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Stroke, ISSN 0039-2499, 02/2013, Volume 44, Issue 2, pp. 340 - 349
Journal Article
Lancet, The, ISSN 0140-6736, 2008, Volume 372, Issue 9647, pp. 1427 - 1435
Summary Fabry's disease is an X-linked lysosomal storage disorder caused by abnormalities in the GLA gene, which leads to a deficiency in α-galactosidase A.... 
Internal Medicine | alpha-Galactosidase - genetics | alpha-Galactosidase - therapeutic use | Fabry Disease - epidemiology | Humans | Sex Factors | Fabry Disease - physiopathology | Female | Male | alpha-Galactosidase - metabolism | Fabry Disease - therapy | Fabry Disease - diagnosis | Care and treatment | Genetic aspects | Diagnosis | Fabry's disease | Risk factors
Journal Article
Stroke, ISSN 0039-2499, 01/2013, Volume 44, Issue 1, pp. 119 - 125
Journal Article
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 11/2001, Volume 38, Issue 11, pp. 769 - 775
Journal Article
Current Pharmaceutical Design, ISSN 1381-6128, 10/2013, Volume 19, Issue 33, pp. 6014 - 6030
Characteristic clinical manifestations of AFD such as acroparesthesias, angiokeratoma, corneal opacity, hypo/ and anhidrosis, gastrointestinal symptoms, renal... 
Anderson-Fabry disease | Stroke | Neurological complications | stroke | QUANTITATIVE-ANALYSIS | CRYPTOGENIC STROKE | CLINICAL MANIFESTATIONS | CEREBROVASCULAR COMPLICATIONS | SMALL FIBER DYSFUNCTION | ACUTE ISCHEMIC-STROKE | A-KNOCKOUT MOUSE | PHARMACOLOGY & PHARMACY | CEREBRAL-BLOOD-FLOW | ENZYME REPLACEMENT THERAPY | ALPHA-GALACTOSIDASE
Journal Article
Lancet, The, ISSN 0140-6736, 2012, Volume 379, Issue 9813, pp. 335 - 341
Journal Article