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Marked clinical heterogeneity in congenital hyperinsulinism due to a novel homozygous ABCC8 mutation.
Takasawa, Kei; Miyakawa, Yuichi; Saito, Yoko; Adachi, Eriko; Shidei, Tsunanori; Sutani, Akito; Gau, Maki; Nakagawa, Ryuichi; Taki, Atsuko; Kashimada, Kenichi; Morio, Tomohiro.
Afiliación
  • Takasawa K; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Miyakawa Y; Department of Pediatrics, Kawaguchi Municipal Medical Center, Kawaguchi, Japan.
  • Saito Y; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Adachi E; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Shidei T; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Sutani A; Department of Pediatrics, Kawaguchi Municipal Medical Center, Kawaguchi, Japan.
  • Gau M; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Nakagawa R; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Taki A; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Kashimada K; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
  • Morio T; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan.
Clin Endocrinol (Oxf) ; 94(6): 940-948, 2021 06.
Article en En | MEDLINE | ID: mdl-33595839
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hiperinsulinismo Congénito Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Clin Endocrinol (Oxf) Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hiperinsulinismo Congénito Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Clin Endocrinol (Oxf) Año: 2021 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido