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Consensus recommendations for diagnosis, management and treatment of Fabry disease in paediatric patients.
Germain, Dominique P; Fouilhoux, Alain; Decramer, Stéphane; Tardieu, Marine; Pillet, Pascal; Fila, Marc; Rivera, Serge; Deschênes, Georges; Lacombe, Didier.
Afiliación
  • Germain DP; Division of Medical Genetics, University of Versailles, Montigny, France.
  • Fouilhoux A; Metabolic Diseases Unit, HFME University Hospital Lyon, Lyon, France.
  • Decramer S; Paediatric Department, Inserm U1048, Toulouse University Hospital, Toulouse, France.
  • Tardieu M; Paediatric Department, Tours University Hospital, Toulouse, France.
  • Pillet P; Paediatric Department, Bordeaux University Hospital Pellegrin, Bordeaux, France.
  • Fila M; Department of Paediatric Nephrology-Montpellier University, Arnaud de Villeneuve Hospital, Montpellier, France.
  • Rivera S; Department of Paediatric Neurology, Bayonne Hospital, Bayonne, France.
  • Deschênes G; Department of Paediatric Nephrology, Paris University Hospital Robert Debré, Paris, France.
  • Lacombe D; Department of Medical Genetics, CHU Bordeaux INSERM U1211, Université de Bordeaux, Bordeaux, France.
Clin Genet ; 96(2): 107-117, 2019 08.
Article en En | MEDLINE | ID: mdl-30941742

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Fabry / Guías de Práctica Clínica como Asunto / Consenso Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Límite: Child / Child, preschool / Humans Idioma: En Revista: Clin Genet Año: 2019 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Fabry / Guías de Práctica Clínica como Asunto / Consenso Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Límite: Child / Child, preschool / Humans Idioma: En Revista: Clin Genet Año: 2019 Tipo del documento: Article País de afiliación: Francia