X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (654) 654
Publication (73) 73
Book / eBook (47) 47
Book Chapter (23) 23
Book Review (19) 19
Newspaper Article (18) 18
Magazine Article (3) 3
Newsletter (2) 2
Reference (2) 2
Conference Proceeding (1) 1
Dissertation (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (568) 568
index medicus (318) 318
male (309) 309
female (285) 285
muscular dystrophy (256) 256
adult (242) 242
clinical neurology (233) 233
middle aged (192) 192
neurosciences (153) 153
adolescent (149) 149
child (116) 116
aged (105) 105
muscular dystrophy, facioscapulohumeral - complications (103) 103
diagnosis (93) 93
muscular dystrophies - complications (91) 91
neurology (91) 91
facioscapulohumeral muscular dystrophy (87) 87
disease (81) 81
young adult (73) 73
care and treatment (68) 68
myopathy (63) 63
animals (62) 62
muscular dystrophies - genetics (62) 62
muscles (61) 61
muscular dystrophy, facioscapulohumeral - genetics (61) 61
duchenne muscular-dystrophy (59) 59
muscle, skeletal - pathology (59) 59
mutation (59) 59
muscular-dystrophy (58) 58
neuromuscular diseases (57) 57
fshd (56) 56
pediatrics (56) 56
phenotype (56) 56
research (54) 54
child, preschool (52) 52
biopsy (51) 51
myotonic-dystrophy (51) 51
facioscapulohumeral muscular-dystrophy (50) 50
medicine & public health (49) 49
muscular dystrophy, facioscapulohumeral - physiopathology (49) 49
duchenne muscular dystrophy (46) 46
muscular dystrophy, facioscapulohumeral - diagnosis (46) 46
retrospective studies (46) 46
surgery (46) 46
myotonic dystrophy (45) 45
analysis (44) 44
diseases (43) 43
neuromuscular disease (43) 43
article (42) 42
genetic aspects (41) 41
genetics (40) 40
muscular diseases (40) 40
skeletal-muscle (40) 40
children (39) 39
gene (39) 39
muscle, skeletal - physiopathology (39) 39
infant (38) 38
musculoskeletal system (38) 38
muscular dystrophies - physiopathology (37) 37
orthopedics (37) 37
risk factors (37) 37
severity of illness index (36) 36
dystrophy (35) 35
quality of life (35) 35
muscle (34) 34
muscular dystrophies - diagnosis (34) 34
neuromuscular disorders (34) 34
patients (34) 34
rehabilitation (34) 34
cardiomyopathy (33) 33
diagnosis, differential (33) 33
disease progression (33) 33
electromyography (33) 33
facioscapulohumeral dystrophy (33) 33
health aspects (33) 33
muscular dystrophies (33) 33
muscular dystrophies - pathology (33) 33
musculoskeletal diseases (33) 33
genetics & heredity (32) 32
magnetic resonance imaging (31) 31
muscular dystrophy, facioscapulohumeral - pathology (31) 31
neuromuscular diseases - complications (31) 31
pathology (31) 31
proteins (31) 31
medical research (30) 30
medicine, general & internal (29) 29
management (28) 28
medicine (28) 28
review (27) 27
scapula - surgery (27) 27
shoulder (27) 27
electrocardiography (26) 26
follow-up studies (26) 26
myotonic dystrophy - complications (26) 26
pedigree (26) 26
treatment outcome (26) 26
cross-sectional studies (25) 25
mutations (25) 25
complications and side effects (24) 24
neuromuscular diseases - physiopathology (24) 24
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (39) 39
Holland Bloorview Kids Rehabilitation - Stacks (6) 6
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Humber River Regional Hospital - Church Stacks (1) 1
Mt Sinai Hospital - Pathology (1) 1
Sunnybrook Health Sciences Centre - Holland Reference (1) 1
Toronto East General Hospital - Stacks (1) 1
UTL at Downsview - May be requested (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neurology, ISSN 0028-3878, 07/2016, Volume 87, Issue 4, pp. e39 - e39
A 21-year-old Brazilian woman presented with mild facial muscle weakness, scapular winging and an asymmetric shoulder girdle, and peroneal weakness. Medical... 
CLINICAL NEUROLOGY | Young Adult | Muscular Dystrophy, Facioscapulohumeral - complications | Retinal Telangiectasis - etiology | Female | Humans
Journal Article
Chinese medical journal, ISSN 0366-6999, 09/2018, Volume 131, Issue 18, p. 2164
Facioscapulohumeral muscular dystrophy (FSHD) is characterized by asymmetric muscular deficit of facial, shoulder-girdle muscles, and descending to lower limb... 
Muscular Dystrophy, Facioscapulohumeral - complications | Humans | Evoked Potentials, Visual | Adult | Male | Muscle, Skeletal | Peripheral Nervous System Diseases - complications | Child | Epilepsies, Myoclonic - complications
Journal Article
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 4/2011, Volume 31, Issue 2, pp. 155 - 166
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 09/2018, Volume 22, Issue 5, pp. 782 - 785
To assess the long-term natural course of early-onset facioscapulohumeral dystrophy (FSHD), which is important for patient management and trial-readiness, and... 
Infantile FSHD | Facioscapulohumeral dystrophy | Early-onset FSHD | Neuromuscular disorders | Natural history | DIAGNOSIS | MUSCULAR-DYSTROPHY | PHENOTYPE | PEDIATRICS | CLINICAL NEUROLOGY | Muscular Dystrophy, Facioscapulohumeral - complications | Phenotype | Follow-Up Studies | Humans | Middle Aged | Adolescent | Age of Onset | Adult | Female | Male
Journal Article
Journal Article