X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (38) 38
index medicus (34) 34
clinical neurology (29) 29
male (26) 26
neurosciences (24) 24
child (23) 23
female (20) 20
spinal muscular atrophy (17) 17
neurology (16) 16
adolescent (15) 15
child, preschool (15) 15
children (14) 14
adult (12) 12
pediatrics (11) 11
duchenne muscular dystrophy (10) 10
functional motor scale (9) 9
outcome measures (9) 9
severity of illness index (9) 9
research (8) 8
walking (8) 8
young adult (7) 7
analysis (6) 6
clinical trials (6) 6
middle aged (6) 6
muscular dystrophy (6) 6
reliability (6) 6
treatment outcome (6) 6
6-minute walk test (5) 5
article (5) 5
atrophy (5) 5
dystrophy (5) 5
muscular dystrophy, duchenne - physiopathology (5) 5
natural-history (5) 5
nutrition (5) 5
pilot projects (5) 5
research article (5) 5
trial (5) 5
united states (5) 5
animals (4) 4
diagnosis (4) 4
fatty acids (4) 4
fish (4) 4
fisheries (4) 4
genetics (4) 4
history (4) 4
international cooperation (4) 4
marine & freshwater biology (4) 4
medical research (4) 4
medicine (4) 4
muscular atrophy, spinal - physiopathology (4) 4
muscular dystrophy, duchenne - diagnosis (4) 4
neuromuscular disease (4) 4
neuromuscular diseases (4) 4
neuromuscular disorders (4) 4
noninvasive ventilation (4) 4
outcome assessment (4) 4
patients (4) 4
phenylbutyrate (4) 4
physiological aspects (4) 4
psychometrics (4) 4
quality of life (4) 4
reproducibility of results (4) 4
retrospective studies (4) 4
spinal muscular-atrophy (4) 4
standard of care (4) 4
therapy (4) 4
time factors (4) 4
type-2 (4) 4
workshops (4) 4
abstracts (3) 3
age (3) 3
arachidonic acid (3) 3
children & youth (3) 3
childrens health (3) 3
clinical trials as topic (3) 3
clinical-trials (3) 3
cohort studies (3) 3
conferences, meetings and seminars (3) 3
consensus statement (3) 3
disability evaluation (3) 3
disease (3) 3
disease progression (3) 3
double-blind (3) 3
epidemiology (3) 3
evaluation (3) 3
genetic disorders (3) 3
genotype (3) 3
gilthead seabream (3) 3
global health (3) 3
health aspects (3) 3
hospitals (3) 3
infant (3) 3
muscle (3) 3
muscular atrophy, spinal - therapy (3) 3
muscular dystrophies - congenital (3) 3
muscular dystrophies - therapy (3) 3
muscular dystrophy, duchenne - drug therapy (3) 3
muscular dystrophy, duchenne - genetics (3) 3
mutation (3) 3
north star ambulatory assessment (3) 3
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Robarts - Stacks (10) 10
UTL at Downsview - May be requested (4) 4
Trinity College (John W Graham) - Storage (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (1) 1
Gerstein Science - Stacks (1) 1
Institute for Christian Studies - Stacks (1) 1
Law (Bora Laskin) - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
Stacks (1) 1
Thomas Fisher Rare Book - May be requested at Fisher (1) 1
Trinity College (John W Graham) - Stacks (1) 1
UofT at Mississauga - Stacks (1) 1
Victoria University E.J. Pratt - Reference (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 08/2019, Volume 61, Issue 8, pp. 964 - 971
Aim To explore the clinical course of patients presenting with facioscapulohumeral dystrophy type 1 (FSHD1) in childhood, with a view to identifying areas... 
HEARING-LOSS | SMCHD1 | PAIN | MENTAL-RETARDATION | DISEASE | FSHD | PHENOTYPE | PEDIATRICS | EPILEPSY | INHERITANCE | CLINICAL NEUROLOGY | INSIGHTS
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2017, Volume 12, Issue 2, p. e0172346
Journal Article
Aquaculture Research, ISSN 1355-557X, 05/2016, Volume 47, Issue 5, pp. 1443 - 1458
Journal Article
Muscle & Nerve, ISSN 0148-639X, 04/2019, Volume 59, Issue 4, pp. 426 - 430
Introduction: The aim of the study was to assess 12 month changes in upper limb function in patients affected by spinal muscular atrophy type 2 and 3. Methods:... 
Spinal muscular atrophy | Atrophy | Muscles | Patients | Modules
Journal Article
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 08/2007, Volume 22, Issue 8, pp. 1027 - 1049
Spinal muscular atrophy is a neurodegenerative disease that requires multidisciplinary medical care. Recent progress in the understanding of molecular... 
Standard of care | Consensus statement | Spinal muscular atrophy | COMMUNITY-ACQUIRED PNEUMONIA | LEAN BODY-MASS | HIP DISLOCATION | NEUROMUSCULAR DISORDERS | standard of care | RESPIRATORY-DISTRESS | FUNCTIONAL MOTOR SCALE | WERDNIG-HOFFMANN DISEASE | NATURAL-HISTORY | CLINICAL NEUROLOGY | consensus statement | OUTCOME MEASURES | PEDIATRICS | spinal muscular atrophy | NONINVASIVE VENTILATION | Muscular Atrophy, Spinal - diagnosis | Postoperative Complications - etiology | Gastrointestinal Diseases - physiopathology | Humans | Gastrointestinal Diseases - etiology | Postoperative Complications - prevention & control | Respiratory Insufficiency - etiology | Respiratory Paralysis - therapy | Respiratory Paralysis - physiopathology | Deglutition Disorders - therapy | Child Nutrition Disorders - etiology | Respiratory Paralysis - etiology | Child Nutrition Disorders - physiopathology | Gait Disorders, Neurologic - physiopathology | Child Nutrition Disorders - prevention & control | Deglutition Disorders - etiology | Child | Deglutition Disorders - physiopathology | Respiratory Insufficiency - physiopathology | Diagnosis, Differential | Gastrointestinal Diseases - therapy | Respiratory Insufficiency - therapy | Consensus | Gait Disorders, Neurologic - therapy | Muscular Atrophy, Spinal - therapy | Muscular Atrophy, Spinal - complications | Gait Disorders, Neurologic - etiology
Journal Article