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Journal of Clinical Neuroscience, ISSN 0967-5868, 07/2019, Volume 65, pp. 83 - 86
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 2013, Volume 36, Issue 2, pp. 247 - 255
Journal Article
Journal of Clinical Neuroscience, ISSN 0967-5868, 07/2019, Volume 65, pp. 83 - 86
Back ground and objective: Fabry's disease, is the most prevalent lysosomal storage disorder and is notorious for its early multi-organ involvement leading to... 
Stroke | Stroke prevention | Enzyme replacement therapy | Fabry's disease | Meta-analysis | EFFICACY | SAFETY | ALPHA | OUTCOMES | NEUROSCIENCES | CLINICAL NEUROLOGY | AGALSIDASE-BETA | Stroke (Disease) | Prevention | Enzymes | Health aspects | Analysis | Biopharmaceutics
Journal Article
Journal Article
Journal Article
Journal Article
Journal Article
Respirology Case Reports, ISSN 2051-3380, 12/2015, Volume 3, Issue 4, pp. 159 - 161
A dult P ompe disease/acid maltase deficiency is an autosomal recessive disorder resulting in accumulation of glycogen in skeletal muscles, leading to myopathy... 
P | A | ompe disease | enzyme replacement therapy | non‐invasive ventilation | dult | ome | V | entilation | H | M | echanical | Adult Pompe disease | Home Mechanical Ventilation | Enzyme replacement therapy | Non-invasive ventilation | Enzymes
Journal Article
Bone, ISSN 8756-3282, 2009, Volume 44, pp. S52 - S52
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 07/2019
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2011, Volume 21, Issue 9, pp. 701 - 701
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 04/2019, Volume 126, Issue 4, pp. 448 - 459
Fabry disease is a rare X-linked inherited multisystem disorder resulting from deficiency of the lysosomal enzyme alpha-galactosidase A. Currently, specific... 
Fabry disease | Agalsidase alfa | Enzyme replacement therapy (ERT) | Post-marketing surveillance
Journal Article