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Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome.
Palazzo, Viviana; Raglianti, Valentina; Landini, Samuela; Cirillo, Luigi; Errichiello, Carmela; Buti, Elisa; Artuso, Rosangela; Tiberi, Lucia; Vergani, Debora; Dirupo, Elia; Romagnani, Paola; Mazzinghi, Benedetta; Becherucci, Francesca.
Afiliação
  • Palazzo V; Medical Genetics Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Raglianti V; Department of Biomedic, Experimental and Clinical Sciences "Mario Serio", University of Florence, 50139 Florence, Italy.
  • Landini S; Nephrology and Dialysis Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Cirillo L; Medical Genetics Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Errichiello C; Department of Biomedic, Experimental and Clinical Sciences "Mario Serio", University of Florence, 50139 Florence, Italy.
  • Buti E; Nephrology and Dialysis Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Artuso R; Nephrology and Dialysis Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Tiberi L; Nephrology and Dialysis Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Vergani D; Medical Genetics Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Dirupo E; Medical Genetics Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Romagnani P; Medical Genetics Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Mazzinghi B; Medical Genetics Unit, Meyer Children's Hospital, 50139 Florence, Italy.
  • Becherucci F; Department of Biomedic, Experimental and Clinical Sciences "Mario Serio", University of Florence, 50139 Florence, Italy.
Int J Mol Sci ; 23(10)2022 May 18.
Article em En | MEDLINE | ID: mdl-35628451
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Bartter / Nascimento Prematuro / Insuficiência Renal Crônica / Síndrome de Gitelman Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Newborn Idioma: En Ano de publicação: 2022 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 / Nascimento Prematuro / Insuficiência Renal Crônica / Síndrome de Gitelman Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Newborn Idioma: En Ano de publicação: 2022 Tipo de documento: Article