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

Tajima Toshihiro  田島 敏広

ORCIDConnect your ORCID iD *help
… Alternative Names

TAJIMA Toshihiro  田島 敏広

Less
Researcher Number 50333597
Other IDs
External Links
Affiliation (Current) 2025: 自治医科大学, 医学部, 教授
Affiliation (based on the past Project Information) *help 2013 – 2015: 北海道大学, 医学(系)研究科(研究院), 講師
2012: 北海道大学, 医学研究科, 講師
2010: 北海道大学, 医学研究科, 講師
2008 – 2010: Hokkaido University, 大学院・医学研究科, 講師
2007: 北海道大学, 大学院・医学系・研究科, 講師 … More
2006: 北海道大学, 医学研究科, 講師
2006: 北海道大学, 大学院・医学系研究科, 講師
2006: Hokkaido Uni., Grad.School of Med., Lec., 大学院医学研究科, 講師
2005: 北海道大学, 大学院・医学系研究科, 助手
2002 – 2005: 北海道大学, 大学院・医学研究科, 助手 Less
Review Section/Research Field
Principal Investigator
Pediatrics / Pediatrics / Endocrinology
Except Principal Investigator
Pediatrics / Biological Sciences
Keywords
Principal Investigator
下垂体 / NR5A1 / Bartter syndrome / Mineralocorticoid / Gonad / Adrenal / 再生 / 過形成 / ミネラルコルチコイド / NR5Al … More / 性腺 / 副腎皮質 / バーター症候群 / 副腎 / P450オキシドレダクターゼ / Pituitary / Hypothalamus / Adenovirus vector / Gene therapy / CAH / ACTH / 21水酸化酵素 / 視床下部 / アデノウイルスベクター / 遺伝子治療 / 先天性副腎過形成 / TSH / 甲状腺機能低下症 / 変異 / TGFB / POU1F1 / 肥満 / 中枢性甲状線機能低下症 / IGSF1 / マススクリーニング / 甲状腺 / 転写因子 / 無眼球症 / クロマチンリモデリン / 中枢性性腺機能低下症 / 複合型下垂体前葉ホルモン欠損 / OTX2 / GLI2 / Septo-optic dysplasai / 中枢性性腺機能低 / CHD7 / 発生 / 小児内分泌学 … More
Except Principal Investigator
発光レポーター測定 / 概日リズム / GnRH遺伝子 / 思春期発来 / Kisspeptin / 時計遺伝子 / 思春期発来メカニズム / 生物時計 / 小児内分泌学 / Yeast Two-hybrid Screening / 外陰部異常 / 複合型ステロイド合成障害 / SOX9 / アンドロゲン受容体 / WT1 / 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 / yeast two-hybrid screening / アンドロゲン不応症 / Ad4BP-SF-1 / 副腎低形成症 / DAX-1 / リポイド過形成症 / yeast two-hbrid screening / StAR / POR異常症 / Antley-Bixler症候群 / 相互作用因子 / 先天性副腎低形成症 / 先天性副腎過形成症 / 性分化異常症 (DSD) Less
  • Research Projects

    (6 results)
  • Research Products

    (128 results)
  • Co-Researchers

    (9 People)
  •  The mechanism of congenital central hypothyroidism caused by IGSF1 deficiencyPrincipal Investigator

    • Principal Investigator
      Tajima Toshihiro
    • Project Period (FY)
      2013 – 2015
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Endocrinology
    • Research Institution
      Hokkaido University
  •  Functional and chronobiological analysis of factors for the timing of puberty in GnRH neurons

    • Principal Investigator
      TANAHASHI Yusuke
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Asahikawa Medical College
  •  Molecular basis of congenital pituitary defectPrincipal Investigator

    • Principal Investigator
      TAJIMA Toshihiro
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Hokkaido University
  •  Analysis of Mechanism of Adrenal RegenerationPrincipal Investigator

    • Principal Investigator
      TAJIMA Toshihiro
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Hokkaido University
  •  Search for the novel etiology in disorders of sex development (DSD) caused by abnormalities of adrenal glands and gonads.

    • 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
  •  Analysis of gene therapy and its effect to hypothalamic-pituitary-adrenal axisPrincipal Investigator

    • Principal Investigator
      TAJIMA Toshihiro
    • Project Period (FY)
      2002 – 2003
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      HOKKAIDO UNIVERSITY

All 2016 2015 2014 2013 2011 2010 2009 2008 2007 2006 2005 2004 Other

All Journal Article Presentation Book

  • [Book] 中山書店2014

    • Author(s)
      田島敏広
    • Total Pages
      235
    • Publisher
      ビギナーのための小児内分泌診療ガイド
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Book] 成長障害のマネージメント2013

    • Author(s)
      田島敏広
    • Total Pages
      211
    • Publisher
      医薬ジャーナル
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Book] ワンランク上の小児の臨床検査2013

    • Author(s)
      田島敏広
    • Total Pages
      549
    • Publisher
      総合医学社
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Book] 急性副腎不全 今日の治療指針2006

    • Author(s)
      田島 敏広
    • Total Pages
      195
    • Publisher
      医学書院、東京
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [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
  • [Journal Article] Neonatal mass screening for 21-hydroxylase deficiency2016

    • Author(s)
      Tajima T, Fukushi M.
    • Journal Title

      Clinical Pediatric Endocrinology

      Volume: 25 Issue: 1 Pages: 1-8

    • DOI

      10.1297/cpe.25.1

    • NAID

      130005122126

    • ISSN
      0918-5739, 1347-7358
    • Language
      English
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan2015

    • Author(s)
      Tanaka T, Igarashi Y, Ozono K, Ohyama K, Ogawa M, Osada H, Onigata K, Kanzaki S, Kohno H, Seino Y, Takahashi H, Tajima T, Tachibana K, Tanaka H, Nishi Y, Hasegawa T, Fujita K, Yorifuji T, Horikawa R, Yokoya S.
    • Journal Title

      Clinical Pediatric Endocrinology

      Volume: 24 Issue: 4 Pages: 167-173

    • DOI

      10.1297/cpe.24.167

    • NAID

      130005104366

    • ISSN
      0918-5739, 1347-7358
    • Language
      English
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of <i>NR3C2</i>2015

    • Author(s)
      Morikawa S, Komatsu N, Sakata S, Nakamura-Utsunomiya A, Okada S, Tajima T.
    • Journal Title

      Clinical Pediatric Endocrinology

      Volume: 24 Issue: 3 Pages: 135-138

    • DOI

      10.1297/cpe.24.135

    • NAID

      130005088094

    • ISSN
      0918-5739, 1347-7358
    • Language
      English
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)2015

    • Author(s)
      Nagasaki K, Ishi T, Anzo M, Adaci M, Onigata K, Kusua S, Harada S, HOrikawa R, Minagawa M, MInamitanu K, Yamakami Y, Fukushi M, Tajima T.
    • Journal Title

      Clin Pediatr Endocrinol

      Volume: 18 Pages: 78-98

    • NAID

      130005088095

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] A Japanese family with nonautoimmune hyperthyroidism caused by a novel heterozygous thyrotropin receptor gene mutation.2014

    • Author(s)
      Nakamura A, Morikawa S, Aoyagi H, Ishizu K, Tajima T.
    • Journal Title

      Pediatr Res

      Volume: 75 Issue: 6 Pages: 749-753

    • DOI

      10.1038/pr.2014.34

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Results from 28 years of newborn screening for congenital adrenal hyperplasia in sapporo.2014

    • Author(s)
      Morikawa S, Nakamura A, Fujikura K, Fukushi M, Hotsubo T, Miyata J, Ishizu K, Tajima T.
    • Journal Title

      Clin Pediatr Endocrinol.

      Volume: 23 Pages: 35-43

    • NAID

      130004853601

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642H/R642W Mutation in the SLC12A3 Gene.2014

    • Author(s)
      Makino S, Tajima T, Shinozuka J, Ikumi A, Awaguni H, Tanaka S, Maruyama R, Imashuku S.
    • Journal Title

      Case Rep Pediatr.

      Volume: 2014 Pages: 56-56

    • DOI

      10.1155/2014/279389

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Two heterozygous mutations of the AMH gene in a Japanese patient with persistent Müllerian duct syndrome.2014

    • Author(s)
      Morikawa S, Moriya K, Ishizu K, Tajima T.
    • Journal Title

      J Pediatr Endocrinol Metab.

      Volume: 27 Pages: 1223-1226

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Prognosis of primary aldosteronism in Japan: results from a nationwide epidemiological study.2014

    • Author(s)
      Miyake Y, Tanaka K, Nishikawa T, Naruse M, Takayanagi R, Sasano H, Takeda Y, Shibata H, Sone M, Satoh F, Yamada M, Ueshiba H, Katabami T, Iwasaki Y, Tanaka H, Tanahashi Y, Suzuki S, Hasegawa T, Katsumata N, Tajima T, Yanase T.
    • Journal Title

      Endocrine Journal

      Volume: 61 Pages: 35-40

    • NAID

      130004443933

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Neonatal screening and a new cause of congenital central hypothyroidism.2014

    • Author(s)
      Tajima T, Nakamura A, Morikawa S, Ishizu K.
    • Journal Title

      Ann Pediatr Endocrinol Metab.

      Volume: 19 Issue: 3 Pages: 117-121

    • DOI

      10.6065/apem.2014.19.3.117

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] 先天性中枢性甲状腺機能低下症の新たな病態―Immunoglobulin superfamily member 1遺伝子異常症―2014

    • Author(s)
      田島敏広
    • Journal Title

      日児誌

      Volume: 118 Pages: 1578-1587

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Polyarthritis caused by methimazole in two Japanese patients with graves' disease.2013

    • Author(s)
      Nihei H, Tada H, Naruse Y, Izawa M, Kato M, Okuno H, Nakamura A, Ishizu K, Hamajima T, Tajima T.
    • Journal Title

      Journal of Clinnical Research Pediatric Endocrinology

      Volume: 5 Issue: 4 Pages: 270-272

    • DOI

      10.4274/jcrpe.1055

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Molecular and Clinical Findings in Patients with LHX4 and OTX2 Mutations.2013

    • Author(s)
      Tajima T, Ishizu K, Nakamura A.
    • Journal Title

      Clinical Pedaitric Endocrinology

      Volume: 22 Pages: 15-23

    • NAID

      10031199648

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] A novel mutation of IGSF1 in a Japanese patient of congenital central hypothyroidism without macroorchidism.2013

    • Author(s)
      Tajima T, Nakamura A, Ishizu K
    • Journal Title

      Endocrine Journal

      Volume: 60 Pages: 29-34

    • NAID

      10031156748

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Three novel IGSF1 mutations in four Japanese patients with X-linked congenital central hypothyroidism.2013

    • Author(s)
      Nakamura A, Bak B, Silander TL, Lam J, Hotsubo T, Yorifuji T, Ishizu K, Bernard DJ, Tajima T.
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism

      Volume: 98 Issue: 10 Pages: E1682-E1691

    • DOI

      10.1210/jc.2013-1224

    • NAID

      120005537445

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Journal Article] Congenital hypothyroidism caused by a PAX8 gene mutation manifested as sodium/iodide symporter gene defect.2011

    • Author(s)
      Jo W, Ishizu K, Fujieda K, Tajima T
    • Journal Title

      Journal of Thyroid Research

      Volume: On-line Pages: 12-16

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] A novel PAX4 mutation in a Japanese patient with maturity onset diabetes of the young (MODY)2011

    • Author(s)
      Jo W, Endo M, Nakamura A, Ishidu K, Tajima T.
    • Journal Title

      Tohoku Journal of Experimental Medicine

      Volume: VOL.223 Pages: 113-118

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Identification and functional analysis of novel calcium-sensing receptor gene mutation in familial hypocalciuric hypercalcemia.2010

    • Author(s)
      Nanjo K, Nagai S, Shimizu C, Tajima T, Kondo T, Miyoshi H, Yoshioka N, Koike T.
    • Journal Title

      Endocrine Journal

      Volume: VOL.57 Pages: 782-792

    • NAID

      10029586221

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome.2010

    • Author(s)
      Nakamura A, Fujiwara F, Hasegawa Y, Ishizu K, Mabe A, Nakagawa H, Nagasaki K, Jo W, Tajima T
    • Journal Title

      Endocr J.[Epub ahead of print]

    • NAID

      10029587711

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Heterozygous orthodenticle homeobox 2 mutations are associated with variable pituitary phenotype.2010

    • Author(s)
      Dateki S, Kosaka K, Hasegawa K, Tanaka H, Azuma N, Yokoya S, Muroya K, Adachi M, Tajima T, Motomura K, Kinoshita E, Moriuchi H, Sato N, Fukami M, Ogata T.
    • Journal Title

      J Clin Endocrinol Metab 95

      Pages: 756-764

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism.2010

    • Author(s)
      Adachi M, Asakura Y, Muroya K, Tajima T, Fujieda K, Kuribayashi E, Uchida S.
    • Journal Title

      Clinical and Experimental Nephrology

      Volume: VOL.14 Pages: 228-232

    • NAID

      10027706204

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Problems in diagnosing atypical Gitelman's syndrome presenting with normomagnesaemia.2010

    • Author(s)
      Nakamura A, Shimizu C, Nagai S, Yoshida M, Aoki K, Kondo T, Miyoshi H, Wada N, Tajima T, Terauchi Y, Yoshioka N, Koike T
    • Journal Title

      Clin Endocrinol 72

      Pages: 272-276

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] 先天性副腎過形成の成因と治療の最近の話題2010

    • Author(s)
      田島敏広、中村明枝、城和歌子、石津桂、奥原宏治、藤枝憲二
    • Journal Title

      日本小児科学会雑誌 114

      Pages: 1373-1380

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] 成長ホルモン分泌不全性低身長 小児の薬の使い方2010

    • Author(s)
      田島敏広
    • Journal Title

      小児内科増刊号 42

      Pages: 565-666

    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Loss of function mutation (V101A) in a LIM domain of the LHX4 gene causes combined pituitary hormone deficiency.2010

    • Author(s)
      Tajima T, Ishizu K, Yorifuji T.
    • Journal Title

      Exp Clin Endocrinol Diabetes 118

      Pages: 405-409

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism.2010

    • Author(s)
      Adachi M, Asakura Y, Muroya K, Tajima T, Fujieda K, Kuribayashi E, Uchida S
    • Journal Title

      Clin Exp Nephrol 14

      Pages: 228-232

    • NAID

      10027706204

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome.2010

    • Author(s)
      Nakamura A, Fujiwara F, Hasegawa Y, Ishizu K, Mabe A, Nakagawa H, Nagasaki K, Jo W, Tajima T.
    • Journal Title

      Endocrine Journal

      Volume: 58 Pages: 123-130

    • NAID

      10029587711

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Cytochrome P450 Oxidoreductase Deficiency : Identification and Characterization of Biallelic Mutations and GenotypePhenotype 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. Fuiieda K. Oeata 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 (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 46, XY disorders of sex development(DSD)patient without adrenal failure.2009

    • Author(s)
      Tajima T, et al.
    • Journal Title

      Endocrine Journal 56

      Pages: 619-624

    • NAID

      10026914347

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Results of neonates with elevated free thyroxine levels detected by a neonatal screening system.2009

    • Author(s)
      Tajima T, Jo W, Fujikura K, Fukushi M, Fujieda K
    • Journal Title

      Pediatr Res 66

      Pages: 312-316

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] A Novel Mutation(V101A) of the LHX4 Gene in a Japanese Patient with Combined Pituitary Hormone Deficiency.2009

    • Author(s)
      Tajima T, et al.
    • Journal Title

      Experimental and Clinical Endocrinology and Met abolism (e-pub)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] OTX2 loss of function mutation causes anophthalmia and combined pituitary hormone deficiency with a small anterior and ectopic posterior pituitary.2009

    • Author(s)
      Tajima T, Ohtake A, Hoshino M, Amemiya S, Sasaki N, Ishizu K, Fujieda K
    • Journal Title

      J Clin Endocrinol Metab. 94

      Pages: 314-319

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] 先天性複合型下垂体機能低下症2009

    • Author(s)
      田島敏広
    • Journal Title

      ゲノム医学 9

      Pages: 55-59

    • Data Source
      KAKENHI-PROJECT-20591213
  • [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] OTX2 loss of function mutation causes anophthalmia and combined pituitary hormone deficiency with a small anterior and ectopic posterior pituitary2009

    • Author(s)
      Tajima T, et al
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 94

      Pages: 314-319

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Elevated free thyroxine levels detected by a neonatal screening system.2009

    • Author(s)
      Tajima T, et al.
    • Journal Title

      Pediatric Research 66

      Pages: 312-316

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article]2009

    • Author(s)
      田島敏広
    • Journal Title

      小児内分泌学(診断と治療社)

      Pages: 178-183

    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Prenatal diagnosis and treatment of steroid 21-hydroxylase deficiency.2008

    • Author(s)
      田島敏広, 藤枝憲二
    • Journal Title

      Clin Pediatr Endocrinol. 17

      Pages: 95-102

    • NAID

      10031199581

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] Case study of a 15-year-old boy with McCune-Albright syndrome combined with pituitary gigantism : effect of octreotide-long acting release (LAR) and cabergoline therapy.2008

    • Author(s)
      Tajima T, Tsubaki J, Ishizu K, Jo W, Ishi N, Fujieda K
    • Journal Title

      Endocr J. 55

      Pages: 595-599

    • NAID

      10021266702

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Journal Article] 複合型下垂体機能不全小児疾患診療のための病態生理2008

    • Author(s)
      田島敏広
    • Journal Title

      小児内科 40

      Pages: 661-666

    • Data Source
      KAKENHI-PROJECT-20591213
  • [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-20591213
  • [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] 複合型下垂体機能不全 小児疾患診療のための病態生理2008

    • Author(s)
      田島敏広
    • Journal Title

      小児内科 40

      Pages: 661-666

    • Data Source
      KAKENHI-PROJECT-20591213
  • [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] 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] Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome2006

    • Author(s)
      Tajima T, et al.
    • Journal Title

      Endocrine Journal 53

      Pages: 647-652

    • NAID

      10020613203

    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Two patients with Gitelman syndrome.2006

    • Author(s)
      TOSHIHIRO TAJIMA
    • Journal Title

      Clinical Pediatric Endocrinology 15

      Pages: 137-142

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency : Implication for the backdoor pathway to dihydrotestosterone.2006

    • Author(s)
      Homma K, Tajima T., et al.
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 91

      Pages: 2643-2649

    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Molecular genetic analysis of MODY candidate genes in Japanese patients with non-obese juvenile onset diabetes mellitus.2006

    • Author(s)
      Kagami-Takasugi, M, Tajima T et al.
    • Journal Title

      Journal of Pediatric Endocrinology and Metabolism 19

      Pages: 143-148

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Two patients with Gitelman syndrome.2006

    • Author(s)
      Tajima T et al.
    • Journal Title

      Clinical Pediatric Endocrinology 15

      Pages: 137-142

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [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] Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome2006

    • Author(s)
      TOHSIHIRO TAJIMA
    • Journal Title

      Endocrine Journal 53

      Pages: 647-652

    • NAID

      10020613203

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Molecular genetic analysis of MODY candidate genes in Japanese patients with non-obese juvenile onset diabetes mellitus.2006

    • Author(s)
      Kagami-Takasugi, M, Tajima T, et al.
    • Journal Title

      Journal of Pediatric Endocrinology and Metabolism 19

      Pages: 143-148

    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Two patients with Gitelman syndrome.2006

    • Author(s)
      Tajima T, et al.
    • Journal Title

      Clinical Pediatric Endocrinology 15

      Pages: 137-142

    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome2006

    • Author(s)
      Tajima T et al.
    • Journal Title

      Endocrine Journal 53

      Pages: 647-652

    • NAID

      10020613203

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Gitelman's syndrome with mental retardation.2006

    • Author(s)
      Morita R, Tajima T et al.
    • Journal Title

      Internal Medicine 45

      Pages: 211-213

    • NAID

      130000076573

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency : Implication for the backdoor pathway to dihydrotestosterone.2006

    • Author(s)
      Homma K, Tajima T. et al.
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 91

      Pages: 2643-2649

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Gitelman's syndrome with mental retardation.2006

    • Author(s)
      Morita R, Tajima T, et al.
    • Journal Title

      Internal Medicine 45

      Pages: 211-213

    • NAID

      130000076573

    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Novel TRPM6 Mutations in 21 Families with Primary Hypomagnesemia and Secondar Hypocalcemia.2005

    • Author(s)
      Schlingmann KP, Tajima T et al.
    • Journal Title

      Journal of American Society of Nephrology 16

      Pages: 3061-3069

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [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] Hypomagnesemia in a patient with Barth syndrome.2005

    • Author(s)
      TOSHIHIO TAJIMA
    • Journal Title

      Journal of Pediatric Endocrinology and Metabolism 18

      Pages: 523-523

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Two novel mutations in the thyroid peroxidase gene with goitrous hypothyroidism.2005

    • Author(s)
      Tajima T et al.
    • Journal Title

      Endocrine Journal 52

      Pages: 643-645

    • NAID

      10016782539

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [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] Transactivation function of -800 bp evolutionarily sonserved sequence at the SHOX 3' region. Implication for the downstream enhancer.2005

    • Author(s)
      Fukami M, Kato F, Tajima T, Yokoya S, Ogata T
    • Journal Title

      Am J Hum Genet 78・1

      Pages: 167-170

    • Data Source
      KAKENHI-PROJECT-16086202
  • [Journal Article] Two novel mutations in the thyroid peroxidase gene with goitrous hypothyroidism.2005

    • Author(s)
      TOSHIHIRO TAJIMA
    • Journal Title

      Endocrine Journal 52

      Pages: 643-645

    • NAID

      10016782539

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Hypomagnesemia in a patient with Barth syndrome.2005

    • Author(s)
      Tajima T et al.
    • Journal Title

      J Pediatric Endocrinology& Metabolism 18

      Pages: 523-523

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [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] Adrenal insufficiency2005

    • Author(s)
      Fujieda K, Tajima T
    • Journal Title

      Pediatric Research 57

      Pages: 62-69

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Transactivation function of -800 bp evolutionarily conserved sequence at the SHOX 3' region. Implication for the downstream enhancer.2005

    • Author(s)
      Fukami M, Tajima T et al.
    • Journal Title

      American Journal of Human Genetics 78

      Pages: 161-170

    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17591063
  • [Journal Article] Hypomagnesemia in a patient with Barth syndrome.2005

    • Author(s)
      Tajima T et al.
    • Journal Title

      J Pediatric Endocrinology& Metabolism 18

      Pages: 523-523

    • Data Source
      KAKENHI-PROJECT-17591063
  • [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] 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] 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] 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
  • [Presentation] 中枢性甲状線機能低下症とIGSF1異常症2016

    • Author(s)
      田島敏広
    • Organizer
      第59回日本甲状腺学会学術集会国際分子甲状腺学シンポジウム
    • Place of Presentation
      虎ノ門ヒルズフォーラム(東京都、港区)
    • Year and Date
      2016-11-03
    • Invited / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] 遺伝性 GHD/CPHD の進歩2015

    • Author(s)
      田島敏広
    • Organizer
      第49回日本小児内分泌学会学術総会
    • Place of Presentation
      タワーホール船堀(東京都、江戸川区)
    • Year and Date
      2015-10-08
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] 複合型下垂体機能低下症の成因2015

    • Author(s)
      田島敏広
    • Organizer
      第42回日本神経内分泌学会
    • Place of Presentation
      仙台市戦災復興記念館(宮城県、仙台市)
    • Year and Date
      2015-09-18
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] 妊娠期間中に甲状腺中毒症が顕性化した非自己免疫性甲状腺機能亢進症における機能獲得型TSH受容体遺伝子変異2014

    • Author(s)
      秋川 和聖, 小梁川 直秀, 越谷 剛, 田島 敏広
    • Organizer
      日本内分泌学会北海道地方会
    • Place of Presentation
      札幌医大臨床教育研究棟講堂,北海道、札幌市
    • Year and Date
      2014-11-01
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] Molecular basis of IGSF1 deficiency in Japan2014

    • Author(s)
      Tajima T, Nakamura A, Morikawa S
    • Organizer
      Pediatric Avademic Societies and Asian Society for Peditric Research JOint meeting
    • Place of Presentation
      Vancouver Convention Center (Canada)
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] IGSF1遺伝子異常による先天性中枢性甲状腺機能低下症の病態解明2013

    • Author(s)
      森川俊太郎、中村明枝、石津桂、母坪智行、依藤亨、田島敏広
    • Organizer
      第47回小児内分泌学会学術集会
    • Place of Presentation
      浅草ビューホテル 東京
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] Molecular basis of IGSF1 mutations in Japanese patients with X-linked congenital central hypothyroidism.2013

    • Author(s)
      Morikawa S, Nakamura A, Bak B, Silander TL, Lam J, Hotsubo T, Yorifuji T, Ishizu K, Bernard DJ, Tajima T.
    • Organizer
      The 9th Joint meeting, ESPE-LWPES in association with APEG, APPES, SLEP, JSPE
    • Place of Presentation
      MiLano Convention Center (Italy)
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] TSH受容体機能獲得型異常による甲状腺機能亢進症の1家系2011

    • Author(s)
      中村明枝、青柳隼人、石津桂、田島敏広
    • Organizer
      第20回臨床内分泌Up date
    • Place of Presentation
      札幌コンベンションセンター(北海道)
    • Year and Date
      2011-01-28
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 思春期発来異常へのアプローチ2011

    • Author(s)
      田島敏広
    • Organizer
      第20回臨床内分泌up date
    • Place of Presentation
      札幌
    • Year and Date
      2011-01-29
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 当院で経験したSepto-Optic Dysplasiaの2症例2011

    • Author(s)
      高梨久仁子, 高田晋, 越田慎一, 杉山未奈子, 野呂歩, 鈴木靖人, 仲西正憲, 永島哲郎, 田島敏広
    • Organizer
      第20回小児内分泌研究会
    • Place of Presentation
      札幌京王プラザホテル(北海道)
    • Year and Date
      2011-01-22
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 治療に難渋しアイソトープ治療をおこなった小児バセドウ病の3例2011

    • Author(s)
      石津桂、竹井俊樹、中村明枝、田島敏広
    • Organizer
      第20回臨床内分泌Up date
    • Place of Presentation
      札幌コンベンションセンター(北海道)
    • Year and Date
      2011-01-28
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 思春期発来異常へのアプローチ2011

    • Author(s)
      田島敏広
    • Organizer
      第20回臨床内分泌Up date
    • Place of Presentation
      札幌コンベンションセンター(北海道) 招待講演
    • Year and Date
      2011-01-29
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Cytochrome P450scc as a cause of congenital adrenal hyperplasia (lipoid CAH)2010

    • Author(s)
      田島敏広, 藤枝憲二
    • Place of Presentation
      京都
    • Year and Date
      2010-03-28
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] CHRGE症候群の4例2010

    • Author(s)
      中村明枝、石津桂、田島敏広
    • Organizer
      第44回日本小児内分泌学会学術集会
    • Place of Presentation
      大阪市中央会議堂(大阪府)
    • Year and Date
      2010-10-08
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Dr Kenji Fujieda Memorial Lecture2010

    • Author(s)
      田島敏広
    • Organizer
      49^<th> Annual Meeting of the European Society for Pediatric Endocrinology
    • Place of Presentation
      プラハ
    • Year and Date
      2010-09-24
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Congenital hypothyroidism caused by a PAX8 gene mutation manifested as sodium/iodide symporter gene defect.2010

    • Author(s)
      Jo W、Endo M, Ishizu K, Nakamura A, Tajima T
    • Organizer
      49^<th> Annual Meeting of the European Society for Pediatric Endocrinology
    • Place of Presentation
      プラハコンベンションセンター(チェコ)
    • Year and Date
      2010-09-25
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Longitudinal growth of patients with 21-hydroxylase deficiency.2010

    • Author(s)
      Nakamura A, Jo W, Ishizu K, Tajima T, Fujieda K
    • Organizer
      International Symposium on Pediatric Endocrinology
    • Place of Presentation
      東京
    • Year and Date
      2010-03-31
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Dr Kenji Fujieda Memorial Lecture2010

    • Author(s)
      Tajima T
    • Organizer
      49^<th> Annual Meeting of the European Society for Pediatric Endocrinology
    • Place of Presentation
      プラハコンベンションセンター(チェコ) 招待講演
    • Year and Date
      2010-09-24
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Molecular basis and clinical phenotypes caused by OTX2 gene defects in combined pituitary hormone deficiency.2010

    • Author(s)
      Tajima T, Nakamura A, Ishizu K, Jo W
    • Organizer
      14th International Congress of Endocrinology.
    • Place of Presentation
      京都
    • Year and Date
      2010-03-29
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Clinical and molecular genetic spectrum of lipoid CAH and noncalssic lipoid CAH.2009

    • Author(s)
      田島敏広, 藤枝憲二
    • Organizer
      LWPES/ESPE 8^<th> Joint Meeting Global Care in Pediatric Endocrinology
    • Place of Presentation
      ニューヨーク
    • Year and Date
      2009-09-13
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 思春期発来異常をめぐる諸問題2009

    • Author(s)
      田島敏広
    • Organizer
      第43回日本小児内分泌学会学術集会
    • Place of Presentation
      宇都宮、栃木県総合文化センター
    • Year and Date
      2009-10-03
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 新生児スクリーニングで見つかる先天性副腎過形成症-健やかな成長を目指して-2009

    • Author(s)
      田島敏広
    • Organizer
      第36回日本マススクリーニング学会
    • Place of Presentation
      札幌
    • Year and Date
      2009-08-21
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 先天性副腎過形成症のトランジッションについて2009

    • Author(s)
      田島敏広、藤枝憲二
    • Organizer
      第19回臨床内分泌代謝up date
    • Place of Presentation
      東京
    • Year and Date
      2009-03-14
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Clinical and molecular genetic spectrum of lipoid CAH and nonclassic lipoid CAH2009

    • Author(s)
      Tajima T, et al.
    • Organizer
      LWPES/ESPE 8^<th> Joint Meeting Global Care in Pediatric Endocrinology
    • Place of Presentation
      New York, Hilton hotel USA
    • Year and Date
      2009-09-13
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 思春期発来異常をめくる諸問題2009

    • Author(s)
      田島敏広
    • Organizer
      第43回日本小児内分泌学会学術集会
    • Place of Presentation
      宇都宮
    • Year and Date
      2009-10-03
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 新生児スクリーニングでみつかる先天性副腎過形-すこやかな成長を目指して-2009

    • Author(s)
      田島敏広
    • Organizer
      第36回日本マススクリーニング学会
    • Place of Presentation
      札幌、札幌エルプラザ
    • Year and Date
      2009-08-21
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 下垂体形成異常におけるOTX2の役割2008

    • Author(s)
      田島敏広、石津桂、星野正也、大竹明、雨宮伸、佐々木望、藤枝憲二
    • Organizer
      第81回日本内分泌学会学術総会
    • Place of Presentation
      青森
    • Year and Date
      2008-05-17
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 下垂体形成異常におけるOTX2の役割2008

    • Author(s)
      田島敏広, 他
    • Organizer
      第81回日本内分泌学会学術総会
    • Place of Presentation
      ホテル青森
    • Year and Date
      2008-05-17
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] Two novel mutations of the oTX2 causes anophthalmia, pituitary ectopic posterior lobe and combined pituitary hormone deficiency.2008

    • Author(s)
      Tajima T, Ishidu K, Otake A, Amamiya S, Kosaka K, Hoshino M
    • Organizer
      90^<th> annual meeting of Endocrine Society.
    • Place of Presentation
      サンフランシスコ
    • Year and Date
      2008-06-17
    • Data Source
      KAKENHI-PROJECT-20591213
  • [Presentation] 先天性下垂体疾患における新たな転写因子異常の展開2008

    • Author(s)
      田島敏広, 他
    • Organizer
      第42回日本小児内分泌学会学術集会
    • Place of Presentation
      米子コンベンションセンター
    • Year and Date
      2008-10-03
    • Data Source
      KAKENHI-PROJECT-20591213
  • [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] 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] 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] 副腎疾患のマススクリーニング、今後の展望2006

    • Author(s)
      田島敏広
    • Organizer
      第40回日本小児内分泌学会学術集会
    • Place of Presentation
      浜松
    • Year and Date
      2006-09-26
    • Data Source
      KAKENHI-PROJECT-16086202
  • [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] 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] 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] 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] 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] 先天性副腎機能異常の新展開

    • Author(s)
      田島敏広
    • Organizer
      第87回日本内分泌学会学術総会
    • Place of Presentation
      福岡国際会議場、福岡県、福岡市
    • Year and Date
      2014-04-23 – 2014-04-26
    • Invited
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] 先天性下垂体形成不全の4例

    • Author(s)
      田島敏広
    • Organizer
      第87回日本内分泌学会学術総会
    • Place of Presentation
      福岡国際会議場、福岡県、福岡市
    • Year and Date
      2014-04-23 – 2014-04-26
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] 福島原発事故前後の環境放射能と先天性甲状腺機能低下症の新生児マス・スクリーニング陽性率、精査率、濾紙血TSH値との関係

    • Author(s)
      南谷 幹史原田 正平, 長崎 啓祐, 安達 昌功, 安藏 慎, 石井 智弘, 鬼形 和道, 楠田 聡, 堀川 玲子, 水野 晴夫, 皆川 真規, 田島 敏広, 横谷 進, 福士 勝, 花井 潤師, 田崎 隆二, 山口 清次
    • Organizer
      第87回日本内分泌学会学術総会
    • Place of Presentation
      福岡国際会議場、福岡県、福岡市
    • Year and Date
      2014-04-23 – 2014-04-26
    • Data Source
      KAKENHI-PROJECT-25461380
  • [Presentation] IGSF1異常による中枢性甲状腺機能低下症の2例

    • Author(s)
      田島敏広
    • Organizer
      41 回日本マススクリーニング学会学術集会
    • Place of Presentation
      広島大学広仁会館,広島県、広島市
    • Year and Date
      2014-08-22 – 2014-08-23
    • Data Source
      KAKENHI-PROJECT-25461380
  • 1.  SUGAWARA Teruo (40250451)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 2.  TANAHASHI Yusuke (50374228)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 1 results
  • 3.  FUJIEDA Kenji (60173407)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 27 results
  • 4.  MUKAI Tokuo (50374799)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 4 results
  • 5.  OHMIYA Yoshihiro (20223951)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 6.  MORIYA kimihiko (20374233)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 7.  OKADA Tadashi (00326828)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 8.  ARIGA Tadashi (60322806)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 9.  SHINOHARA Nobuo (90250422)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results

URL: 

Are you sure that you want to link your ORCID iD to your KAKEN Researcher profile?
* This action can be performed only by the researcher himself/herself who is listed on the KAKEN Researcher’s page. Are you sure that this KAKEN Researcher’s page is your page?

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