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Is autosomal dominant polycystic kidney disease an early sweet disease?
Dachy, Angélique; Decuypere, Jean-Paul; Vennekens, Rudi; Jouret, François; Mekahli, Djalila.
Afiliação
  • Dachy A; PKD Research Group, GPURE, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Decuypere JP; Department of Pediatrics, ULiège Academic Hospital, Liège, Belgium.
  • Vennekens R; Laboratory of Translational Research in Nephrology (LTRN), GIGA Cardiovascular Sciences, ULiège, Liège, Belgium.
  • Jouret F; PKD Research Group, GPURE, Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
  • Mekahli D; Laboratory of Ion Channel Research, Department of Cellular and Molecular Medicine, VIB Center for Brain and Disease Research, KU Leuven, Leuven, Belgium.
Pediatr Nephrol ; 37(9): 1945-1955, 2022 09.
Article em En | MEDLINE | ID: mdl-34988697
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Limite: Adult / Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Limite: Adult / Child / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article