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Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 12/2011, Volume 34, Issue 6, pp. 1183 - 1197
The mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders caused by the absence of functional enzymes that contribute to the degradation of... 
Biochemistry, general | Human Genetics | Pediatrics | Internal Medicine | Medicine & Public Health | Metabolic Diseases | MEDICINE, RESEARCH & EXPERIMENTAL | BONE-MARROW-TRANSPLANTATION | VALVULAR HEART-DISEASE | LEFT-VENTRICULAR ANEURYSM | N-ACETYLGALACTOSAMINE 4-SULFATASE | ENZYME-REPLACEMENT THERAPY | MAROTEAUX-LAMY-SYNDROME | HUNTER OUTCOME SURVEY | MITRAL-VALVE-REPLACEMENT | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | L-IDURONIDASE LARONIDASE | CORONARY-ARTERY-DISEASE | Humans | Middle Aged | Hypertrophy, Left Ventricular - diagnosis | Child, Preschool | Mucopolysaccharidoses - therapy | Male | Mitral Valve Insufficiency - epidemiology | Hypertrophy, Left Ventricular - epidemiology | Mucopolysaccharidoses - epidemiology | Mucopolysaccharidoses - classification | Aortic Valve Stenosis - epidemiology | Heart Valve Diseases - epidemiology | Electrocardiography | Adult | Female | Heart Valve Diseases - diagnosis | Tachycardia, Sinus - epidemiology | Tachycardia, Sinus - diagnosis | Child | Echocardiography | Comorbidity | Glycosaminoglycans - metabolism | Aortic Valve Stenosis - diagnosis | Mitral Valve Insufficiency - diagnosis | Coronary Artery Disease - diagnosis | Adolescent | Age of Onset | Coronary Artery Disease - epidemiology | Causality | Enzymes | Medical colleges | Glycosaminoglycans | Development and progression | Mucopolysaccharidosis | Transplantation | Hematopoietic stem cells | Cardiac patients | Electrocardiogram | Medical genetics | Diagnosis | Children | Cardiology | Cardiovascular diseases | Health aspects | Review
Journal Article
British Journal of Clinical Pharmacology, ISSN 0306-5251, 02/2013, Volume 75, Issue 2, pp. 450 - 462
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