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life sciences & biomedicine (47) 47
science & technology (47) 47
clinical neurology (46) 46
neurosciences & neurology (46) 46
humans (38) 38
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muscular dystrophy (15) 15
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quality of life (13) 13
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abridged index medicus (10) 10
dystrophy (9) 9
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adolescent (8) 8
analysis (8) 8
myotonic dystrophy - physiopathology (8) 8
neurology (8) 8
child (7) 7
muscles (7) 7
muscular dystrophy, facioscapulohumeral - diagnosis (7) 7
myotonic dystrophy - diagnosis (7) 7
severity of illness index (7) 7
cross-sectional studies (6) 6
facioscapulohumeral muscular dystrophy (6) 6
medicine, experimental (6) 6
neuromuscular disease (6) 6
quality of life - psychology (6) 6
muscle, skeletal - physiopathology (5) 5
muscular dystrophy, facioscapulohumeral - physiopathology (5) 5
myotonic dystrophy - psychology (5) 5
signs and symptoms (5) 5
child, preschool (4) 4
cost of illness (4) 4
disease progression (4) 4
mobility limitation (4) 4
myasthenia gravis (4) 4
myotonic dystrophy - complications (4) 4
myotonic dystrophy type 1 (4) 4
outcome measures (4) 4
patient reported outcome measures (4) 4
patient-reported outcome measure (4) 4
patient‐reported outcome measure (4) 4
pediatrics (4) 4
prospective studies (4) 4
reproducibility of results (4) 4
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aged, 80 and over (3) 3
biomarkers (3) 3
care and treatment (3) 3
caregivers (3) 3
charcot-marie-tooth disease (3) 3
cohort studies (3) 3
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congenital myotonic dystrophy (3) 3
congenital, hereditary, and neonatal diseases and abnormalities (3) 3
disease burden (3) 3
disease control (3) 3
health surveys (3) 3
identification methods (3) 3
muscle disease (3) 3
muscle weakness - etiology (3) 3
muscle weakness - physiopathology (3) 3
myotonic disorders - genetics (3) 3
myotonic dystrophy - pathology (3) 3
myotonic dystrophy type-1 (3) 3
myotonic dystrophy type‐1 (3) 3
neurological diseases (3) 3
neuromuscular diseases (3) 3
qualitative research (3) 3
surveys and questionnaires - standards (3) 3
symptoms (3) 3
translations (3) 3
6 minute walk test (2) 2
activities of daily living (2) 2
adults (2) 2
animals (2) 2
anti-inflammatory agents - therapeutic use (2) 2
arthritis (2) 2
cellcept (2) 2
charcot marie tooth disease (2) 2
charcot-marie-tooth disease - psychology (2) 2
clinical trials as topic (2) 2
cognitive ability (2) 2
consortia (2) 2
deglutition disorders - etiology (2) 2
deglutition disorders - physiopathology (2) 2
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disease models, animal (2) 2
electrical impedance myography (2) 2
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Journal Article
The New England journal of medicine, ISSN 1533-4406, 08/2016, Volume 375, Issue 6, pp. 511 - 522
Journal Article
Neurology. Clinical practice, ISSN 2163-0402, 2018, Volume 8, Issue 6, pp. 507 - 520
Purpose of review: Myotonic dystrophy type 1 (DM1) is a severe, progressive genetic disease that affects between 1 in 3,000 and 8,000 individuals globally. No... 
Care and treatment | Adults | Research | Myotonic dystrophy | Health aspects | 199 | 185 | Review | Neurosciences | Neurovetenskaper
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 03/2015, Volume 84, Issue 10, pp. 1034 - 1042
OBJECTIVES:The objectives of this study were to develop a conceptual model of quality of life (QOL) in muscular dystrophies (MDs) and review existing QOL... 
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Quality of Life - psychology | Muscular Dystrophies - psychology | Surveys and Questionnaires - standards | Humans | Psychometrics - instrumentation | Index Medicus | Abridged Index Medicus | 176 | 112 | 113 | 185
Journal Article
Muscle & nerve, ISSN 0148-639X, 10/2014, Volume 50, Issue 4, pp. 477 - 487
Journal Article