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2006, 2nd ed., ISBN 0199212937, x, 352
Book
Muscle & nerve, ISSN 0148-639X, 1978
Journal
2008, 1st ed., ISBN 9780979212581, x, 271
Book
Journal of clinical neuromuscular disease, ISSN 1522-0443, 1999
Journal
Annals of the rheumatic diseases, ISSN 0003-4967, 04/2016, Volume 75, Issue 4, pp. 696 - 701
Life Sciences & Biomedicine | Rheumatology | Science & Technology | Humans | Middle Aged | Myositis, Inclusion Body - immunology | Sjogren's Syndrome - immunology | Male | Case-Control Studies | Myositis, Inclusion Body - diagnosis | Dermatomyositis - immunology | Sensitivity and Specificity | 5'-Nucleotidase - immunology | Lupus Erythematosus, Systemic - immunology | Polymyositis - diagnosis | Adult | Female | Diabetes Mellitus, Type 1 - immunology | Neuromuscular Diseases - immunology | Polymyositis - immunology | Autoimmune Diseases - immunology | Dermatomyositis - diagnosis | Scleroderma, Systemic - immunology | Autoantibodies - immunology | Multiple Sclerosis - immunology | ROC Curve | Aged | Arthritis, Rheumatoid - immunology | Inclusion body myositis | Care and treatment | Dosage and administration | Autoantibodies | Antigenic determinants | Studies | Antigens | Musculoskeletal system | Immunoglobulins | Neuromuscular diseases | Disease | Peptides | Autoimmune diseases | Scleroderma | Patients | Dementia | Index Medicus | Idiopathic inflammatory myopathy | Disease-specificity | Cytosolic 5’-nucleotidase 1A (cN-1A) | ELISA | Medicin och hälsovetenskap
Journal Article
2005, Supportive care series, ISBN 9780192631411, xvii, 540
Respiratory organs | Palliative treatment | Diseases | Patient Care and End-of-Life Decision Making | Pain Management and Palliative Pharmacology | Pulmonary disease | Breathlessness | Cardiac disease | Respiratory symptoms | Advancing disease | Incurable disease | Neuromuscular disorders | Patients | Cough | Cancer
Book
Amyotrophic lateral sclerosis, ISSN 1748-2968, 2006
Journal
2005, 4th ed., ISBN 9780721694917, Volume 1-2, 2 v. (xxiv, 2753, xcii p.)
Book
Clinical infectious diseases, ISSN 1058-4838, 3/2012, Volume 54, Issue 6, pp. 810 - 817
Human respiratory syncytial virus | Neuromuscular diseases | Predisposing factors | Respiratory syncytial viruses | Chronic diseases | Disease risk | Hospitalization | Children | Down syndrome | ARTICLES AND COMMENTARIES | Heart diseases | Infectious Diseases | Immunology | Life Sciences & Biomedicine | Microbiology | Science & Technology | Biological and medical sciences | Viral diseases of the respiratory system and ent viral diseases | Infectious diseases | Medical sciences | Human viral diseases | Viral diseases | Length of Stay | Severity of Illness Index | Humans | Risk Factors | Proportional Hazards Models | Hospitalization - statistics & numerical data | Infant | Immune System Diseases - complications | Lung Diseases, Interstitial - complications | Incidence | Immune System Diseases - congenital | Respiratory Syncytial Viruses | Neuromuscular Diseases - complications | Chromosome Aberrations | Denmark | Liver Diseases - complications | Registries | Respiratory Syncytial Virus Infections - virology | Chronic Disease | Infant, Newborn | Metabolism, Inborn Errors - complications | Respiratory Syncytial Virus Infections - complications | Cohort Studies | Respiratory syncytial virus infection | Research | Demographic aspects | Risk factors | Pediatrics | Respiratory syncytial virus | Congenital diseases | Chronic illnesses | Congenital defects | Respiratory diseases | Surgery | Metabolism | Chromosome aberrations | Siblings | Index Medicus
Journal Article
2013, ISBN 0521171857, 184
Book
2000, Experience of illness series, ISBN 0415202396, 160
eBook
2011, Clinical dysphagia series, ISBN 9781597563697, xi, 196
Book
Brain (London, England : 1878), ISSN 0006-8950, 12/2014, Volume 137, Issue 12, pp. 3235 - 3247
Lysosomal protein degradation | Mouse model | Gaucher disease | Parkinson's disease | Alpha-synuclein | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Errors of metabolism | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | Metabolic diseases | Nervous system as a whole | Medical sciences | Diseases of striated muscles. Neuromuscular diseases | Nervous system (semeiology, syndromes) | Lipids (lysosomal enzyme disorders, storage diseases) | Parkinson Disease - complications | Gene Expression | Glucosylceramidase - genetics | Genotype | Mice, Transgenic | Gaucher Disease - complications | Mice, 129 Strain | Parkinson Disease - genetics | Mutation - genetics | Phenotype | Animals | Gaucher Disease - genetics | Heterozygote | alpha-Synuclein - genetics | alpha-Synuclein - metabolism | Disease Models, Animal | Index Medicus | Abridged Index Medicus | mouse model | alpha-synuclein | Original | lysosomal protein degradation | Parkinson’s disease
Journal Article
1998, 1st ed., ISBN 9781557985118, xvii, 266
Book
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2018, Volume 72, Issue 20, pp. 2485 - 2506
arrhythmias | dystrophy | skeletal muscle | myopathy | cardiomyopathies | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | 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 | Pediatrics | Conduction | Cardiac arrhythmia | Disease | Muscular diseases | Creatine kinase | Cardiomyopathy | Disorders | Kinases | Creatine | Muscular dystrophy | Genetic screening | Defects | Eutrophication | Genotype & phenotype | Mitochondria | Glycogenosis | Ataxia | Oxidation | Bioindicators | Cardiology | Heart diseases | Age | Heart failure | Phenotypes | Neuromuscular diseases | Genetic disorders | Glycogen | Muscles | Fatty acids | Patients | Coronary artery disease | Skeletal muscle | Diseases | Storage diseases | Friedreich's ataxia | Musculoskeletal system | Medical prognosis | Family studies | Biomarkers | Lactic acid | Ventricle | Mutation
Journal Article