X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (71) 71
humans (70) 70
male (51) 51
female (42) 42
muscular dystrophy (40) 40
sarcoglycanopathy (38) 38
child (37) 37
clinical neurology (35) 35
neurosciences (34) 34
sarcoglycans - genetics (31) 31
adult (29) 29
muscle, skeletal - pathology (29) 29
adolescent (26) 26
mutation (26) 26
child, preschool (24) 24
muscular dystrophies, limb-girdle - genetics (24) 24
mutations (23) 23
sarcoglycanopathies (21) 21
biopsy (20) 20
diagnosis (19) 19
sarcoglycanopathies - genetics (19) 19
gene (18) 18
phenotype (18) 18
middle aged (16) 16
muscle, skeletal - metabolism (16) 16
young adult (16) 16
deficiency (15) 15
dna mutational analysis (15) 15
immunohistochemistry (15) 15
neurology (15) 15
beta-sarcoglycan (14) 14
genetic aspects (14) 14
complex (13) 13
dystrophin (13) 13
genetics & heredity (13) 13
muscular dystrophies - genetics (13) 13
muscular dystrophies, limb-girdle - diagnosis (13) 13
muscular dystrophies, limb-girdle - pathology (13) 13
girdle muscular-dystrophy (12) 12
limb-girdle muscular dystrophy (12) 12
proteins (12) 12
research (12) 12
analysis (11) 11
mutation - genetics (11) 11
sarcoglycanopathies - diagnosis (11) 11
sarcoglycanopathies - pathology (10) 10
care and treatment (9) 9
genotype (9) 9
sarcoglycans - metabolism (9) 9
dystrophy (8) 8
gamma-sarcoglycan (8) 8
genetic testing (8) 8
infant (8) 8
limb girdle muscular dystrophy (8) 8
myopathy (8) 8
patients (8) 8
sarcoglycanopathies - metabolism (8) 8
spectrum (8) 8
cytoskeletal proteins - genetics (7) 7
dystrophin - genetics (7) 7
muscular dystrophies - diagnosis (7) 7
myoglobinuria (7) 7
sarcoglycan (7) 7
sgca (7) 7
animals (6) 6
calpainopathy (6) 6
cardiomyopathy (6) 6
diagnosis, differential (6) 6
duchenne (6) 6
exons - genetics (6) 6
gamma-sarcoglycanopathy (6) 6
gene mutations (6) 6
genes (6) 6
glycoprotein complex (6) 6
homozygote (6) 6
membrane glycoproteins - genetics (6) 6
missense mutations (6) 6
muscles (6) 6
muscular dystrophies - pathology (6) 6
musculoskeletal diseases (6) 6
pedigree (6) 6
retrospective studies (6) 6
skeletal-muscle (6) 6
alpha-sarcoglycan gene (5) 5
biomedicine (5) 5
delta-sarcoglycan (5) 5
disease (5) 5
duchenne muscular dystrophy (5) 5
dysferlin (5) 5
dysferlinopathy (5) 5
dystrophinopathy (5) 5
exercise intolerance (5) 5
family health (5) 5
founder mutation (5) 5
gene expression (5) 5
genetic research (5) 5
heart (5) 5
india (5) 5
involvement (5) 5
magnetic resonance imaging (5) 5
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Molecular Therapy, ISSN 1525-0016, 04/2017, Volume 25, Issue 4, pp. 855 - 869
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 07/2005, Volume 26, Issue 1, pp. 59 - 59
Journal Article
Journal Article
Indian Journal of Medical Research, ISSN 0971-5916, 06/2012, Volume 135, Issue 6, pp. 878 - 886
Background & objectives: Calpain-3, a Ca2+-dependent protease has been implicated in the pathology of neuromuscular disorders (NMDs). The current study aimed... 
Western blot | Calpain | Limb girdle muscular dystrophy | Neuromuscular disorders | Muscular dystrophy | MEDICINE, RESEARCH & EXPERIMENTAL | neuromuscular disorders | IMMUNOLOGY | limb girdle muscular dystrophy | western blot | MDX MICE | SKELETAL-MUSCLE | MEDICINE, GENERAL & INTERNAL | muscular dystrophy | IN-VITRO | NECROSIS | GENE | MUTATIONS | EXPRESSION | LGMD2A | DYSFERLINOPATHIES | Calpain - metabolism | Gene Expression - genetics | Humans | Middle Aged | Sarcoglycanopathies - pathology | Child, Preschool | Infant | Male | Calpain - genetics | Muscle Proteins - metabolism | Adult | Female | Muscular Dystrophies, Limb-Girdle - pathology | Child | Muscular Dystrophies, Limb-Girdle - diagnosis | Muscular Dystrophy, Duchenne - pathology | India | Muscle Proteins - genetics | Muscular Dystrophies, Limb-Girdle - metabolism | Sarcoglycanopathies - diagnosis | Sarcoglycanopathies - metabolism | Adolescent | Muscular Dystrophy, Duchenne - metabolism | Muscle, Skeletal | Muscular Dystrophy, Duchenne - diagnosis | Physiology, Pathological | Physiological aspects | Development and progression | Muscle diseases | Research | Health aspects | Proteins | Signal transduction | Musculoskeletal system | Immunoglobulins | Scholarships & fellowships | Biopsy | Mutation | Gene expression | Kinases | Quantitative analysis | Index Medicus | Original
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2016, Volume 11, Issue 4, pp. e0153095 - e0153095
Journal Article
Journal Article