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Global reach of over 20 years of experience in the patient-centered Fabry Registry: Advancement of Fabry disease expertise and dissemination of real-world evidence to the Fabry community.
Wanner, Christoph; Ortiz, Alberto; Wilcox, William R; Hopkin, Robert J; Johnson, Jack; Ponce, Elvira; Ebels, Johan T; Batista, Julie L; Maski, Manish; Politei, Juan M; Martins, Ana Maria; Banikazemi, Maryam; Linhart, Ales; Mauer, Michael; Oliveira, João P; Weidemann, Frank; Germain, Dominique P.
Afiliação
  • Wanner C; Department of Medicine, Division of Nephrology, University Hospital of Würzburg, Würzburg, Germany. Electronic address: Wanner_C@ukw.de.
  • Ortiz A; Jiménez Díaz Foundation University Hospital and IIS-Fundación Jiménez Díaz UAM, Madrid, Spain; Department of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.
  • Wilcox WR; Division of Medical Genetics, Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.
  • Hopkin RJ; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, USA; Department of Pediatrics University of Cincinnati College of Medicine, Cincinnati, OH, USA.
  • Johnson J; Fabry Support & Information Group, Concordia, MO, USA.
  • Ponce E; Global Medical Affairs, Rare Nephrology, Sanofi, Cambridge, MA, USA.
  • Ebels JT; Global Medical Affairs, Rare Nephrology, Sanofi, Cambridge, MA, USA.
  • Batista JL; Epidemiology/Biostatistics, Sanofi, Cambridge, MA, USA.
  • Maski M; Global Medical Affairs, Rare Nephrology, Sanofi, Cambridge, MA, USA.
  • Politei JM; Foundation for the Study of Neurometabolic Diseases, FESEN, Buenos Aires, Argentina.
  • Martins AM; Reference Center for Inborn Errors of Metabolism, Federal University of São Paulo, São Paulo, Brazil.
  • Banikazemi M; Advanced Medical Genetics, Westchester Medical Center, Valhalla, NY, USA; New York Medical College and New York Health & Hospital, New York, NY, USA.
  • Linhart A; Department of Cardiovascular Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic; General University Hospital, Prague, Czech Republic.
  • Mauer M; Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, MN, USA.
  • Oliveira JP; Service of Human Genetics, São João University Hospital Centre; Unit of Genetics, Department of Pathology, Faculty of Medicine, University of Porto, Porto, Portugal.
  • Weidemann F; Department of Medicine I, Klinikum Vest GmbH, Knappschaftskrankenhaus Recklinghausen, Academic Teaching Hospital, Recklinghausen, Germany.
  • Germain DP; French Referral Center for Fabry disease and MetabERN European Reference Network for Inherited Metabolic Diseases, Division of Medical Genetics, University of Versailles, Paris-Saclay University, Montigny, France.
Mol Genet Metab ; 139(3): 107603, 2023 07.
Article em En | MEDLINE | ID: mdl-37236007
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Fabry Tipo de estudo: Observational_studies / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Fabry Tipo de estudo: Observational_studies / Prognostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article