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Antenatal Membranous Nephropathy and Type 2 (Axonal) Charcot-Marie-Tooth With Mutations in the Metallo-Membrane Endopeptidase Gene: A Call for Family Screening and Pharmacovigilance.
Nortier, Joëlle L; Remiche, Gauthier; Delrée, Paul; Nauta, Jeroen; Notermans, Nicolette C; Vivarelli, Marina; Diodato, Daria; Solé, Guilhem; Debiec, Hanna; Ronco, Pierre.
Afiliação
  • Nortier JL; Nephrology Department, CHU Brugmann, Université libre de Bruxelles, Brussels, Belgium.
  • Remiche G; Neurology Department, Centre de Référence Neuromusculaire Erasme-HUDERF, Hôpital Erasme, Université libre de Bruxelles, Brussels, Belgium.
  • Delrée P; Pathology Department, Institute of Pathology and Genetics, Gosselies, Belgium.
  • Nauta J; Department of Pediatric Nephrology, Erasmus MC, Sophia Childrens Hospital, Rotterdam, The Netherlands.
  • Notermans NC; Department of Neurology, University Medical Center, Utrecht, The Netherlands.
  • Vivarelli M; U.O. Nefrologia e Dialisi, Children's Hospital Bambino Gesù, IRCCS, Roma, Italy.
  • Diodato D; Neuromuscular and Neurodegenerative Diseases Unit, Children Research, Children's Hospital Bambino Gesù, IRCCS, Roma, Italy.
  • Solé G; Centre de référence des maladies neuromusculaires AOC, Pellegrin Hospital, Bordeaux, France.
  • Debiec H; Sorbonne Université, Inserm UMR_S1155, Tenon Hospital, Paris, France.
  • Ronco P; Sorbonne Université, Inserm UMR_S1155, Tenon Hospital, Paris, France.
Kidney Int Rep ; 6(7): 1981-1986, 2021 Jul.
Article em En | MEDLINE | ID: mdl-34307994

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article