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  • Marieke Biegstraaten, Reynir Arngrímsson, +31 authors Carla E. M. Hollak
  • Medicine, Biology
  • Orphanet Journal of Rare Diseases
  • 2015 (First Publication: 27 March 2015)
  • IntroductionFabry disease (FD) is a lysosomal storage disorder resulting in progressive nervous system, kidney and heart disease. Enzyme replacement therapy (ERT) may halt or attenuate diseaseExpand
  • Frédéric Barbey, Noureddine Brakch, +8 authors Daniel Hayoz
  • Medicine
  • Arteriosclerosis, thrombosis, and vascular…
  • 2006 (First Publication: 1 April 2006)
  • Objectives—Fabry disease is an X-linked disorder resulting from α-galactosidase A deficiency. The cardiovascular findings include left ventricular hypertrophy (LVH) and increased intima-mediaExpand
  • Frédéric Barbey, Noureddine Brakch, +5 authors Daniel Hayoz
  • Medicine
  • Acta paediatrica (Oslo, Norway : ). Supplement
  • 2006 (First Publication: 1 April 2006)
  • AIM Fabry disease is considered primarily as a progressive small vessel disease, with ischaemic degenerative lesions involving the kidneys, brain and heart. Macrovascular involvement in male patientsExpand