Personnel Information

写真a

TAKASAWA Kei


Job title

Assistant Professor

Mail Address

ktakasawa.ped@tmd.ac.jp

Graduating School 【 display / non-display

  • Tokyo Medical and Dental University, Faculty of Medicine, 2003.03, Graduated

Graduate School 【 display / non-display

  • Tokyo Medical and Dental University, Doctor's Course, 2014.03, Completed

Campus Career 【 display / non-display

  • 2015.04
    -
    2016.05
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Medical and Dental Sciences, Bio-Environmental Response, Pediatrics and Developmental Biology, Visiting Lecturer
  • 2016.06
    -
    2017.03
    Tokyo Medical and Dental University, Medical Hospital, Hospital Departments, Department of Pediatrics, Maternal and Woman's Medicine, Pediatrics, Visiting Lecturer
  • 2017.04
    -
    2018.03
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Medical and Dental Sciences, Bio-Environmental Response, Pediatrics and Developmental Biology, Assistant Professor
  • 2018.04
    -
    Now
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Medical and Dental Sciences, Bio-Environmental Response, Pediatrics and Developmental Biology, Assistant Professor
  • 2018.07
    -
    2019.03
    Tokyo Medical and Dental University, Graduate School of Medical and Dental Sciences, Endowed Departments, Department of Child Health and Development, Assistant Professor
 

Published Papers & Misc 【 display / non-display

  • Gau Maki, Konishi Kaoru, Takasawa Kei, Nakagawa Ryuichi, Tsuji-Hosokawa Atsumi, Hashimoto Atsuko, Sutani Akito, Tajima Toshihiro, Hasegawa Tomonobu, Morio Tomohiro, Kashimada Kenichi. The progression of salt-wasting and the body weight change during the first 2 weeks of life in classical 21-hydroxylase deficiency patients. CLINICAL ENDOCRINOLOGY. 2021.02; 94 (2): 229-236. ( DOI )

  • Kei Takasawa, Yuichi Miyakawa, Yoko Saito, Eriko Adachi, Tsunanori Shidei, Akito Sutani, Maki Gau, Ryuichi Nakagawa, Atsuko Taki, Kenichi Kashimada, Tomohiro Morio. Marked clinical heterogeneity in congenital hyperinsulinism due to a novel homozygous ABCC8 mutation. Clin Endocrinol (Oxf). 2021.02; ( PubMed, DOI )

  • Nozomi Matsuda, Kei Takasawa, Yasuhisa Ohata, Shigeru Takishima, Takuo Kubota, Yasuki Ishihara, Makoto Fujiwara, Erika Ogawa, Tomohiro Morio, Kenichi Kashimada, Keiichi Ozono. Potential pathological role of single nucleotide polymorphism (c.787T>C) in alkaline phosphatase (ALPL) for the phenotypes of hypophosphatasia. Endocr. J.. 2020.12; 67 (12): 1227-1232. ( PubMed, DOI )

  • Takeru Yamauchi, Masatoshi Imamura, Kei Takasawa, Keisuke Nakajima, Ryuichi Nakagawa, Maki Gau, Manabu Sugie, Atsuko Taki, Masahiko Kawai, Kenichi Kashimada, Tomohiro Morio. Prematurity at less than 24 weeks of gestation is a risk for prolonged hyperglycemia in extremely low-birth weight infants. Endocrine. 2020.10; 70 (1): 71-77. ( PubMed, DOI )

  • Yatsuga Shuichi, Amano Naoko, Nakamura-Utsunomiya Akari, Kobayashi Hironori, Takasawa Kei, Nagasaki Keisuke, Nakamura Akie, Nishigaki Satsuki, Numakura Chikahiko, Fujiwara Ikuma, Minamitani Kanshi, Hasegawa Tomonobu, Tajima Toshihiro. Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan. ENDOCRINE JOURNAL. 2020.08; 67 (8): 853-857. ( DOI )

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Conference Activities & Talks 【 display / non-display

  • Takasawa K. Patient choice of growth hormone device improves child and adolescent adherence, and effects of growth hormone therapy. Novo Nordisk Global Expert Panel Meeting: Role of Patient Autonomy and Shared Decision Making 2017.10.08 London, UK

  • Takasawa K, Igarashi M, Takada S, Yamataka A, Ogata T, Fukami M, Kashimada K. Various phenotypes of 46, XX DSD due to the p.R92W variant of NR5A1. The 51st Annual Scientific Meeting of JSPE 2017.09.30 Osaka

  • Takasawa K, Tsuji A, Nomura R, Miyakawa Y, Numakura C, Kashimada K, Morio T. Molecular mechanism of insulin resistance: two cases of insulin receptoropathy. The 120th Annual Meeting of the JPS 2017.02.01 Tokyo

  • Kei Takasawa, et al.. Mortality and incidence of misidentification of sex assignment in patients with congenital 21-hydroxylase deficiency identified by a newborn screening program in Japan (2001-2015).. The 9th biennial scientific meeting of the Asia Pacific Paediatric Endocrine Society 2016.11.18 Tokyo, Japan

  • Maki Igarashi, Kei Takasawa, Akiko Hakoda, Junko Kanno, Shuji Takada, Mami Miyado, Toshihiro Tajima, Ryohei Sekido, Tsutomu Ogata, Kenichi Kashimada, Maki Fukami. Identical NR5A1 Missense Mutations in Two Unrelated 46, XX Individuals with Testicular Tissues. The 9th Biennial Scientific Meeting of the Asia Pacific Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

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Awards & Honors 【 display / non-display

  • International Society of Endocrinology (ISE) Travel Grant,International Society of Endocrinology ,2014.06