Tajima Toshihiro 田島敏広

… Alternative Names

Researcher Number	50333597
Other IDs
External Links
Affiliation (Current)	2022: 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
Review Section/Research Field	Principal Investigator Pediatrics / Endocrinology / Pediatrics Except Principal Investigator Biological Sciences / Pediatrics
Keywords	Principal Investigator 下垂体 / NR5A1 / 小児内分泌学 / 発生 / CHD7 / 中枢性性腺機能低 / Septo-optic dysplasai / GLI2 / OTX2 / 複合型下垂体前葉ホルモン欠損 … More Except Principal Investigator 性分化異常症 (DSD) / 先天性副腎過形成症 / 先天性副腎低形成症 / 相互作用因子 / Antley-Bixler症候群 / POR異常症 / StAR / yeast two-hbrid screening / リポイド過形成症 / DAX-1 / 副腎低形成症 / Ad4BP-SF-1 / アンドロゲン不応症 / yeast two-hybrid screening / 精巣形成不全症 / SBP / 寡少精子症 / 遺伝子多型 / P450 oxidoreductase (POR) / Ad4BP / SFI / P450 oxidoreductase(POR) / 先天性副腎皮質過形成症(CAH) / WT1 / アンドロゲン受容体 / SOX9 / 複合型ステロイド合成障害 / 外陰部異常 / Yeast Two-hybrid Screening / 小児内分泌学 / 生物時計 / 思春期発来メカニズム / 時計遺伝子 / Kisspeptin / 思春期発来 / GnRH遺伝子 / 概日リズム / 発光レポーター測定 Less

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
  
  Clin Pediatr Endocrinol
  
  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] 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
  
  Clin Pediatr Endocrinol
  
  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] 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
  
  Clin Pediatr Endocrinol
  
  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] 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 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 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 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
- 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

Tajima Toshihiro 田島 敏広

TAJIMA Toshihiro 田島 敏広

Research Projects

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Co-Researchers

The mechanism of congenital central hypothyroidism caused by IGSF1 deficiencyPrincipal Investigator

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Functional and chronobiological analysis of factors for the timing of puberty in GnRH neurons

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Molecular basis of congenital pituitary defectPrincipal Investigator

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Analysis of Mechanism of Adrenal RegenerationPrincipal Investigator

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

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

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[Book] 中山書店2014

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[Book] 成長障害のマネージメント2013

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[Book] ワンランク上の小児の臨床検査2013

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[Book] 急性副腎不全 今日の治療指針2006

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[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

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[Journal Article] Neonatal mass screening for 21-hydroxylase deficiency2016

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[Journal Article] Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of <i>NR3C2</i>2015

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Tajima Toshihiro 田島敏広

TAJIMA Toshihiro 田島敏広

[Book] 急性副腎不全今日の治療指針2006