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Hemolytic uremic syndrome as the presenting manifestation of WT1 mutation and Denys-Drash syndrome: a case report.
Alge, Joseph L; Wenderfer, Scott E; Hicks, John; Bekheirnia, Mir Reza; Schady, Deborah A; Kain, Jamey S; Braun, Michael C.
Afiliação
  • Alge JL; Baylor College of Medicine, Department of Pediatrics, Pediatrician-Scientist Training and Development Program, Houston, TX, USA. joseph.alge@bcm.edu.
  • Wenderfer SE; Baylor College of Medicine, Department of Pediatrics, Renal Section, Houston, TX, USA.
  • Hicks J; Texas Children's Hospital, Houston, TX, USA.
  • Bekheirnia MR; Baylor College of Medicine, Department of Pathology and Immunology, Houston, TX, USA.
  • Schady DA; Texas Children's Hospital, Houston, TX, USA.
  • Kain JS; Baylor College of Medicine, Department of Molecular and Human Genetics, Houston, 77030, USA.
  • Braun MC; Baylor College of Medicine, Department of Pathology and Immunology, Houston, TX, USA.
BMC Nephrol ; 18(1): 243, 2017 Jul 18.
Article em En | MEDLINE | ID: mdl-28720077
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Denys-Drash / Proteínas WT1 / Síndrome Hemolítico-Urêmica / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Infant Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Denys-Drash / Proteínas WT1 / Síndrome Hemolítico-Urêmica / Mutação Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Infant Idioma: En Ano de publicação: 2017 Tipo de documento: Article