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Contradiction between genetic analysis and diuretic loading test in type I Bartter syndrome: a case report.
Kuroda, Jumpei; Harada, Ryoko; Hamada, Riku; Okuda, Yusuke; Yoshida, Yasuhiro; Hataya, Hiroshi; Nozu, Kandai; Iijima, Kazumoto; Honda, Masataka; Ishikura, Kenji.
Afiliação
  • Kuroda J; Department of Nephrology and Neonatology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, Fuchu, Tokyo, 183-8561, Japan.
  • Harada R; Department of Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, Fuchu, Tokyo, 183-8561, Japan.
  • Hamada R; Department of Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, Fuchu, Tokyo, 183-8561, Japan. riku_hamada@tmhp.jp.
  • Okuda Y; Department of Pediatrics, Kitasato University School of Medicine, 1-15-1 Kitazato, Minami Ward, Sagamihara, Kanagawa, 252-0374, Japan.
  • Yoshida Y; Department of Pediatrics, Graduate School of Medicine, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo, 113-0033, Japan.
  • Hataya H; Department of Nephrology and General Pediatrics, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, Fuchu, Tokyo, 183-8561, Japan.
  • Nozu K; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, Hyogo, 650-0017, Japan.
  • Iijima K; Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, Hyogo, 650-0017, Japan.
  • Honda M; Department of Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, Fuchu, Tokyo, 183-8561, Japan.
  • Ishikura K; Department of Nephrology, Tokyo Metropolitan Children's Medical Center, 2-8-29 Musashidai, Fuchu, Tokyo, 183-8561, Japan.
BMC Nephrol ; 22(1): 295, 2021 08 30.
Article em En | MEDLINE | ID: mdl-34461850
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Bartter / Testes Genéticos / Diurese / Diuréticos Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child, preschool / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Bartter / Testes Genéticos / Diurese / Diuréticos Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Child, preschool / Humans / Male Idioma: En Ano de publicação: 2021 Tipo de documento: Article