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Studies in health technology and informatics, ISSN 0926-9630, 2018, Volume 253, pp. 70 - 74
Journal Article
Movement disorders, ISSN 0885-3185, 07/2020, Volume 35, Issue 7, pp. 1245 - 1248
Parkinson's disease | LAMP1 | VPS13C | GBA | ATP13A2 | α‐synuclein | Lysosme | TMEM175 | chaperone‐mediated‐autophagy | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic variance | Neurodegenerative diseases | Parkinsons disease | Lysosomes | Glucosylceramidase | Genomes | Synuclein | Movement disorders | DNA sequencing | Index Medicus
Journal Article
PloS one, ISSN 1932-6203, 07/2018, Volume 13, Issue 7, pp. e0200728 - e0200728
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Neisseria - isolation & purification | Attention Deficit Disorder with Hyperactivity - microbiology | Humans | Gastrointestinal Microbiome | Male | Biodiversity | Neisseria - classification | DNA, Bacterial - genetics | Attention Deficit Disorder with Hyperactivity - genetics | Adolescent | RNA, Bacterial - genetics | RNA, Ribosomal, 16S - genetics | Child | Neisseria - genetics | DNA, Ribosomal - genetics | Care and treatment | Research | Microbiota (Symbiotic organisms) | Analysis | Attention-deficit hyperactivity disorder | Biological diversity | rRNA 16S | Mental disorders | Hyperactivity | Pathogenesis | Microbiomes | Families & family life | Psychotherapy | Alcohol | Systematic review | Mental depression | Microbiota | Microorganisms | Teenagers | Intestinal microflora | Immune system | Dopamine | Attention deficit hyperactivity disorder | Behavior disorders | Patients | Children & youth | Studies | Autism | Hospitals | Biomarkers | Cocaine | Impulsive behavior | Molecular biology | Child & adolescent psychiatry | Index Medicus
Journal Article
Movement disorders, ISSN 0885-3185, 04/2015, Volume 30, Issue 5, pp. 721 - 724
tremor | essential tremor | genetics | meta‐analysis | FUS | Genetics | Tremor | Essential tremor | Meta-analysis | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Essential Tremor - genetics | Humans | Middle Aged | RNA-Binding Protein FUS - genetics | Male | Mutation - genetics | Databases, Bibliographic - statistics & numerical data | DNA Mutational Analysis | Aged, 80 and over | Adult | Female | Aged | France | Germany | Index Medicus
Journal Article
The European respiratory journal, ISSN 0903-1936, 01/2018, Volume 51, Issue 1, pp. 1700991 - 1700991
Life Sciences & Biomedicine | Respiratory System | Science & Technology | Sarcoidosis - diagnosis | Acute Disease | Europe | Humans | Middle Aged | European Continental Ancestry Group | Genotype | Male | Lung - physiopathology | Tertiary Healthcare | Lymph Nodes - physiopathology | Abdomen | Forced Expiratory Volume | Phenotype | Sarcoidosis - physiopathology | Skin Diseases - physiopathology | Adult | Female | Aged | Lung Diseases - physiopathology | Skin - physiopathology | Eye Diseases - physiopathology | Eye - physiopathology | Joint Diseases - physiopathology | Phenotypes | Sarcoidosis | Central nervous system | Fatigue | Skin | Heart diseases | Genotypes | Lymph nodes
Journal Article
Brain (London, England : 1878), ISSN 0006-8950, 2016, Volume 139, Issue 12, pp. 3163 - 3169
Genetics | Genome-wide association study | Tremor | Essential tremor | Movement disorders | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics | Genome-Wide Association Study | Essential Tremor - genetics | Humans | Protein-Serine-Threonine Kinases - genetics | Polymorphism, Single Nucleotide | alpha Catenin - genetics | Index Medicus | Abridged Index Medicus | tremor | genetics | genome-wide association study | essential tremor | 1030 | movement disorders | Original
Journal Article
Translational neurodegeneration, ISSN 2047-9158, 04/2019, Volume 8, Issue 1, pp. 11 - 11
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Studies | Encephalitis | Medical research | Neurology | Emotional disorders | Memory | Parkinsons disease | Cognitive ability | Standard deviation | Patients | Age | Dementia | Parkinson disease | NMDA IgA/IgM antibodies | NMDA antibody | Cognitive impairment
Journal Article
Parkinsonism & related disorders, ISSN 1353-8020, 06/2020, Volume 75, pp. 24 - 26
Journal Article
Parkinsonism & related disorders, ISSN 1353-8020, 2013, Volume 20, Issue 1, pp. 134 - 135
Neurology | Genetics | Dystonia | Tremor | Essential tremor | ANO3 | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease - genetics | Essential Tremor - genetics | Humans | Middle Aged | Female | Male | Aged | Polymorphism, Single Nucleotide | Anoctamins | Chloride Channels - genetics | Reverse Transcriptase Polymerase Chain Reaction | Index Medicus
Journal Article
Movement disorders, ISSN 0885-3185, 04/2015, Volume 30, Issue 5, pp. 721 - 724
Journal Article
BMC cardiovascular disorders, ISSN 1471-2261, 01/2019, Volume 19, Issue 1, pp. 26 - 26
Delirium | Myocardial infarction | Stroke | Genome-wide association study | Acute kidney injury | Atrial fibrillation | Cardiac surgery | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Myocardial Infarction - genetics | Cytoskeletal Proteins - genetics | Humans | Middle Aged | Stroke - diagnosis | Male | Acute Kidney Injury - genetics | Cardiac Surgical Procedures - adverse effects | Stroke - genetics | Multicenter Studies as Topic | Delirium - genetics | Dual-Specificity Phosphatases - genetics | Female | Atrial Fibrillation - diagnosis | Myocardial Infarction - diagnosis | HSC70 Heat-Shock Proteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Risk Factors | Treatment Outcome | Atrial Fibrillation - genetics | Mitogen-Activated Protein Kinase Phosphatases - genetics | Randomized Controlled Trials as Topic | Phosphoprotein Phosphatases - genetics | Ryanodine Receptor Calcium Release Channel - genetics | Acute Kidney Injury - diagnosis | Aged | Polymorphism, Single Nucleotide | Delirium - diagnosis | Heart | Medical research | Genome-wide association studies | Usage | Complications | Surgery | Medicine, Experimental | Genetic aspects | Research | Heart attack | Risk factors | Oxidative stress | Cardiac arrhythmia | Heart attacks | Heart surgery | Clinical trials | Ryanodine receptors | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Fibrillation | Ischemia | Rodents | Chromosomes | Cerebral infarction | Kidneys | Mortality | Studies | Genetic variance | Coronary vessels | Quality control | Renal failure | Index Medicus
Journal Article
2016, Volume 48, Issue 9
Publication
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