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Genetics and Molecular Biology, ISSN 1415-4757, 2010, Volume 33, Issue 4, pp. 589 - 604
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 05/2013, Volume 109, Issue 1, pp. 62 - 69
Journal Article
Pharmacoepidemiology and drug safety, ISSN 1053-8569, 2012, Volume 21, Issue 7, pp. 749 - 752
Purpose The Mucopolysaccharidosis Type I (MPS I) Registry is an international observational database that tracks the natural history and the outcomes of... 
laronidase | enzyme replacement therapy | Registry | MPS I | source document verification | Laronidase | Enzyme replacement therapy | Source document verification | PHARMACOLOGY & PHARMACY | Enzymes | Databases | Epidemiology | Metabolic disorders
Journal Article
Journal Article
Arquivos de Neuro-Psiquiatria, ISSN 0004-282X, 12/1996, Volume 54, Issue 4, pp. 655 - 660
O angioma cavernoso ou cavemoma é malformação vascular que acomete 0,5 a 0,7% da população, perfazendo 8 a 15% de todas as malformações vasculares do... 
Familial malformation | Cavernous malformation | Cerebrovascular malformation | Hereditary disorder | Cavernous angioma | PSYCHIATRY | NEUROSCIENCES
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 05/2013, Volume 109, Issue 1, pp. 62 - 69
Background: Mucopolysaccharidosis type VI (MPS VI) is a progressive, chronic and multisystem lysosomal storage disease with a wide disease spectrum. Clinical... 
Journal Article
Arquivos de Neuro-Psiquiatria, ISSN 0004-282X, 12/1996, Volume 54, Issue 4, pp. 655 - 660
O angioma cavernoso ou cavemoma é malformação vascular que acomete 0,5 a 0,7% da população, perfazendo 8 a 15% de todas as malformações vasculares do... 
forma familiar | cerebrovascular malformation | familial malformation | hereditary disorder | angioma cavernoso | cavernous malformation | cavernous angioma | cavemoma | malformação vascular cerebral | doença genética
Journal Article
Arquivos de Neuro-Psiquiatria, ISSN 0004-282X, 12/1996, Volume 54, Issue 4, pp. 655 - 660
O angioma cavernoso ou cavemoma é malformação vascular que acomete 0,5 a 0,7% da população, perfazendo 8 a 15% de todas as malformações vasculares do... 
Journal Article
Revista da Associacao Medica Brasileira (1992), 05/2010, Volume 56, Issue 3, p. 271
Mucopolysaccharidoses (MPS) are rare genetic diseases caused by deficiency of specific lysosomal enzymes that affect catabolism of glycosaminoglycans (GAG).... 
Enzyme Replacement Therapy - methods | Humans | Brazil | Enzyme Replacement Therapy - utilization | Mucopolysaccharidoses - classification | Mucopolysaccharidoses - drug therapy | Practice Guidelines as Topic
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2013, Volume 8, Issue 12, p. e83466
Journal Article
Magazine Article