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Hematology / the Education Program of the American Society of Hematology. American Society of Hematology. Education Program, 2009, pp. 215 - 221
In recent years, there has been increasing interest in non-invasive iron measurement, especially of the liver and heart, in patients with iron overload. Serum... 
Liver - pathology | Myocardium - chemistry | Humans | Magnetic Resonance Imaging - methods | Liver - chemistry | Spleen - chemistry | Iron - analysis | Bone Marrow - chemistry | Ferritins - blood | Iron Overload - metabolism | Biopsy | Brain Chemistry | Pancreas - chemistry | Iron Overload - diagnosis | Pituitary Gland, Anterior - chemistry
Journal Article
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
Blood, ISSN 0006-4971, 11/2009, Volume 114, Issue 22, pp. 2021 - 2021
Abstract Abstract 2021 Poster Board I-1043 Therapeutic regimens that combine two chelators have the potential to improve iron excretion while avoiding... 
Journal Article
Blood, ISSN 0006-4971, 11/2009, Volume 114, Issue 22, pp. 4071 - 4071
Abstract Abstract 4071 Poster Board III-1006 Introduction Infection is the second most common cause of death in thalassemia. The innate immune system provides... 
Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 08/2019, Volume 127, Issue 4, pp. 355 - 360
To evaluate the impact of galsulfase enzyme replacement therapy (ERT) when initiated in adulthood for patients with mucopolysaccharidosis (MPS) VI. In 2005,... 
Adult | Mucopolysaccharidosis VI | Maroteaux-Lamy syndrome | Registry | Enzyme replacement therapy | Galsulfase | MEDICINE, RESEARCH & EXPERIMENTAL | WALK TEST | ENDURANCE | FOLLOW-UP | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | OUTCOMES | Heart | Enzymes | Glycosaminoglycans | Liver | Mucopolysaccharidosis | Adults | Ophthalmology | Health aspects | Pediatric neurology | Biopharmaceutics
Journal Article
Blood, ISSN 0006-4971, 11/2009, Volume 114, Issue 22, pp. 4069 - 4069
Abstract Abstract 4069 Poster Board III-1004 Introduction Transfused patients with β-thal major are known to experience clinical consequences of cardiac iron... 
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 12/2017, Volume 122, pp. 41 - 48
The mucopolysaccharidosis (MPS) disorders are ultra-rare lysosomal storage disorders associated with progressive accumulation of glycosaminoglycans (GAGs) in... 
Mucopolysaccharidosis | Diagnostic imaging | Neurological disease | Hydrocephalus | Surgery | Spinal cord compression | MEDICINE, RESEARCH & EXPERIMENTAL | MORQUIO-BRAILSFORD | IMAGING FINDINGS | IVA MORQUIO | CHILDREN | MAROTEAUX-LAMY-SYNDROME | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | NORMAL-PRESSURE HYDROCEPHALUS | SCORING SYSTEM | SPINAL-CORD COMPRESSION | OF-THE-LITERATURE | Brain - diagnostic imaging | Postoperative Complications - etiology | Humans | Postoperative Complications - prevention & control | Brain - enzymology | Lysosomes - enzymology | Mucopolysaccharidoses - etiology | Mucopolysaccharidoses - pathology | Brain - metabolism | Nerve Compression Syndromes - etiology | Lysosomes - metabolism | Glycosaminoglycans - toxicity | Hydrocephalus - diagnostic imaging | Mucopolysaccharidoses - complications | Spinal Cord Compression - diagnostic imaging | Intraoperative Neurophysiological Monitoring - methods | Neuroimaging - methods | Nerve Compression Syndromes - surgery | Neurosurgical Procedures - adverse effects | Brain - cytology | Congresses as Topic | Glycosaminoglycans - metabolism | Hydrocephalus - etiology | Spinal Cord Compression - surgery | Treatment Outcome | Spinal Cord Compression - etiology | Nerve Compression Syndromes - diagnostic imaging | Hydrocephalus - surgery | Neurosurgical Procedures - methods | Enzymes | Medical colleges | Brain damage | Nervous system diseases | Glycosaminoglycans
Journal Article
Journal Article
Journal Article