冊日本臨床 No.1
  
  Pages: 696-698
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 副腎性器症候群2006
- Author(s)
  藤枝憲二
- Journal Title
  
  新領域別症候群シリーズ、内分泌症候群(第2版)、別冊日本臨床 No.2
  
  Pages: 643-646
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] SCC異常症2006
- Author(s)
  藤枝憲二、勝又規行
- Journal Title
  
  ホルモンと臨床 54
  
  Pages: 61-64
- NAID
  10019247912
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Studies of very severe short stature with severe GH deficiency : From the data registered with the foundation for growth science.2005
- Author(s)
  Hanew K, Tachibana K, Yokoya S, Fujieda K, Tanaka T, Igarashi Y, Shimatsu A, Tanaka H, Tanizawa T, Teramoto A, Nishi Y, Hassegawa Y, Hizuka N, Hirano T, Fujita K
- Journal Title
  
  Endocrine Journal 52(1)
  
  Pages: 37-43
- NAID
  10014483577
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Journal Article] 副腎ステロイド合成酵素異常症の診断基準・病型分類・重症度2005
- Author(s)
  藤枝憲二
- Journal Title
  
  内科 95
  
  Pages: 1835-1839
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Results of long-term follow-up after treatment of central precocious puberty with leuprorelin acetate : evaluation of effectiveness of treatment and recovery of gonadal function. The TAP-144-SR Japanese Study Group on Central Precocious Puberty.2005
- Author(s)
  Tanaka T, Fujieda K, Kugu K, et al.
- Journal Title
  
  J Clin Endocrinol Metab 90・3
  
  Pages: 1371-1376
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 先天性副腎過形成症2005
- Author(s)
  藤枝憲二、向井徳男
- Journal Title
  
  周産期医学 35
  
  Pages: 1245-1248
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Molecular basis of adrenal insufficiency.2005
- Author(s)
  Fujieda K, Tajima T
- Journal Title
  
  Pediatr Res 57
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Molecular basis of adrenal insufficiency2005
- Author(s)
  Fujieda K, Tajima T
- Journal Title
  
  Pediatr Res 57
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Molecular basis of adrenal insufficiency2005
- Author(s)
  Fujieda K, Tajima T
- Journal Title
  
  Pediatr Res 57
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Molecular basis of adrenal insufficiency.2005
- Author(s)
  Fujieda K, Tajima T
- Journal Title
  
  Pediatr Res 57
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Global Inequalities in Paediatric Endocrine Practice : Statement of Minimal Acceptable Care. Statement from the International Societies for Paediatric Endocrinology.2005
- Author(s)
  Savage MO, Fujieda K, Arnhold IJ, et al.
- Journal Title
  
  Horm Res 65・3
  
  Pages: 111-113
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 先天性副腎皮質ステロイド合成異常症の分子基盤2005
- Author(s)
  藤枝憲二、田島敏広、向井徳男
- Journal Title
  
  医学の歩み 213
  
  Pages: 401-407
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 先天性副腎過形成症2005
- Author(s)
  藤枝憲二、向井徳男
- Journal Title
  
  周産期医学 35
  
  Pages: 1245-1248
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] Global Inequalities in Paediatric Endocrine Practice : Statement of Minimal Acceptable Care. Statement from the International Societies for Paediatric Endocrinology.2005
- Author(s)
  Savage MO, Fujieda K, Arnhold IJ, et al.
- Journal Title
  
  Horm Res 65・3
  
  Pages: 111-113
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 副腎ステロイド合成酵素異常症の診断基準・病型分類・重症度2005
- Author(s)
  藤枝憲二
- Journal Title
  
  内科 95
  
  Pages: 1835-1839
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 先天性副腎皮質ステロイド合成異常症の分子基盤2005
- Author(s)
  藤枝憲二、田島敏広、向井徳男
- Journal Title
  
  医学の歩み 213
  
  Pages: 401-407
- Data Source
  KAKENHI-PROJECT-17390294
[Journal Article] 先天性副腎低形成症、小児内分泌・代謝疾患の分子基盤2004
- Author(s)
  向井徳男、藤枝憲二
- Journal Title
  
  小児科診療 67
  
  Pages: 1623-1629
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] An EP4 receptor agonist prevents indomethacin-induced closure of rat ductus arteriosus in vivo.2004
- Author(s)
  Kajino H, Taniguchi T, Fujieda K, Ushikubi F, Muramatsu I.
- Journal Title
  
  Pediatr Res. 56(4)
  
  Pages: 586-590
- NAID
  120003203384
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14570715
[Journal Article] 先天性副腎過形成症、小児内分泌・代謝疾患の分子基盤2004
- Author(s)
  田島敏広、藤枝憲二
- Journal Title
  
  小児科診療 67
  
  Pages: 1617-1622
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 先天性リポイド過形成症及び先天性副腎低形成症の分子病態2004
- Author(s)
  藤枝憲二、向井徳男
- Journal Title
  
  ホルモンと臨床 52冬季増刊号
  
  Pages: 120-125
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] P450 oxidoreductase deficiency: a new disorder of steroidogenesis affecting all microsomal P450 enzymes2004
- Author(s)
  Pandey AV, Fluck CE, Huang N, Tajima T, Fujieda K, Miller WL
- Journal Title
  
  Endocr Res 30
  
  Pages: 881-888
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Studies of very short stature with severe GH deficiency : From the data registered with the foundation for growth science2004
- Author(s)
  Hanew K, Fujieda K, et al.
- Journal Title
  
  Endocrine J 52
  
  Pages: 37-43
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Journal Article] SOX9遺伝子に新規変異を同定したcampomelic dysplasiaの1例2004
- Author(s)
  岡本年男、長屋建、竹田津原野、林時仲、向井徳男、藤枝憲二
- Journal Title
  
  ホルモンと臨床 52増刊
  
  Pages: 140-143
- NAID
  10014248415
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 性腺機能低下症、小児内分泌代謝疾患の分子基盤2004
- Author(s)
  藤枝憲二
- Journal Title
  
  小児科診療 67
  
  Pages: 1651-1659
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 先天性副腎過形成症2004
- Author(s)
  藤枝憲二、向井徳男
- Journal Title
  
  日本臨床 62
  
  Pages: 361-367
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 性を決定するメカニズム2004
- Author(s)
  藤枝憲二
- Journal Title
  
  医学の歩み 208
  
  Pages: 955-961
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome2004
- Author(s)
  Fluck CE, Tajima T, Pandey AV, Arlt W, Okuhara K, Verge CF, Jabs EW, Mendonca BB, Fujieda K, Miller WL
- Journal Title
  
  Nat Genet 36
  
  Pages: 228-230
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] Mutant P450 Oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome.2004
- Author(s)
  Fluck CE, Tajima T, Pandey AV, Arlt W, Okuhara K, Verge CF, Jabs EW, Mendonca BB, Fujieda K, Miller WL
- Journal Title
  
  Nature Genetics 36・3
  
  Pages: 228-230
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] 先天性副腎過形成症の出生前診断・治療2004
- Author(s)
  藤枝憲二
- Journal Title
  
  産婦人科治療 89
  
  Pages: 682-686
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] P450 oxidoreductase deficiency : a new disorder of steroidogenesis affecting all microsomal P450 enzymes.2004
- Author(s)
  Pandey AV, Fluck CE, Huang N, Tajima T, Fujieda K, Miller WL
- Journal Title
  
  Endocrine Research 30・4
  
  Pages: 881-888
- Data Source
  KAKENHI-PROJECT-16086202
[Journal Article] A case of achodroplasia associated with cervicomedullary junction compression2003
- Author(s)
  Takezaki T, Fujieda K et al.
- Journal Title
  
  Clin Pediatr Endocrinol 12
  
  Pages: 39-42
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Journal Article] A case of achondroplasia associated with cervicomedullary-junction compression.2003
- Author(s)
  Takezaki T, Nakai S, Tajima T, Okuhara K, Satoh K, Iwasaki Y, Fujieda K
- Journal Title
  
  Clin Pediatr Endocrinol 12
  
  Pages: 39-42
- NAID
  130004430925
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Journal Article] 内分泌疾患原因遺伝子の解明-成長に関わる遺伝子とその異常2003
- Author(s)
  藤枝憲二
- Journal Title
  
  医学の歩み 206
  
  Pages: 572-578
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Journal Article] A male patient with severe growth retardation, immunodeficiency and diabetes mellitus : A new syndrome2003
- Author(s)
  Ueda O, Fujieda K, et al.
- Journal Title
  
  Clin Pediatr Endocrinol 12(Suppl20)
  
  Pages: 47-49
- NAID
  110002984773
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Journal Article] Sporadic heterozygous frameshift mutation of HESX1 causing pituitqary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient2003
- Author(s)
  Tajima T, Fujieda K, et al.
- Journal Title
  
  J Clin Endocrinol Metab 88
  
  Pages: 45-50
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Journal Article] Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient.2003
- Author(s)
  Tajima T, Hattori T, Nakajima T, Okuhara K, Sato K, Abe S, Nakae J, Fujieda K
- Journal Title
  
  J Clin Endocrinol Metab 88
  
  Pages: 45-50
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Journal Article] A male patient with severe growth retardation, immunodeficiency and diabetes mellitus : a new syndrome?2003
- Author(s)
  Ueda O, Fujine M, Mukai T, Ito Y, Fujieda K
- Journal Title
  
  Clin Pediatr Endocrinol 12(Suppl 20)
  
  Pages: 47-49
- NAID
  110002984773
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15591078
[Presentation] New Bioassay System for GH Determination2009
- Author(s)
  ミレグリマイマイティ, 松尾公美浩, 鈴木滋, 棚橋祐典, 向井徳男, 田島敏広, 藤枝憲二
- Organizer
  日本小児内分泌学会学術集会
- Place of Presentation
  宇都宮
- Year and Date
  2009-10-02
- Data Source
  KAKENHI-PROJECT-21591307
[Presentation] Congenital lipoid adrenal hyperplasia with bilateral ovarian endometrioma2008
- Author(s)
  Sugawara T, Kudo M, Fujieda K, Sakuragi N
- Organizer
  41st Annual Meeting of the Society for the Study of Reproduction
- Place of Presentation
  Kailua-Kona, USA
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Congenital lipoid adrenal hyperplasia with bilateral ovarian endometrioma2008
- Author(s)
  Sugawara T, Kudo M, Fujieda K, Sakuragi N
- Organizer
  41st Annual Meeting of the Society for Study of Reproduction
- Place of Presentation
  Kailua-Kona, USA
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Congenital lipoid adrenal hyperplasia with bilateral ovarian endometrioma2008
- Author(s)
  Sugawara T, Kudo M, Fujieda K, Sakuragi N
- Organizer
  41st Annual Meeting of the Society for the Study of Reproduction
- Place of Presentation
  Kailua-Kona, USA
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] NR5A1遺伝子異常(Ad4/BP)による精巣形成不全の1例2007
- Author(s)
  田島敏広、石津桂、藤枝憲二
- Organizer
  第15回日本ステロイドホルモン学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2007-11-24
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] 性分化異常症の診断と治療-特に先天性副腎過形成症を中心に-2007
- Author(s)
  藤枝憲二
- Organizer
  第16回日本小児泌尿器科学会総会
- Place of Presentation
  神戸
- Year and Date
  2007-07-14
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Disorders of steroidogenesis, other than 21-hydroxylase2007
- Author(s)
  Fujieda K
- Organizer
  ENDO 2007 Meet-the-Professor Session
- Place of Presentation
  Toronto, Canada
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] NR5A1遺伝子異常(Ad4/BP)による精巣形成不全の1例2007
- Author(s)
  田島敏広、石津桂、藤枝憲二
- Organizer
  第15回日本ステロイドホルモン学会学術集会
- Place of Presentation
  仙台市
- Year and Date
  2007-11-24
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] NR5A1 遺伝子異常(Ad4/BP)による精巣形成不全の1 例2007
- Author(s)
  田島敏広、石津桂、藤枝憲二
- Organizer
  第15回日本ステロイドホルモン学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2007-11-24
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] 性分化異常症の診断と治療-特に先天性副腎過形成症を中心に-2007
- Author(s)
  藤枝憲二
- Organizer
  第16回日本小児泌尿器科学会総会
- Place of Presentation
  神戸
- Year and Date
  2007-07-14
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Steroidogenic acute regulatory protein-binding protein is associated with apoptosis and controls steroidogenesis2007
- Author(s)
  Sugawara T, Hoshi N, Fujieda K
- Organizer
  ENDO 2007
- Place of Presentation
  Toronto, Canada
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Disorders of steroidogenesis, other than 21-hydroxylase2007
- Author(s)
  Fujieda K
- Organizer
  ENDO 2007 Meet-the-Professor Session
- Place of Presentation
  Toronto, Canada
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Steroidogenic acute regulatory protein-binding protein is associated with apoptosis and controls steroidogenesis2007
- Author(s)
  Sugawara T, Hoshi N, Fujieda K
- Organizer
  ENDO 2007
- Place of Presentation
  Toronto, Canada
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] P450 oxidoreductase(POR)欠損症の遺伝子診断2007
- Author(s)
  田島敏広、藤枝憲二
- Organizer
  第17回臨床内分泌Update
- Place of Presentation
  東京
- Year and Date
  2007-03-10
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] NR5A1遺伝子異常(Ad4/BP)による精巣形成不全の1例2007
- Author(s)
  田島敏広、石津桂、藤枝憲二
- Organizer
  第15回日本ステロイドホルモン学会学術集会
- Place of Presentation
  仙台市
- Year and Date
  2007-11-24
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] P450 oxidoreductase(POR)欠損症の遺伝子診断2007
- Author(s)
  田島敏広、藤枝憲二
- Organizer
  第17回臨床内分泌Update
- Place of Presentation
  東京
- Year and Date
  2007-03-10
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] International newborn screening(NBS)collaborative study on 21-hydroxylase deficiency congenital adrenal hyperplasia(CAH)2006
- Author(s)
  Fujieda K, Pang S
- Organizer
  Workshop 5, 6th Meeting of the International Society for Neonatal Screening
- Place of Presentation
  Awaji, Japan
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] The genetic mutations of adrenal insufficiency2006
- Author(s)
  Fujieda K, Tajima T, Mukai T
- Organizer
  Symposium IV, Adrenal, 4th Biennial Scientific Meeting Asia Pacific Paediatric Endocrine Society 2006
- Place of Presentation
  Pattaya, Thailand
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] New disease in CAH screening2006
- Author(s)
  Tajima T, Fujieda K
- Organizer
  Workshop 5, 6th Meeting of the International Society for Neonatal Screening
- Place of Presentation
  Awaji, Japan
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Congenital adrenal disorders : From newborn screening to molecular mechanism2006
- Author(s)
  Fujieda K
- Organizer
  LWPES Trans-Pacific Lecture, Pediatric Academic Societies' 2006 Annual Meeting
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] The impact of IGFs polymorphisms in feto-placental growth.2006
- Author(s)
  Ken Nagaya, Genya Taketazu, Kenji Fujieda.
- Organizer
  The 40^<th> Annual Meeting of Japanese Society for Pediatric Endocrinology
- Place of Presentation
  Hamamatsu
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591137
[Presentation] Disorders of steroidogenesis, other than 21-hydroxylase2006
- Author(s)
  Fujieda K
- Organizer
  ENDO 2006 Meet-the-Professor Session
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] 先天性副腎疾患Update2006
- Author(s)
  藤枝憲二
- Organizer
  第9回日本内分泌学会学術総会教育講演
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Congenital adrenal disorders: From newborn screening to molecular mechanism2006
- Author(s)
  Fujieda K
- Organizer
  LWPES Trans-Pacific Lecture, Pediatric Academic Societies'2006 Annual Meeting
- Place of Presentation
  San Francisco, USA
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] New disease in CAH screening2006
- Author(s)
  Tajima T, Fujieda K
- Organizer
  Workshop 5, 6th Meeting of the International Society for Neonatal Screening
- Place of Presentation
  Awaji, Japan
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Association of spermatogenesis with Ser164Arg and Arg417Trp polymorphism in the gene of steroidogenic acute regulatory protein-binding protein2006
- Author(s)
  Sugawara T, Makita Y, Fujieda K
- Organizer
  ENDO 2006
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Polymorphism in paternal allele of IGF-2 gene associate with fetal and placental growth in Japanese.2006
- Author(s)
  Ken Nagaya, Genya Taketazu, Kenji Fujieda.
- Organizer
  The 3^<rd> International Congress Of the GRS and the IGF Society
- Place of Presentation
  Kobe
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591137
[Presentation] National survey of the treatment for congenital adrenal hyperplasia detected by mass-screening2006
- Author(s)
  Adachi M, Fujieda K
- Organizer
  Workshop 5, 6th Meeting of the International Society for Neonatal Screening
- Place of Presentation
  Workshop 5, 6th Meeting of the International Society for Neonatal Screening
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Disorders of steroidogenesis, other than 21-hydroxylase2006
- Author(s)
  Fujieda K
- Organizer
  ENDO 2006 Meet-the-Professor Session
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Association of spermatogenesis with Ser164Arg and Arg417Trp polymorphism in the gene of steroidogenic acute regulatory protein-binding protein2006
- Author(s)
  Sugawara T, Makita Y, Fujieda K
- Organizer
  ENDO 2006
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] 性分化異常症の診断と治療-特に先天性副腎過形成症を中心に2006
- Author(s)
  藤枝憲二
- Organizer
  シンポジウム5「小児泌尿器科:半陰陽の診断と治療」、第94回日本泌尿器科学総会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] International newborn screening (NBS) collaborative study on 21-hydroxylase deficiency congenital adrenal hyperplasia (CAH)2006
- Author(s)
  Fujieda K, Pang S
- Organizer
  Workshop 5, 6th Meeting of the International Society for Neonatal Screening
- Place of Presentation
  Awaji, Japan
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Fetal grwth and IGFs.2006
- Author(s)
  Ken Nagaya, Genya Taketazu, Kenji Fujieda.
- Organizer
  The 3^<rd> International Congress Of the GRS and the IGF Society
- Place of Presentation
  Kobe
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591137
[Presentation] 先天性副腎疾患Update2006
- Author(s)
  藤枝憲二
- Organizer
  第9回日本内分泌学会学術総会教育講演
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] The impact of IGFs polymorphisms in feto-placental growth.2006
- Author(s)
  Ken Nagaya, Genya Taketazu, Kenji Fujieda.
- Organizer
  The 10^<th> Pediatric Study Ggroup of Molecular Endocrinology
- Place of Presentation
  Kitahiroshima
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591137
[Presentation] 性分化異常症の診断と治療-特に先天性副腎過形成症を中心に、シンポジウム5「小児泌尿器科 : 半陰陽の診断と治療2006
- Author(s)
  藤枝憲二
- Organizer
  第94回日本泌尿器科学総会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] The genetic mutations of adrenal insufficiency2006
- Author(s)
  Fujieda K, Tajima T, Mukai T
- Organizer
  Symposium IV, Adrenal, 4th Biennial Scientific Meeting Asia Pacific Paediatric Endocrine Society 2006
- Place of Presentation
  Pattaya, Thailand
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] P450と内分泌疾患-先天性副腎皮質過形成症を中心に2005
- Author(s)
  田島敏広、藤枝憲二
- Organizer
  第15回臨床内分泌代謝Update
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Two Japanese patients caused by P450 oxidoreductase(POR)deficiency2005
- Author(s)
  Tajima T, Tsubaki J, Okuhara K, Ogawa E, Fujieda K
- Organizer
  ESPE/LWPES 7th Joint Meeting
- Place of Presentation
  Lyon, France
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] ヒト副腎・生殖腺の発生分化・機能の異常による性分化異常症2005
- Author(s)
  藤枝憲二
- Organizer
  第10回日本生殖内分泌学会シンポジウム「性分化異常の基礎と臨床」
- Place of Presentation
  東京
- Year and Date
  2005-11-03
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Transcription factors and adrenal development2005
- Author(s)
  Fujieda K, Mukai T, Okuhara K, Tajima T
- Organizer
  ESPE/LWPES 7th Joint Meeting
- Place of Presentation
  Lyon, France
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] シンポジウム「性成熟異常症の最近の進歩」AHC(DAX-1)異常症2005
- Author(s)
  向井徳男、藤枝憲二
- Organizer
  第78回日本内分泌学会学術総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] ヒト副腎・生殖腺の発生分化機能の異常による性分化異常症2005
- Author(s)
  藤枝憲二
- Organizer
  第10回日本生殖内分泌学会シンポジウム「性分異常の基礎と臨床」
- Place of Presentation
  東京
- Year and Date
  2005-11-03
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] アンドロゲン受容体遺伝子に新規部分欠失を同定したアンドロゲン不応症の同胞例2005
- Author(s)
  向井徳男、鈴木滋、松尾公美浩、上田修、安達かおり、藤枝憲二
- Organizer
  第39回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] 先天性副腎過形成症の遺伝子診断と出生前診断・治療2005
- Author(s)
  田島敏広、藤枝憲二
- Organizer
  第108回日本小児科学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] アンドロゲン受容体遺伝子に新規部分欠失を同定したアンドロゲン不応症の同胞例2005
- Author(s)
  向井徳男、鈴木滋、松尾公美浩、上田修、安達かおり、藤枝憲二
- Organizer
  第39回日本小児内分泌学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] シンポジウム「性成熟異常症の最近の進歩」AHC (DAX-1)異常症2005
- Author(s)
  向井徳男、藤枝憲二
- Organizer
  第78回日本内分泌学会学術総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Two novel mutations in SOX9 gene in the patients with campomelic dysplasia2005
- Author(s)
  Mukai T, Okamoto T, Suzuki S, Matsuo K, Ueda O, Ito Y, Fujieda K
- Organizer
  ESPE/LWPES 7th Joint Meeting
- Place of Presentation
  Lyon, France
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Transcription factors and adrenal development2005
- Author(s)
  Fujieda K, Mukai T, Okuhara K, Tajima T
- Organizer
  ESPE/LWPES 7th Joint Meeting
- Place of Presentation
  Lyon, France
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] 新生児マススクリーニングでみつかる副腎疾患2005
- Author(s)
  田島敏広、藤枝憲二
- Organizer
  第33回新生児マススクリーニング学会
- Place of Presentation
  久留米
- Year and Date
  2005-10-07
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Two novel mutations in SOX9 gene in the patients with campomelic dysplasia2005
- Author(s)
  Mukai T, Okamoto T, Suzuki S, Matsuo K, Ueda O, Ito Y, Fujieda K
- Organizer
  ESPE/LWPES 7th Joint Meeting
- Place of Presentation
  Lyon, France
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Two Japanese patients caused by P450 oxidoreductase (POR) deficiency2005
- Author(s)
  Tajima T, Tsubaki J, Okuhara K, Ogawa E, Fujieda K
- Organizer
  ESPE/LWPES 7th Joint Meeting
- Place of Presentation
  Lyon, France
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] 先天性副腎過形成症の遺伝子診断と出生前診断・治療2005
- Author(s)
  田島敏広、藤枝憲二
- Organizer
  第108回日本小児科学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] P450と内分泌疾患-先天性副腎皮質過形成症を中心に2005
- Author(s)
  田島敏広、藤枝憲二
- Organizer
  第15回臨床内分泌代謝Update
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-17390294
[Presentation] Molecular genetics on adrenal insufficiency2004
- Author(s)
  Fujieda K
- Organizer
  5th Asia Pacific Regional Meeting of International Society for Neonatal Screening
- Place of Presentation
  Shanghai, China
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] 先天性副腎過形成症-スクリーニング、出生前診断・治療、分子遺伝学2004
- Author(s)
  藤枝憲二
- Organizer
  日本マススクリーニング学会ランチョンセミナー
- Place of Presentation
  仙台
- Year and Date
  2004-10-09
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] オーバービュー、先天性副腎皮質ステロイド合成異常症の臨床2004
- Author(s)
  藤枝憲二
- Organizer
  クリニカルアワー、第77回日本内分泌学会学術総会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] 副腎不全の分子基盤2004
- Author(s)
  藤枝憲二
- Organizer
  日本小児内分泌学会ランチョンセミナー
- Place of Presentation
  神戸
- Year and Date
  2004-09-23
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] Microsomal-P450 oxidoreductase遺伝子異常によって発症したCYP21, CYP17複合欠損症2004
- Author(s)
  田島敏広、奥原宏治、椿淳子、藤枝憲二
- Organizer
  第77回日本内分泌学会学術総会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-16086202
[Presentation] campomelic dysplasia 3症例におけるSOX9遺伝子の解析2004
- Author(s)
  向井徳男、岡本年男、石井玲、鈴木滋、松尾公美浩、藤根美穂、上田修、伊藤善也、藤枝憲二
- Organizer
  第38回日本小児内分泌学会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-16086202

1. NAGAYA Ken (80396382)

# of Collaborated Projects: 4 results

# of Collaborated Products: 8 results
2. MATSUURA Nobuo (50002332)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
3. NAKAE Jun (00344573)

# of Collaborated Projects: 3 results

# of Collaborated Products: 1 results
4. HAYASHI Tokitugi (40322911)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. MUKAI Tokuo (50374799)

# of Collaborated Projects: 2 results

# of Collaborated Products: 26 results
6. TAJIMA Toshihiro (50333597)

# of Collaborated Projects: 2 results

# of Collaborated Products: 27 results
7. SUGAWARA Teruo (40250451)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
8. MAKITA Yoshio (20271778)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
9. HONMA Kenichi (40113625)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
10. SAITOH Shinji (00281824)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
11. YOSHIDA Makoto (20333700)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
12. NAKAMURA Eiki (20396352)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
13. SUZUKI Shigeru (80516394)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
14. KAJII Naofumi (20194730)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. TAGAWA Yoshitsugu (40109426)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. MOROHASHI Kenichirou (30183114)

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17. HOSHI Nobuhiko (10209223)

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18. SAKURAGI Noriaki (70153963)

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19. KISHI Reiko (80112449)

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20. NAKAZAWA Hiroyuki (50150173)

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21. FUJITA Shouichi (10143314)

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22. SATA Fumihiro (90187154)

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23. KAJINO Hiroki (70292109)

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24. TSUDA Naoya (10302001)

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25. 松尾公美浩 (40548707)

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26. 小柳知彦 (80001923)

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27. 藤本征一郎 (60001898)

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28. 竹田津原野 (10360992)

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# of Collaborated Products: 2 results
29. FUJITA Kouzou

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FUJIEDA Kenji 藤枝 憲二

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候補遺伝子解析並びにハプロタイプ解析による成長障害の成因の同定Principal Investigator

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Comprehensive investigation of etiology and pathophysiology of disorders of sex development(DSD)Principal Investigator

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Search for the novel etiology in disorders of sex development (DSD) caused by abnormalities of adrenal glands and gonads.Principal Investigator

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Analysis of molecular mechanism of GH effect on life spanPrincipal Investigator

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リポイド過形成症の病因としてのコレステロール側鎖切断酵素遺伝子異常の検索Principal Investigator

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機能獲得型カルシウムセンサー受容体異常に関する分子遺伝学的研究Principal Investigator

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STRUCTURE-FUNCTION ANALYSIS OF DAX-1 USING Molecular analysisPrincipal Investigator

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FUJIEDA Kenji 藤枝憲二