Your browser doesn't support javascript.
loading
Bi-allelic REN Mutations and Undetectable Plasma Renin Activity in a Patient With Progressive CKD.
Jorge, Sofia; Kidd, Kendrah; Vylet'al, Petr; Nogueira, Estela; Martin, Lauren; Howard, Katrice; Baresová, Veronika; Hodanová, Katerina; Hnízda, Ales; Moldovan, Oana; Silveira, Catarina; Coutinho, Ana Margarida; Lopes, José António; Bleyer, Anthony J; Kmoch, Stanislav; Zivná, Martina.
Afiliação
  • Jorge S; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.
  • Kidd K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.
  • Vylet'al P; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Nogueira E; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.
  • Martin L; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.
  • Howard K; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Baresová V; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
  • Hodanová K; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.
  • Hnízda A; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.
  • Moldovan O; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.
  • Silveira C; Genetic Department of Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.
  • Coutinho AM; GenoMed - Diagnósticos de Medicina Molecular, S.A., Lisbon, Portugal.
  • Lopes JA; GenoMed - Diagnósticos de Medicina Molecular, S.A., Lisbon, Portugal.
  • Bleyer AJ; Department of Nephrology and Renal Transplant, Hospital de Santa Maria, CHULN, EPE, Lisbon, Portugal.
  • Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic.
  • Zivná M; Section on Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Kidney Int Rep ; 8(5): 1112-1116, 2023 May.
Article em En | MEDLINE | ID: mdl-37180515
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article