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Risk factors for severe clinical events in male and female patients with Fabry disease treated with agalsidase beta enzyme replacement therapy: Data from the Fabry Registry.
Hopkin, Robert J; Cabrera, Gustavo; Charrow, Joel; Lemay, Roberta; Martins, Ana Maria; Mauer, Michael; Ortiz, Alberto; Patel, Manesh R; Sims, Katherine; Waldek, Stephen; Warnock, David G; Wilcox, William R.
Afiliación
  • Hopkin RJ; Cincinnati Children's Hospital Medical Center, Cincinnati, USA; Department of Pediatrics, University of Cincinnati College Medicine, Cincinnati, USA. Electronic address: rob.hopkin@cchmc.org.
  • Cabrera G; Centro Cardiovascular Bolivar, Buenos Aires, Argentina. Electronic address: gustavo.h.cabrera@hotmail.com.
  • Charrow J; Division of Genetics, Birth Defects and Metabolism, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, USA. Electronic address: jcharrow@northwestern.edu.
  • Lemay R; Strategic Epidemiology & Biostatistics, Rare Diseases, Sanofi Genzyme, Cambridge, USA. Electronic address: Roberta.Lemay@genzyme.com.
  • Martins AM; Reference Center for Inborn Errors of Metabolism, Federal University of São Paulo, São Paulo, Brazil. Electronic address: martins.anamaria@uol.com.br.
  • Mauer M; Departments of Pediatrics and Medicine, University of Minnesota, Minneapolis, USA. Electronic address: mauer002@umn.edu.
  • Ortiz A; Unidad de Dialisis, IIS-Fundacion Jimenez Diaz, School of Medicine, UAM, IRSIN, REDINREN, Madrid, Spain. Electronic address: AOrtiz@fjd.es.
  • Patel MR; Division of Cardiovascular Medicine, Duke University School of Medicine, Durham, USA. Electronic address: patel017@mc.duke.edu.
  • Sims K; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, USA. Electronic address: Sims@Helix.MGH.Harvard.edu.
  • Waldek S; University of Sunderland, Sunderland, United Kingdom. Electronic address: stephen.waldek@sunderland.ac.uk.
  • Warnock DG; Division of Nephrology, University of Alabama at Birmingham, Birmingham, USA. Electronic address: dwarnock@uab.edu.
  • Wilcox WR; Division of Medical Genetics, Department of Human Genetics, Emory University School of Medicine, Atlanta, USA. Electronic address: william.wilcox@emory.edu.
Mol Genet Metab ; 119(1-2): 151-9, 2016 09.
Article en En | MEDLINE | ID: mdl-27510433
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Fabry / Alfa-Galactosidasa / Accidente Cerebrovascular / Isoenzimas / Enfermedades Renales Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies Límite: Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2016 Tipo del documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Fabry / Alfa-Galactosidasa / Accidente Cerebrovascular / Isoenzimas / Enfermedades Renales Tipo de estudio: Clinical_trials / Etiology_studies / Risk_factors_studies Límite: Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2016 Tipo del documento: Article