X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (329) 329
Publication (39) 39
Book Chapter (2) 2
Newspaper Article (2) 2
Book / eBook (1) 1
Book Review (1) 1
Conference Proceeding (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (144) 144
female (96) 96
male (94) 94
index medicus (91) 91
child (76) 76
adolescent (75) 75
adult (74) 74
genetics & heredity (52) 52
enzyme replacement therapy (51) 51
child, preschool (46) 46
mucopolysaccharidosis (43) 43
enzymes (42) 42
pediatrics (40) 40
children (38) 38
hematology (35) 35
medicine, research & experimental (35) 35
endocrinology & metabolism (33) 33
disease (30) 30
young adult (30) 30
middle aged (29) 29
treatment outcome (25) 25
article (24) 24
genetics (23) 23
care and treatment (22) 22
maroteaux-lamy-syndrome (21) 21
medical research (20) 20
diagnosis (19) 19
infant (19) 19
safety (19) 19
thalassemia (19) 19
double-blind method (18) 18
enzyme-replacement therapy (18) 18
iron - metabolism (18) 18
medicine, experimental (18) 18
beta-thalassemia (17) 17
efficacy (17) 17
glycosaminoglycans (17) 17
health aspects (17) 17
iron overload (17) 17
bone-marrow-transplantation (16) 16
endurance (16) 16
liver - metabolism (16) 16
medicine & public health (15) 15
animals (14) 14
clinical trials (14) 14
iron overload - etiology (14) 14
medicine (14) 14
sulfates (14) 14
analysis (13) 13
anemia, sickle cell - therapy (13) 13
biopharmaceutics (13) 13
mucopolysaccharidosis vi (13) 13
n-acetylgalactosamine 4-sulfatase (13) 13
internal medicine (12) 12
management (12) 12
patients (12) 12
recombinant proteins - therapeutic use (12) 12
endocrinology (11) 11
growth (11) 11
magnetic resonance imaging (11) 11
maroteaux-lamy syndrome (11) 11
molecular biology (11) 11
n-acetylgalactosamine-4-sulfatase - therapeutic use (11) 11
original (11) 11
transplantation (11) 11
biochemistry (10) 10
congenital, hereditary, and neonatal diseases and abnormalities (10) 10
elosulfase alfa (10) 10
endocrinology, diabetes and metabolism (10) 10
ferritins - blood (10) 10
follow-up studies (10) 10
iron chelating agents - therapeutic use (10) 10
iron overload - metabolism (10) 10
liver - pathology (10) 10
mucopolysaccharidosis iv - drug therapy (10) 10
mucopolysaccharidosis vi - drug therapy (10) 10
phenotype (10) 10
quality of life (10) 10
age factors (9) 9
aged (9) 9
biochemistry, general (9) 9
development and progression (9) 9
disease progression (9) 9
enzyme replacement therapy - methods (9) 9
human genetics (9) 9
inflammation (9) 9
iron (9) 9
iron - analysis (9) 9
medical genetics (9) 9
metabolic diseases (9) 9
mps vi (9) 9
original article (9) 9
oxidative stress (9) 9
pharmacology & pharmacy (9) 9
research (9) 9
sickle cell disease (9) 9
transfusion reaction (9) 9
beta-thalassemia - metabolism (8) 8
beta-thalassemia - therapy (8) 8
biochemistry & molecular biology (8) 8
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Molecular Genetics and Metabolism, ISSN 1096-7192, 2012, Volume 105, Issue 2, pp. S33 - S33
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S91 - S91
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 05/2019, Volume 14, Issue 1, pp. 118 - 21
Journal Article
ORPHANET JOURNAL OF RARE DISEASES, ISSN 1750-1172, 06/2019, Volume 14, Issue 1, pp. 137 - 25
Journal Article
Journal Article
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