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Clinical characteristics of cytochrome P450 oxidoreductase deficiency: a nationwide survey in Japan.
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.
Afiliação
  • Yatsuga S; Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka 830-0011, Japan.
  • Amano N; Department of Pediatrics, Keio University, Tokyo 160-8582, Japan.
  • Nakamura-Utsunomiya A; Department of Pediatrics, Hiroshima University, Hiroshima 734-8553, Japan.
  • Kobayashi H; Department of Pediatrics, Shimane University, Shimane 693-0021, Japan.
  • Takasawa K; Department of Pediatrics, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
  • Nagasaki K; Department of Pediatrics, Niigata University Medical & Dental Hospital, Niigata 951-8122, Japan.
  • Nakamura A; Department of Pediatrics, Hokkaido University, Hokkaido 060-8638, Japan.
  • Nishigaki S; Department of Pediatrics, Osaka City University, Osaka 545-8585, Japan.
  • Numakura C; Department of Pediatrics, Yamagata University, Yamagata 990-9585, Japan.
  • Fujiwara I; Department of Pediatrics, Tohoku University, Miyagi 980-8575, Japan.
  • Minamitani K; Department of Pediatrics, Teikyo University Chiba Medical Center, Chiba 299-0111, Japan.
  • Hasegawa T; Department of Pediatrics, Keio University, Tokyo 160-8582, Japan.
  • Tajima T; Department of Pediatrics, Jichi Medical University, Tochigi 329-0498, Japan.
Endocr J ; 67(8): 853-857, 2020 Aug 28.
Article em En | MEDLINE | ID: mdl-32321882
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo de Síndrome de Antley-Bixler Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo de Síndrome de Antley-Bixler Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Newborn País/Região como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article