X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (301) 301
index medicus (247) 247
male (185) 185
female (168) 168
glycogen (140) 140
adult (111) 111
middle aged (84) 84
animals (80) 80
neurosciences (74) 74
enzyme replacement therapy (69) 69
clinical neurology (64) 64
infant (63) 63
enzymes (61) 61
mutation (58) 58
pompe disease (56) 56
child (55) 55
diagnosis (55) 55
genetics & heredity (55) 55
glycogen storage disease type ii - complications (54) 54
glycogen - metabolism (50) 50
glycogen storage disease type ii - diagnosis (49) 49
adolescent (48) 48
pediatrics (47) 47
endocrinology & metabolism (45) 45
aged (44) 44
child, preschool (44) 44
glycogen storage disease type ii - pathology (44) 44
acid maltase deficiency (43) 43
medicine, research & experimental (43) 43
glycogen storage disease type ii - diagnostic imaging (41) 41
mice (41) 41
magnetic resonance imaging (40) 40
medicine (40) 40
medicine & public health (40) 40
muscle, skeletal - metabolism (40) 40
muscles (40) 40
physiological aspects (39) 39
metabolism (38) 38
young adult (38) 38
infant, newborn (37) 37
muscle, skeletal - pathology (37) 37
biopsy (34) 34
children (34) 34
glucose (34) 34
liver (34) 34
disease (33) 33
glucose metabolism (33) 33
glycogenosis (33) 33
phenotype (33) 33
diagnostic imaging (32) 32
glycogen storage disease type ii - genetics (32) 32
health aspects (32) 32
medical research (32) 32
acid alpha-glucosidase (31) 31
analysis (31) 31
glycogen-storage-disease (30) 30
research (30) 30
neurology (28) 28
pathology (28) 28
proteins (28) 28
age of onset (27) 27
echocardiography (27) 27
glycogen storage disease type ii - physiopathology (27) 27
internal medicine (27) 27
patients (27) 27
research article (27) 27
skeletal-muscle (27) 27
alpha-glucosidases - genetics (26) 26
amylases (26) 26
genetic aspects (26) 26
glycogen storage disease type ii - drug therapy (26) 26
glycogen storage disease type ii - therapy (26) 26
physiology (26) 26
electrocardiography (25) 25
medicine, experimental (25) 25
radiography (25) 25
cardiac & cardiovascular systems (24) 24
diagnosis, differential (24) 24
rodents (24) 24
science (24) 24
ultrasonography (24) 24
alpha-glucosidases - therapeutic use (23) 23
cell biology (23) 23
insulin (23) 23
multidisciplinary sciences (23) 23
article (22) 22
care and treatment (22) 22
glucose - metabolism (22) 22
musculoskeletal system (22) 22
risk factors (22) 22
synthesis (22) 22
cardiomyopathy (21) 21
glycogen storage disease - complications (21) 21
metabolic diseases (21) 21
abridged index medicus (20) 20
alglucosidase alpha (20) 20
biochemistry (20) 20
biochemistry, general (20) 20
disease models, animal (20) 20
glycogen storage disease type ii (20) 20
more...
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, 02/2018, Volume 123, Issue 2, pp. 85 - 91
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2018, Volume 72, Issue 20, pp. 2485 - 2506
Hereditary muscular diseases commonly involve the heart. Cardiac manifestations encompass a spectrum of phenotypes, including both cardiomyopathies and rhythm... 
arrhythmias | dystrophy | skeletal muscle | myopathy | cardiomyopathies | CARDIAC & CARDIOVASCULAR SYSTEMS | RESTRICTIVE CARDIOMYOPATHY | FRIEDREICHS-ATAXIA | CLINICAL SPECTRUM | BARTH-SYNDROME | LINKED DILATED CARDIOMYOPATHY | LIMB-GIRDLE | LEFT-VENTRICULAR NONCOMPACTION | DIAGNOSTIC WORK-UP | HYPERTROPHIC CARDIOMYOPATHY | DUCHENNE MUSCULAR-DYSTROPHY | Glycogen Storage Disease Type II - genetics | Muscular Diseases - epidemiology | Humans | Muscular Dystrophy, Duchenne - epidemiology | Glycogen Storage Disease Type II - diagnostic imaging | Muscular Dystrophies - genetics | Muscular Dystrophy, Duchenne - diagnostic imaging | Phenotype | Heart Diseases - epidemiology | Muscular Dystrophies - epidemiology | Pedigree | Review Literature as Topic | Glycogen Storage Disease Type II - epidemiology | Heart Diseases - diagnostic imaging | Muscular Diseases - genetics | Muscular Dystrophies - diagnostic imaging | Muscular Dystrophy, Duchenne - genetics | Heart Diseases - genetics | Muscular Diseases - diagnostic imaging | Heart | Arrhythmia | Creatine kinase | Glycogen | Muscles | Genetic aspects | Lactic acid | Cardiology | Creatine | Fatty acids | Genetic screening | Pediatrics | Conduction | Cardiac arrhythmia | Disease | Muscular diseases | Cardiomyopathy | Disorders | Kinases | Muscular dystrophy | Defects | Eutrophication | Genotype & phenotype | Mitochondria | Glycogenosis | Ataxia | Oxidation | Bioindicators | Heart diseases | Age | Heart failure | Phenotypes | Neuromuscular diseases | Genetic disorders | Cardiac muscle | Patients | Coronary artery disease | Skeletal muscle | Diseases | Storage diseases | Friedreich's ataxia | Musculoskeletal system | Medical prognosis | Family studies | Biomarkers | Ventricle | Mutation
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2016, Volume 11, Issue 10, p. e0163493
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2016, Volume 11, Issue 7, p. e0158912
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 09/2016, Volume 119, Issue 1-2, pp. 115 - 123
Journal Article
Journal of Neurology, ISSN 0340-5354, 10/2017, Volume 264, Issue 10, pp. 2110 - 2118
Journal Article
Neurology, ISSN 0028-3878, 06/2016, Volume 86, Issue 24, pp. e250 - e251
Journal Article
Journal Article