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Scientific reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 4374 - 9
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Disease Susceptibility | Follow-Up Studies | Humans | Middle Aged | Male | Adipokines - metabolism | Amyotrophic Lateral Sclerosis - mortality | Germany - epidemiology | C-Reactive Protein - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Survival Analysis | Biomarkers | Female | Registries | Aged | Amyotrophic Lateral Sclerosis - etiology | Odds Ratio | Population Surveillance | Amyotrophic Lateral Sclerosis - epidemiology | Energy metabolism | C-reactive protein | Medical prognosis | Leptin | Amyotrophic lateral sclerosis | Population studies | Survival | Adiponectin | Smoking | Index Medicus
Journal Article
Lancet neurology, ISSN 1474-4422, 02/2020, Volume 19, Issue 2, pp. 145 - 156
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Phenotypes | Neurodegenerative diseases | Age determination | Clinical trials | Amyotrophic lateral sclerosis | Environmental factors | Studies | Literature reviews | Dementia disorders | Death | Mutation | Frontotemporal dementia | Alzheimer's disease | Age | Dementia | Index Medicus | Life Sciences | Santé publique et épidémiologie | Medicin och hälsovetenskap
Journal Article
Brain (London, England : 1878), ISSN 0006-8950, 1/2009, Volume 132, Issue 1, pp. 156 - 171
Multiple system atrophy | Progressive supranuclear palsy | Randomized controlled trial | Riluzole | Natural history | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Neuroprotective Agents - therapeutic use | Parkinson Disease, Secondary - etiology | Severity of Illness Index | Prognosis | Riluzole - adverse effects | Supranuclear Palsy, Progressive - drug therapy | Humans | Middle Aged | Male | Multiple System Atrophy - complications | Psychometrics | Treatment Outcome | Disease Progression | Supranuclear Palsy, Progressive - complications | Epidemiologic Methods | Riluzole - therapeutic use | Female | Multiple System Atrophy - drug therapy | Aged | Multiple System Atrophy - diagnosis | Neuroprotective Agents - adverse effects | Supranuclear Palsy, Progressive - diagnosis | Index Medicus | Abridged Index Medicus | Supranuclear Palsy, Progressive | Neuroprotective Agents | Parkinson Disease, Secondary | Life Sciences | Multiple System Atrophy | Santé publique et épidémiologie | multiple system atrophy | Original | natural history | riluzole | progressive supranuclear palsy | randomized controlled trial
Journal Article
Frontiers in neuroscience, ISSN 1662-4548, 08/2018, Volume 12, pp. 517 - 517
Brain-computer interface | ECAS | P300 | Amyotrophic lateral sclerosis | Cognition | Neuropsychology | Brain-machine interface | Oddball | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Usage | Research | Human-machine systems | Medical screening | Interfaces | Einstein, Albert (1879-1955) | Cognitive ability | Dementia | neuropsychology | brain–machine interface | brain–computer interface | cognition
Journal Article
Journal of neurochemistry, ISSN 0022-3042, 04/2019, Volume 149, Issue 2, pp. 168 - 169
Journal Article
Nature genetics, ISSN 1061-4036, 2009, Volume 41, Issue 10, pp. 1083 - U53
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Neurology | Cerebrospinal fluid. Meninges. Spinal cord | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Nervous system (semeiology, syndromes) | Chromosomes, Human, Pair 19 | Genome-Wide Association Study | Disease Susceptibility | Amyotrophic Lateral Sclerosis - genetics | Humans | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 9 | Genome, Human | Quantitative trait loci | Care and treatment | Amyotrophic lateral sclerosis | Genetic aspects | Disease susceptibility | Research | Single nucleotide polymorphisms | Identification and classification | Health aspects | Risk factors | Medical research | Statistical analysis | Brain research | Quality control | Genetics | Charitable foundations | Neurological disorders | Muscular dystrophy | Index Medicus | Medicin och hälsovetenskap
Journal Article
Journal of neurochemistry, ISSN 0022-3042, 04/2019, Volume 149, Issue 2, pp. 168 - 169
Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Cannabinoids | Amyotrophic Lateral Sclerosis | Animals | Humans | Male | Mice, Transgenic | Mice | Disease Models, Animal | Superoxide Dismutase | Phenols | Amyotrophic lateral sclerosis | Index Medicus
Journal Article
5/2018, Volume 11, 19
myotonic dystrophy | Alzheimer’s disease | Duchenne muscular dystrophy | antisense oligonucleotides | Huntington’s disease | nusinersen | spinal muscular atrophy | amyotrophic lateral sclerosis | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Gene expression | Neuromuscular diseases
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