Katsumata Noriyuki

カツマタノリユキ | Katsumata Noriyuki

Affiliation and department：
Job title： Research associate

Research field (1)： Fetal medicine/Pediatrics

Research keywords (2)：分子内分泌学 , 小児内分泌学

Research theme for competitive and other funds (10)：

2019 - 2022 Development of gene therapy for congenital adrenal hyperplasia using AAV vectors and iPS cells
2017 - 2022 Exploration of novel causative genes for adrenal hypoplasia congenital and familial isolated glucocorticoid deficiency
2016 - 2019 Development of gene therapy for congenital adrenal hyperplasia using AAV vectors and iPS cells
2013 - 2016 Extra-Adrenal Induction of Cyp21a1 Ameliorates Systemic Steroid Metabolism in a Mouse Model of Congenital Adrenal Hyperplasia
2010 - 2013 Extra-adrenal expression of Cyp21a1 for gene therapy of congenital adrenal hyperplasia

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Papers (136)：

Naoko Amano, Satoshi Narumi, Katsuya Aizu, Mari Miyazawa, Kohji Okamura, Hirofumi Ohashi, Noriyuki Katsumata, Tomohiro Ishii, Tomonobu Hasegawa. Single-Exon Deletions of ZNRF3 Exon 2 Cause Congenital Adrenal Hypoplasia. The Journal of Clinical Endocrinology & Metabolism. 2023
Yasuhiro Naiki, Mami Miyado, Miyuki Shindo, Reiko Horikawa, Yuichi Hasegawa, Noriyuki Katsumata, Shuji Takada, Hidenori Akutsu, Masafumi Onodera, Maki Fukami. AAV-mediated gene therapy for patients' fibroblasts, iPS cells, and a mouse model of congenital adrenal hyperplasia. Human gene therapy. 2022. 33. 15-16. 801-809
田島敏広, 長谷川奉延, 石井智弘, 鹿島田健一, 高澤啓, 勝又規行, 棚橋祐典, 向井徳男. 今知っておきたい新生児マススクリーニングの進歩先天性副腎過形成症スクリーニングの現状と課題. 日本小児科学会雑誌. 2021. 125. 2. 156-156
Shinsuke Onuma, Tomoya Fukuoka, Yoko Miyoshi, Miho Fukui, Yoshinori Satomura, Kie Yasuda, Takeshi Kimura, Makiko Tachibana, Kazuhiko Bessho, Takehisa Yamamoto, et al. Two girls with a neonatal screening-negative 21-hydroxylase deficiency requiring treatment with hydrocortisone for virilization in late childhood. Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology. 2021. 30. 3. 143-148
Tomohiro Ishii, Toshihiro Tajima, Kenichi Kashimada, Tokuo Mukai, Yusuke Tanahashi, Noriyuki Katsumata, Junko Kanno, Takashi Hamajima, Kenichi Miyako, Shinobu Ida, et al. Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form Revisited. The Journal of clinical endocrinology and metabolism. 2020. 105. 11

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MISC (73)：

福岡智哉, 三善陽子, 大沼真輔, 和田珠希, 里村宜紀, 安田紀惠, 山本景子, 木村武司, 橘真紀子, 別所一彦, et al. 男性化徴候を契機に診断された非古典型21水酸化酵素欠損症の一例. 日本内分泌学会雑誌. 2018. 94. 2. 615-615
福岡智哉, 三善陽子, 和田珠希, 山本景子, 橘真紀子, 山本威久, 勝又規行, 本間桂子, 長谷川奉延, 大薗恵一. 新生児マススクリーニングで発見されず男性化徴候から10歳時に診断された非古典型先天性副腎過形成症の一例. 日本内分泌学会雑誌. 2017. 93. 4. 1295-1295
Congenital Unresponsiveness to Adrenocorticotropin (ACTH). 2016. 71. 10. 1965-1968
鳴海覚志, 天野直子, 石井智弘, 勝又規行, 福澤龍二, 芝田晋介, 岡野栄之, 清水厚志, 三宅紀子, 松本直通, et al. 稀少疾患の分子病態メカニズムエンドソーム系の平衡の破綻機能亢進型SAMD9変異によるMIRAGE症候群. 日本生化学会大会・日本分子生物学会年会合同大会講演要旨集. 2015. 88回・38回. [1W5-p
鳴海覚志, 天野直子, 石井智弘, 勝又規行, 福澤龍二, 清水厚志, 三宅紀子, 松本直通, 長谷川奉延. MIRAGE症候群:機能亢進型SAMD9変異を原因とする新規症候群の発見. 日本内分泌学会雑誌. 2015. 91. 3. 792

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Education (1)：

- 1981 The University of Tokyo Faculty of Medicine School of Medicine

Professional career (1)：

医学博士 (浜松医科大学)

Committee career (2)：

日本小児内分泌学会評議員
日本内分泌学会評議員

Association Membership(s) (4)：

米国内分泌学会 , 日本小児内分泌学会 , 日本内分泌学会 , 日本小児科学会

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