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Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation.
Tanaka, Tatsuhiko; Oki, Eishin; Mori, Takayasu; Tsuruga, Kazushi; Sohara, Eisei; Uchida, Shinichi; Tanaka, Hiroshi.
Afiliación
  • Tanaka T; Department of Pediatrics, Hirosaki University Hospital, Aomori, Japan.
  • Oki E; Department of Pediatrics, Tsugaru General Hospital, Aomori, Japan.
  • Mori T; Department of Nephrology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Tsuruga K; Department of Pediatrics, Hirosaki University Hospital, Aomori, Japan.
  • Sohara E; Department of Nephrology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Uchida S; Department of Nephrology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Tanaka H; Department of Pediatrics, Hirosaki University Hospital, Aomori, Japan.
Nephrology (Carlton) ; 24(4): 489-490, 2019 Apr.
Article en En | MEDLINE | ID: mdl-30919533
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Seudohipoaldosteronismo / Receptores de Mineralocorticoides / Aldosterona Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child, preschool / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Nephrology (Carlton) Asunto de la revista: NEFROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Japón
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Seudohipoaldosteronismo / Receptores de Mineralocorticoides / Aldosterona Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child, preschool / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Nephrology (Carlton) Asunto de la revista: NEFROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Japón