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SATO Naoko  佐藤 直子

… Alternative Names

NAOKO SATO  佐藤 直子

佐藤 直子  サトウ ナオコ

Sato Naoko  佐藤 直子

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Researcher Number 10383069
Other IDs
  • ORCIDhttps://orcid.org/0000-0001-5691-8089
Affiliation (Current) 2025: 東京大学, 医学部附属病院, 届出研究員
Affiliation (based on the past Project Information) *help 2023: 東京大学, 医学部附属病院, 届出研究員
2021: 東京大学, 医学部附属病院, 届出研究員
2018: 東京大学, 医学部附属病院, 登録研究員
2015: 東京大学, 医学部附属病院, 登録研究員
2014: 東京大学, 医学部附属病院, 登録研究医 … More
2013: 独立行政法人国立成育医療研究センター, その他部局等, 研究員
2012: 独立行政法人国立成育医療研究センター, その他部局等, 共同研究員
2010 – 2011: 独立行政法人国立成育医療研究センター, 分子内分泌研究部, 共同研究員
2009: National Research Institute for Child Health and Development, 小児思春期発育研究部, 共同研究員
2008: 国立成育医療センター(研究所), 小児思春期発育研究部, 研究員
2008: 国立成育医療センター研究所, 小児思春期発育研究部, 研究員
2006 – 2007: 国立成育医療センター研究所, 研究員
2004 – 2005: National Research Institute for Child Health and Development, Research Fellow, 研究員
2004: 国立成育医療センター研究所, 研究員
2004: 国立成育医療センター研究所, 小児思春期発育研究部, 研究員 Less
Review Section/Research Field
Principal Investigator
Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics / Endocrinology
Except Principal Investigator
Pediatrics / Biological Sciences
Keywords
Principal Investigator
先天性低ゴナドトロピン性性腺機能低下症 / 糖脂質代謝異常 / 遺伝子解析 / 少子化対策 / FGFR1 / GnRH / 肥満症 / 思春期発来 / 思春期遅発症 / 低身長症 … More / 中枢性性腺機能低下症 / 男性先天性中枢性性腺機能低下症 / 変異機能解析 / 治療効果 / 不妊 / 変異解析 / 性腺補充療法 / 次世代シーケンサー解析 / 男性先天性中枢性性腺機能 / 男性性腺機能低下症 / 治療ガイドライン / rFSH先行療法 / 低ゴナドトロピン性性腺機能低下症 / ゴナドトロピン療法 / 妊孕性獲得 / 先天性中枢性性線機能異常症 / 先天性中枢性性腺機能異常症 / 成人不妊 / 遺伝的異質性 / WAVEシステム / 標準的遺伝子診断法 / 遺伝子診断システム / DHPLC法 / 成人不妊症 … More
Except Principal Investigator
SHOX / Genotype-phenotype correlation / Lymphogenic gene / Gonadal function / Enhancer sequence / Haploinsufficiency / Sex choromosome / Turner syndrome / 遺伝子型-表現型解析 / リンパ管形成遺伝子 / 性腺機能 / 発現調節領域 / 半量不全 / 性染色体 / ターナー症候群 / POR / SF1 / Ad4BP / Nothシグナル伝達経路 / エストロゲン受容体α遺伝子 / Notchシグナル伝達経路 / 新規性分化異常症責任遺伝子 / 精巣形成不全 / 内分泌撹乱物質 / ヒト遺伝疾患 / 多因子疾患 / 単一遺伝子疾患 / 性分化異常症 Less
  • Research Projects

    (7 results)
  • Research Products

    (93 results)
  • Co-Researchers

    (8 People)
  •  代謝異常を伴うGnRH分泌不全の分子機構の解明:FGFシグナル伝達経路に着目してPrincipal Investigator

    • Principal Investigator
      佐藤 直子
    • Project Period (FY)
      2021 – 2023
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      The University of Tokyo
  •  Is the phosphodiesterase 3A gene involved in childhood growth and the onset of puberty?Principal Investigator

    • Principal Investigator
      NAOKO SATO
    • Project Period (FY)
      2018 – 2020
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      The University of Tokyo
  •  Elucidation of novel disease formation mechanism in glycolipid metabolism disorder with congenital hypogonadotropic hypogonadism.Principal Investigator

    • Principal Investigator
      Sato Naoko
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      The University of Tokyo
  •  Establishment of new diagnostic methods and therapeutic guidelines for congenital male hypogonadotropic hypogonadism.Principal Investigator

    • Principal Investigator
      SATO NAOKO
    • Project Period (FY)
      2012 – 2015
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      The University of Tokyo
      National Research Institute for Child Health and Development
  •  Elucidation of the pathogenic mechanism for the hypogonadotropic hypogonadism and the development of the standard mutation analyses system in congenital hypogonadotropic hypogonadism.Principal Investigator

    • Principal Investigator
      SATO Naoko
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Endocrinology
    • Research Institution
      National Research Institute for Child Health and Development
  •  Comprehensive mutation and susceptibility analyses and its clinical application in disorders of sex development and reproductive dysfunction

    • Principal Investigator
      OGATA Tsutomu
    • Project Period (FY)
      2004 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research on Priority Areas
    • Review Section
      Biological Sciences
    • Research Institution
      National Research Institute for Child Health and Development
  •  Clarification of genetic mechanisms leading to the whole phenotype in Turner syndrome

    • Principal Investigator
      OGATA Tsutomu
    • Project Period (FY)
      2003 – 2004
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      National Research Institute for Child Health and Development

All 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 2003 Other

All Journal Article Presentation Book

  • [Book] 低ゴナドトロピン性性腺機能低下症 小児内分泌学テキスト 第2版2016

    • Author(s)
      佐藤直子
    • Publisher
      日本小児内分泌学会編 診断と治療社
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Book] Kallmann症候群 神経疾患IV2014

    • Author(s)
      佐藤直子
    • Total Pages
      10
    • Publisher
      日本臨床社
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Book] 今日の小児治療指針(カルマン症候群の項)2012

    • Author(s)
      佐藤直子
    • Total Pages
      1028
    • Publisher
      医学書院
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Book] 今日の小児治療指針第15版Kallmann症候群2011

    • Author(s)
      佐藤直子
    • Publisher
      医学書院
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Book] 小児内分泌学・低ゴナドトロピン性性腺機能低下症2010

    • Author(s)
      佐藤直子
    • Total Pages
      9
    • Publisher
      日本小児内分泌学会
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Book] Prokineticin signaling pathwayとKallmam症候群医のあゆみ233(9)(第5土曜特集:G蛋白質共役受容体研究-疾患解明とシグナル制御の新時代)2010

    • Author(s)
      佐藤直子, 緒方勤
    • Total Pages
      4
    • Publisher
      医歯薬
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Book] 低ゴナドトロピン性性腺機能低下症の分子遺伝学的メカニズムと治療2010

    • Author(s)
      佐藤直子
    • Total Pages
      4
    • Publisher
      Life-Cycle Care
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Book] 低ゴナドトロピン性性腺機能低下症小児内分泌学テキスト日本小児内分泌学会編2010

    • Author(s)
      佐藤直子
    • Publisher
      診断と治療社
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Book] Pediatric Endocrine Reviews 抄訳シリーズ. No.232009

    • Author(s)
      佐藤直子
    • Total Pages
      2
    • Publisher
      ジャパンメディアートパブリッシング
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Book] 小児内分泌学テキスト 第1版(日本小児内分泌学会編)2009

    • Author(s)
      佐藤直子
    • Total Pages
      9
    • Publisher
      診断と治療社
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Book] 今日の小児治療指針 第15版 Kallmann症候群

    • Author(s)
      佐藤直子
    • Total Pages
      4
    • Publisher
      医学書院(印刷中)
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.2015

    • Author(s)
      Naoko Sato
    • Journal Title

      Clin Pediatr Endocrinol

      Volume: 24 Pages: 37-49

    • NAID

      130005069651

    • Data Source
      KAKENHI-PROJECT-15K09613
  • [Journal Article] Treatment situation of male hypogonadotropic hypogonadism in pediatrics and proposal of testosterone and gonadotropins replacement therapy protocols.2015

    • Author(s)
      Naoko Sato
    • Journal Title

      Clin Pediatr Endocrinol

      Volume: 24 Pages: 37-49

    • NAID

      130005069651

    • Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Journal Article] FGF受容体異常症2013

    • Author(s)
      佐藤直子
    • Journal Title

      ホルモンと臨床

      Volume: 7月 Pages: 513-526

    • Data Source
      KAKENHI-PROJECT-24591536
  • [Journal Article] Submicroscopic deletion involving the fibroblast growth factor receptor 1 gene in a patient with combined pituitary hormone deficiency.2013

    • Author(s)
      Fukami M, Iso M, Sato N
    • Journal Title

      Endocr J.

      Volume: May 9.

    • NAID

      10031195771

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Journal Article] 内分泌撹乱物質とヒト暴露のタイミング2012

    • Author(s)
      佐藤直子
    • Journal Title

      Pediatric Endocrinology Reviews

      Volume: No.29(印刷中)

    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Genetics of male hypogonadotropic hypogonadism2012

    • Author(s)
      Naoko Sato
    • Journal Title

      Pediatric Endocrinology Reviews

      Volume: (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Kallmann症候群の病因・病態2012

    • Author(s)
      佐藤直子
    • Journal Title

      日本生殖内分泌学会雑誌研究フロンテイア

      Volume: 第17号(in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Kallmann症候群の病因・病態2012

    • Author(s)
      佐藤直子
    • Journal Title

      日本生殖内分泌学会雑誌

      Volume: 第17号 Pages: 43-48

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Journal Article] Genetics of male hypogonadotropic hypogonadism.2012

    • Author(s)
      Sato N
    • Journal Title

      Pediatr Endocrinol Rev.

      Volume: Oct;10 1 Pages: 110-125

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Journal Article] 中枢性性腺機能低下症2011

    • Author(s)
      佐藤直子
    • Journal Title

      ホルモンと臨床別冊

      Volume: 58 Pages: 551-558

    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] 中枢性性腺機能低下症2011

    • Author(s)
      佐藤直子
    • Journal Title

      ホルモンと臨床

      Volume: 第58巻 Pages: 551-558

    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Hypothalamic dysfunction in a female with isolated hypogonadotropic hypogonadism and compound heterozygous TACR3 mutations and clinical manifestation in her heterozygous mother2010

    • Author(s)
      Sato N, 他4名
    • Journal Title

      Horm Res Peadiatr

      Volume: 773 Pages: 477-481

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Hypothalamic dysfunction in a female with isolated hypogonadotropic hypogonadism and compound heterozygous TACR3 mutations and clinical manifestation in her heterozygous mother.2010

    • Author(s)
      Fukami M, Sato N, et al.
    • Journal Title

      Horm Res Peadiatr

      Volume: 73 Pages: 477-481

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Prokineticin signaling pathwayとKallmann症候群2010

    • Author(s)
      佐藤直子、緒方勤
    • Journal Title

      医のあゆみ

      Volume: 233(9)

    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] 低ゴナドトロピン性性腺機能低下症の分子遺伝学的メカニズムと治療2010

    • Author(s)
      佐藤直子
    • Journal Title

      Life-Cycle Care

      Volume: Vol.7,No.1

    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype.2010

    • Author(s)
      Dateki S, Sato N, et al.
    • Journal Title

      J Clin Endocrinol Metab

      Volume: 95 Pages: 756-764

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Heterozygous OTX2 mutations are associated with variable pituitary phenotype2010

    • Author(s)
      Sato N, 他11名
    • Journal Title

      J Clin Endocrinol Metab

      Volume: 95 Pages: 756-764

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] Fezf1 is required for penetration of the basal lamina by olfactory axons to promote olfactory development2009

    • Author(s)
      Sato N, 他11名
    • Journal Title

      J Comp Neurol

      Volume: 515 Pages: 565-84

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] CHD7 mutations in patients initially diagnosed with Kallmann syndrome - the clinical overlap with CHARGE syndrome2009

    • Author(s)
      Ogata T(計10 名中4 番目), Sato N(計10名中5 番目), Claahsen-van der Grinten HL, van der Donk K, Seminara S, Bergman JE, Brunner HG, Crowley WF Jr, Hoefsloot LH
    • Journal Title

      Clinical Genetics 75 (1)

      Pages: 65-71

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] 中枢性性腺機能不全: Kallmann症候群を主として2009

    • Author(s)
      佐藤直子,緒方勤
    • Journal Title

      ゲノム医学

      Volume: 9(2) Pages: 67-70

    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] CHD7 mutations in patients initially diagnosed with Kallmann syndrome-the clinical overlap with CHARGE syndrome2009

    • Author(s)
      Sato N, 他11名
    • Journal Title

      ClinicalGenetics

      Volume: 75 Pages: 65-71

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Journal Article] OTX2 Mutation in a patient with anophthalmia, short stature, and partial GH deficiency: functional studies using the IRBP, HESX1, and POU1F1 promoters2008

    • Author(s)
      Dateki S, Fukami M, Sato N, Muroya K, Adachi M, Ogata T
    • Journal Title

      Journal of Clinical Endocrinology & Metabolism 9号(10

      Pages: 3697-702

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] OTX2 Mutation in a patient with anophthalmia, short stature, and partial GH deficiency: functional studies using the IRBP, HESX1, and POU1F1 promoters2008

    • Author(s)
      Dateki S, Fukami M, Sato N, Muroya K, Adachi M, Ogata T
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 93 (10)

      Pages: 3697-702

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Hypogonadotropic hypogonadism in an adult female with heterozygous hypomorphic mutation of SOX22007

    • Author(s)
      Sato N(筆頭), Ogata T(計7 名中最終)
    • Journal Title

      European Journal of Endocrinology 156 (2)

      Pages: 167-171

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Somatic and germline mutations of the fibroblast growth factor receptor 1 gene in a mother and the son: implication for apparently mutation negative Kallmann syndrome2006

    • Author(s)
      Sato N, Ohyama K, Fukami M, Okada M, Ogata T
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 91 (4)

      Pages: 1415-1418

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Somatic and germline mutations of the fibroblast growth factor receptor 1 gene in a mother and the son : implication for apparently mutation negative Kallmann syndrome2006

    • Author(s)
      Sato N, Ohyama K, Fukami M, Okada M, Ogata T
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 91(4)

      Pages: 1415-1418

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Gonadotropin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1 : report of three families2005

    • Author(s)
      Sato N, Hasegawa T, Hori N, Fukami M, Yoshimura Y, Ogata T
    • Journal Title

      Human Reproduction 120(8)

      Pages: 2173-2178

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.2005

    • Author(s)
      Fukami, M., Horikawa, R., Nagai, T., Tanaka, T., Naiki, Y., Sato, N., Okuyama, T., Nakai, H., Soneda, S., Tachibana, K., Matsuo, N., Sato, S., Homma, K., Nishimura, G., Hasegawa, T., Ogata, T.
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 90

      Pages: 414-426

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591150
  • [Journal Article] Gonadotropin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families2005

    • Author(s)
      Sato N, Hasegawa T, Hori N, Fukami M, Yoshimura Y, Ogata T
    • Journal Title

      Human Reproduction 20 (8)

      Pages: 2173-2178

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Premature ovarian failure in a female with proximal symphalangism and NOG mutation.2004

    • Author(s)
      Kosaki, K., Sato, S., Hasegawa, T., Matsuo, N., Suzuki, T., Ogata, T.
    • Journal Title

      Fertility and Sterility 81(4)

      Pages: 1137-1139

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591150
  • [Journal Article] Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients2004

    • Author(s)
      Sato N, Katsumata N, Ogata T, et al.
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 89(3)

      Pages: 1079-1088

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Testicular dysgenesis without adrenal insufficiency in a 46, XY patient with a heterozygous inactive mutation of steroidogenic factor-12004

    • Author(s)
      Hasegawa T, Fukami_M, Sato N, Sasaki G, Fukutani K, Morohashi K, Ogata T
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 89(12)

      Pages: 5930-5935

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Testicular dysgenesis without adrenal insufficiency in a 46,XY patient with a heterozygous inactive mutation of steroidogenic factor-12004

    • Author(s)
      Hasegawa T, Fukami M, Sato N, Sasaki G, Fukutani K, Morohashi K, Ogata T
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 89

      Pages: 5930-5935

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients2004

    • Author(s)
      Sato N(筆頭), Ogata T(計19 名中最終)
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism 89 (3)

      Pages: 1079-1088

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Journal Article] Lymphstasis in a boy with Noonan syndrome: implication for the development of skeletal features.2003

    • Author(s)
      Ogata, T., Sato, S., Hasegawa, T., Kosaki, K.
    • Journal Title

      Endocrine Journal 50(3)

      Pages: 319-324

    • NAID

      130004443046

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591150
  • [Journal Article] Longitudinal auxological study in a female with SHOX haploinsufficiency and normal ovarian function.2003

    • Author(s)
      Fukami, M., Matsuo, N., Hasegawa, T., Sato, S., Ogata, T.
    • Journal Title

      European Journal of Endocrinology 149(4)

      Pages: 337-341

    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-15591150
  • [Journal Article] Somatic and germline mutations of the fibroblast growth factor receptor 1 gene in a mother and the son : implication for apparently mutation negative Kallmann syndrome

    • Author(s)
      Sato N, Ohyama K, Fukami M, Okada M, Ogata T
    • Journal Title

      Journal of Clinical Endocrinology and Metabolism (In press)

    • Data Source
      KAKENHI-PROJECT-16086215
  • [Presentation] rFSH先行療法の治療経験:先天性男性中枢性性腺機能低下症の妊孕性獲得に対する新しい治療法の試み2015

    • Author(s)
      佐藤直子
    • Organizer
      第49回小児内分泌学会学術集会
    • Place of Presentation
      船堀タワーホール(東京都・江戸川区)
    • Year and Date
      2015-10-08
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] FSH先行療法の治療経験:先天性男性中枢性性腺機能低下症の妊孕性獲得に対する新しい治療法の試み 船堀2015 10月8日2015

    • Author(s)
      佐藤直子
    • Organizer
      第49回小児内分泌学会学術集
    • Place of Presentation
      船堀タワーセンター(東京・江戸川区)
    • Year and Date
      2015-10-08
    • Data Source
      KAKENHI-PROJECT-15K09613
  • [Presentation] 先天性男性中枢性性腺機能低下症:rFSH先行療法の試み2015

    • Author(s)
      佐藤直子
    • Organizer
      第25回臨床内分泌update学会学術集会
    • Place of Presentation
      東京国際フォーラム(東京都・千代田区)
    • Year and Date
      2015-11-27
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] 先天性男性中枢性性腺機能低下症:rFSH先行療法の試み 東京2015 11月27日2015

    • Author(s)
      佐藤直子
    • Organizer
      第25回臨床内分泌update学会学術集会
    • Place of Presentation
      東京国際フォーラム (東京・千代田区)
    • Year and Date
      2015-11-27
    • Data Source
      KAKENHI-PROJECT-15K09613
  • [Presentation] ゴナドトロピン補充療法に対する中枢性男性性腺機能低下症患者の長期治療経過。2013

    • Author(s)
      佐藤直子
    • Organizer
      第86回日本内分泌学会総会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] 男性低ゴナドトロピン性性腺機能低下症の成人身長と精液検査に関するアンケート調査2013

    • Author(s)
      佐藤直子
    • Organizer
      第47回日本小児内分泌学会学術集会
    • Place of Presentation
      東京 浅草
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] Hypogonadotropic hypogonadism and the gene for fibroblast growth factor receptor 12013

    • Author(s)
      Naoko Sato
    • Organizer
      9th Joint Meeting of Pediatric Endocrinology
    • Place of Presentation
      イタリア ミラノ
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] 次世代遺伝子解析技術を用いた性成熟異常症60例の病因解析2013

    • Author(s)
      佐藤直子
    • Organizer
      日本人類遺伝学会第58回大会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] ゴナドトロピン補充療法に対する先天性中枢性男性性腺機能低下症患者の長期治療成績と治療効果2013

    • Author(s)
      佐藤直子
    • Organizer
      第18回日本生殖内分泌学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] ゴナドトロピン補充療法に対する先天性中枢性男性性腺機能低下症患者の長期治療成績と治療効果2013

    • Author(s)
      佐藤直子
    • Organizer
      第47回日本小児内分泌学会学術集会
    • Place of Presentation
      東京 浅草
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] ゴナドトロピン補充療法に対する中枢性男性性腺機能低下症患者の長期治療経過。2013

    • Author(s)
      佐藤直子
    • Organizer
      第86回日本内分泌学会
    • Place of Presentation
      仙台
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] Kallmann症候群の病因・病態にoligogenicityが関与する。2012

    • Author(s)
      佐藤直子
    • Organizer
      第85回日本内分泌学会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] Kallmann症候群の病因・病態にoligogenicityが関与する2012

    • Author(s)
      佐藤直子、勝又規行、緒方勤
    • Organizer
      第45回日本内分泌学会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] ゴナドトロピン補充療法と生殖補助医療の併用により挙児に至った中枢性性腺機能低下症患者の一例。2012

    • Author(s)
      佐藤直子
    • Organizer
      第46回小児内分泌学会
    • Place of Presentation
      大阪
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] ゴナドトロピン補充療法と生殖補助医療の併用により挙児に至った中枢性性腺機能低下症患者の一例2012

    • Author(s)
      佐藤直子
    • Organizer
      第57回人類遺伝学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] ゴナドトロピン補充療法に対する中枢性男性性腺機能低下症患者の長期治療経過2011

    • Author(s)
      佐藤直子、堀川玲子、内木康博、田中敏章
    • Organizer
      第45回小児内分泌学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群の病因・病態にoligogenicityが関与する2011

    • Author(s)
      佐藤直子、勝又規行、緒方勤
    • Organizer
      第45回小児内分泌学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] 男児性腺補充療法2011

    • Author(s)
      佐藤直子
    • Organizer
      三重県小児内分泌代謝研究会
    • Place of Presentation
      三重県
    • Year and Date
      2011-07-21
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Molecular genetics of hypogonadotropic hypogonadism2011

    • Author(s)
      Naoko Sato
    • Organizer
      The Fourteenth Lilly International Symposium. Growth and Sexual Development Part II
    • Place of Presentation
      Tokyo
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群の病因・病態にoligogenicityが関与する2011

    • Author(s)
      佐藤直子、勝又規行、緒方勤
    • Organizer
      第56回人類遺伝学会
    • Place of Presentation
      千葉
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Molecular genetics of hypogonadotropic hypogonadism2011

    • Author(s)
      Naoko Sato
    • Organizer
      The Fourteenth Lilly International Symposium. Growth and Sexual Development Part II
    • Place of Presentation
      東京
    • Year and Date
      2011-10-29
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] 男児性腺補充療法2011

    • Author(s)
      佐藤直子
    • Organizer
      三重県小児内分泌代謝研究会
    • Place of Presentation
      三重
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群の病因・病態にoligogenicityが関与する2011

    • Author(s)
      佐藤直子、勝又規行、緒方勤
    • Organizer
      第16回日本生殖内分泌学会
    • Place of Presentation
      東京
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群患者におけるFGFR1 acid box変異は,神経繊維伸展を障害する2010

    • Author(s)
      佐藤直子、瀬尾美鈴、寺田基剛、上牧務、緒方勤
    • Organizer
      第43回日本内分泌学会,第83回日本内分泌学会学術総会
    • Year and Date
      2010-03-26
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群115例における分子遺伝学的および臨床学的解析2010

    • Author(s)
      佐藤直子
    • Organizer
      第113回日本小児科学会
    • Place of Presentation
      岩手
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群兄弟例における成長促進療法と性腺補充療法2010

    • Author(s)
      佐藤直子、田中敏章
    • Organizer
      第44回日本小児内分泌学会
    • Place of Presentation
      大阪
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] 低ゴナドトロピン性性腺機能低下症女性におけるTACR3変異の同定と臨床像の解析2010

    • Author(s)
      深見真紀, 佐藤直子
    • Organizer
      第113回日本小児科学会
    • Place of Presentation
      盛岡
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群兄弟例における成長促進療法と性腺補充療法2010

    • Author(s)
      佐藤直子
    • Organizer
      第44回日本小児内分泌学会
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群患者におけるFGFR1 acid box一アミノ酸挿入変異はFGF依存性に神経線維伸展を障害する2010

    • Author(s)
      佐藤直子、瀬尾美鈴
    • Organizer
      第83回日本内分泌学会
    • Place of Presentation
      京都
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann syndrome : a one amino-acid insertion mutation of the fibroblast growth factor receptor 1(FGFR1) acid box may affect neuronal extension in an FGF-dependent manner. In : Normal and Abnormal Pubertal Development2010

    • Author(s)
      Naoko Sato
    • Organizer
      The 14th International Congress of Endocrinology
    • Place of Presentation
      Tokyo
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群115例における分子遺伝学的および臨床学的解析2010

    • Author(s)
      佐藤直子
    • Organizer
      第113回日本小児科学会
    • Place of Presentation
      盛岡
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Recent Progress in Hypogonadotropic Hypogonadism2010

    • Author(s)
      佐藤直子
    • Organizer
      14^<th> International Congress of Endocrinology(ICE2010)2010.SY-13-1-4
    • Place of Presentation
      Kyoto, Japan
    • Year and Date
      2010-03-29
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann syndrome : a one amino-acid insertion mutation of the fibro blast growth factor receptor 1(FGFR1)acid box may affect neuronal extension in an FGF-dependent manner.In : Normal and Abnormal Pubertal Development.The International Symposium on Pediatric Endocrinology.2010

    • Author(s)
      Sato N
    • Organizer
      The 14th International Congress of Endocrinology.
    • Place of Presentation
      Tokyo, Japan.
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Recent progress in hypogonadotropic hypogonadism2010

    • Author(s)
      Naoko Sato
    • Organizer
      The 14th International Congress of Endocrinology
    • Place of Presentation
      Kyoto
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann 症候群患者におけるFGFR1 acid box 変異は, 神経繊維伸展を障害する2010

    • Author(s)
      佐藤直子, 他
    • Organizer
      第83回日本内分泌学会学術総会
    • Place of Presentation
      京都
    • Year and Date
      2010-03-26
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann 症候群患者におけるFGFR1 acid box 変異は, 神経繊維伸展を障害する2009

    • Author(s)
      佐藤直子, 他
    • Organizer
      第54回日本人類遺伝学会
    • Place of Presentation
      東京
    • Year and Date
      2009-09-25
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群(KS) FGFR1 acid box変異は,神経繊維伸展を障害する2009

    • Author(s)
      佐藤直子、瀬尾美鈴、寺田基剛、上牧務、緒方勤
    • Organizer
      第54回日本人類遺伝学会
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann症候群患者におけるFGFR1 acid box変異は,神経繊維伸展を障害する2009

    • Author(s)
      佐藤直子,瀬尾美鈴,寺田基剛,上牧務,緒方勤
    • Organizer
      第43回日本小児内分泌学会
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] Kallmann 症候群患者におけるFGFR1 acid box 変異は, 神経繊維伸展を障害する2009

    • Author(s)
      佐藤直子, 他
    • Organizer
      第43回日本小児内分泌学会
    • Place of Presentation
      宇都宮
    • Year and Date
      2009-10-02
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] ゴナドトロピン補充療法に対する先天性中枢性男性性腺機能低下症患者の長期治療成績と治療効果

    • Author(s)
      佐藤直子
    • Organizer
      第87回日本内分泌学会総会
    • Place of Presentation
      福岡
    • Year and Date
      2014-04-24 – 2014-04-26
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] 次世代遺伝子解析技術を用いた性成熟異常症60例の病因解析「低ゴナドトロピン性性腺機能低下症を中心に」

    • Author(s)
      佐藤直子
    • Organizer
      第87回日本内分泌学会総会
    • Place of Presentation
      福岡
    • Year and Date
      2014-04-24 – 2014-04-26
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] 小児期早期に診断された男性低ゴナドトロピン性性腺機能低下症の治療指針の提案

    • Author(s)
      佐藤直子
    • Organizer
      第48回日本小児内分泌学会学術集会
    • Place of Presentation
      静岡 浜松
    • Year and Date
      2014-09-25 – 2014-09-27
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] 低ゴナドトロピン性性腺機能低下症女性におけるTACR3変異の同定と臨床像の解析

    • Author(s)
      深見真紀、佐藤直子
    • Data Source
      KAKENHI-PROJECT-21591188
  • [Presentation] 小児期早期に診断された男性低ゴナドトロピン性性腺機能低下症の治療指針の提案

    • Author(s)
      佐藤直子
    • Organizer
      日本人類遺伝学会第58回大会
    • Place of Presentation
      東京 船堀
    • Year and Date
      2014-11-19 – 2014-11-22
    • Data Source
      KAKENHI-PROJECT-24591536
  • [Presentation] 自然に性腺機能低下症が回復した複合型下垂体機能低下症の2例

    • Author(s)
      佐藤直子
    • Organizer
      第48回日本小児内分泌学会学術集会
    • Place of Presentation
      静岡 浜松
    • Year and Date
      2014-09-25 – 2014-09-27
    • Data Source
      KAKENHI-PROJECT-24591536
  • 1.  SEO Misuzu (60211223)
    # of Collaborated Projects: 4 results
    # of Collaborated Products: 0 results
  • 2.  OGATA Tsutomu (40169173)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 17 results
  • 3.  FUKAMI Maki (40265872)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 11 results
  • 4.  田中 敏章 (90142067)
    # of Collaborated Projects: 2 results
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  • 5.  KATSUMATA Noriyuki (10260340)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 6.  DATEKI Sumito (70462801)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 7.  KITANAKA Sachiko (30431638)
    # of Collaborated Projects: 1 results
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  • 8.  門脇 弘子 (50161146)
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