Articles

UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (5450) 5450
Magazine Article (10) 10
Book / eBook (8) 8
Newsletter (5) 5
Book Chapter (4) 4
Dissertation (4) 4
Newspaper Article (4) 4
Conference Proceeding (3) 3
Publication (3) 3
Streaming Video (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (4741) 4741
science & technology (3806) 3806
life sciences & biomedicine (3680) 3680
male (3267) 3267
female (2978) 2978
neurosciences & neurology (2555) 2555
adult (2143) 2143
middle aged (1901) 1901
neurosciences (1675) 1675
neurology (1673) 1673
clinical neurology (1668) 1668
biological and medical sciences (1605) 1605
medical sciences (1503) 1503
ataxia (1472) 1472
ataxia - physiopathology (1233) 1233
animals (1171) 1171
aged (1137) 1137
adolescent (905) 905
cerebellar ataxia - physiopathology (870) 870
child (793) 793
magnetic resonance imaging (667) 667
abridged index medicus (574) 574
mice (553) 553
nervous system (550) 550
cerebellum (543) 543
spinocerebellar ataxias - physiopathology (535) 535
degenerative and inherited degenerative diseases of the nervous system. leukodystrophies. prion diseases (513) 513
mutation (502) 502
friedreich ataxia - physiopathology (489) 489
ataxia - etiology (478) 478
cerebellum - physiopathology (454) 454
child, preschool (402) 402
phenotype (391) 391
spinocerebellar ataxias - genetics (371) 371
cerebellar ataxia (368) 368
young adult (363) 363
ataxia - genetics (357) 357
cerebellum - pathology (343) 343
disease models, animal (325) 325
pedigree (321) 321
analysis (320) 320
diagnosis, differential (306) 306
syndrome (300) 300
brain - pathology (299) 299
spinocerebellar ataxia (298) 298
electromyography (290) 290
research (289) 289
disease progression (288) 288
genetic aspects (285) 285
ataxia - diagnosis (279) 279
cerebellar ataxia - genetics (275) 275
age of onset (252) 252
severity of illness index (245) 245
brain - physiopathology (243) 243
genetics & heredity (239) 239
nerve tissue proteins - genetics (233) 233
gait (231) 231
treatment outcome (229) 229
aged, 80 and over (228) 228
brain (228) 228
biomedicine (224) 224
ataxia telangiectasia - physiopathology (218) 218
psychomotor performance - physiology (216) 216
nervous system diseases (215) 215
time factors (214) 214
psychiatry (211) 211
cerebellar ataxia - diagnosis (204) 204
research article (203) 203
pediatrics (201) 201
surgery (200) 200
medical genetics (199) 199
patients (199) 199
fundamental and applied biological sciences. psychology (198) 198
electroencephalography (197) 197
friedreich ataxia - genetics (189) 189
proteins (186) 186
mutation - genetics (183) 183
biochemistry & molecular biology (182) 182
ataxia - pathology (180) 180
atrophy (180) 180
diagnosis (174) 174
neurodegeneration (173) 173
case-control studies (172) 172
neurobiology (172) 172
neuropsychological tests (172) 172
cerebellar diseases - physiopathology (171) 171
ataxia - complications (170) 170
infant (167) 167
rats (165) 165
risk factors (165) 165
care and treatment (164) 164
fragile x syndrome - physiopathology (164) 164
friedreich's ataxia (164) 164
rehabilitation (163) 163
genetics (161) 161
medicine & public health (161) 161
neurologic examination (161) 161
medicine (160) 160
physiological aspects (160) 160
medical research (158) 158
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (5106) 5106
Japanese (162) 162
French (102) 102
Spanish (83) 83
German (55) 55
Russian (42) 42
Portuguese (17) 17
Italian (15) 15
Polish (9) 9
Dutch (7) 7
Hungarian (5) 5
Chinese (4) 4
Ukrainian (2) 2
Czech (1) 1
Hebrew (1) 1
Norwegian (1) 1
Serbian (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Movement Disorders in Treatable Inborn Errors of Metabolism
by Ebrahimi‐Fakhari, Darius and Van Karnebeek, Clara and Münchau, Alexander
Movement disorders, ISSN 0885-3185, 05/2019, Volume 34, Issue 5, pp. 598 - 613
inborn errors of metabolism | treatment | movement disorders | neurotransmitter disorders | neurogenetics | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amino Acid Metabolism, Inborn Errors - complications | Niemann-Pick Disease, Type C - therapy | Hepatolenticular Degeneration - therapy | Monosaccharide Transport Proteins - deficiency | Amino Acid Metabolism, Inborn Errors - physiopathology | Humans | Folic Acid Deficiency - therapy | Hepatolenticular Degeneration - physiopathology | Vitamin E Deficiency - therapy | Dystonic Disorders - complications | Brain Diseases, Metabolic - diagnosis | Vitamin E Deficiency - diagnosis | Xanthomatosis, Cerebrotendinous - diagnosis | Basal Ganglia Diseases - diagnosis | Carbohydrate Metabolism, Inborn Errors - therapy | Dystonia - etiology | Carbohydrate Metabolism, Inborn Errors - diagnosis | Parkinsonian Disorders - physiopathology | Chorea - physiopathology | Dystonia - physiopathology | Metabolic Diseases - diagnosis | Ataxia - diagnosis | Carbohydrate Metabolism, Inborn Errors - physiopathology | Metabolism, Inborn Errors - diagnosis | Folic Acid Deficiency - complications | Movement Disorders - physiopathology | Brain Diseases, Metabolic - physiopathology | Basal Ganglia Diseases - therapy | Ataxia - complications | Muscle Spasticity - physiopathology | Xanthomatosis, Cerebrotendinous - complications | Metabolic Diseases - complications | Metabolism, Inborn Errors - complications | Metabolism, Inborn Errors - physiopathology | Brain Diseases, Metabolic - complications | Glutaryl-CoA Dehydrogenase - deficiency | Carbohydrate Metabolism, Inborn Errors - complications | Ataxia - etiology | Hepatolenticular Degeneration - diagnosis | Metabolism, Inborn Errors - therapy | Niemann-Pick Disease, Type C - physiopathology | Parkinsonian Disorders - etiology | Amino Acid Metabolism, Inborn Errors - diagnosis | Brain Diseases, Metabolic - therapy | Xanthomatosis, Cerebrotendinous - therapy | Metabolic Diseases - therapy | Metabolic Diseases - physiopathology | Myoclonus - etiology | Vitamin E Deficiency - complications | Niemann-Pick Disease, Type C - diagnosis | Dystonic Disorders - physiopathology | Dystonic Disorders - therapy | Hepatolenticular Degeneration - complications | Vitamin E Deficiency - physiopathology | Ataxia - physiopathology | Ataxia - therapy | Chorea - etiology | Amino Acid Metabolism, Inborn Errors - therapy | Basal Ganglia Diseases - complications | Folic Acid Deficiency - physiopathology | Myoclonus - physiopathology | Muscle Spasticity - etiology | Dystonic Disorders - diagnosis | Basal Ganglia Diseases - physiopathology | Movement Disorders - etiology | Xanthomatosis, Cerebrotendinous - physiopathology | Folic Acid Deficiency - diagnosis | Niemann-Pick Disease, Type C - complications | Dystonic Disorders - etiology | Metabolism, Inborn errors of | Education | Mortality | Finance | Physiological aspects | Creatine | Movement disorders | Energy metabolism | Inborn errors of metabolism | Lysosomal storage diseases | Metabolism | Autophagy | Morbidity | Quality of life | Phenomenology | Psychiatrists | Differential diagnosis | Children | Phagocytosis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Genetic mimics of cerebral palsy
by Pearson, Toni S and Pons, Roser and Ghaoui, Roula and Sue, Carolyn M
Movement disorders, ISSN 0885-3185, 05/2019, Volume 34, Issue 5, pp. 625 - 636
cerebral palsy | inborn errors of metabolism | spasticity | ataxia | dystonia | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Brain - diagnostic imaging | Monosaccharide Transport Proteins - deficiency | Lesch-Nyhan Syndrome - therapy | Spastic Paraplegia, Hereditary - diagnosis | Humans | Movement Disorders - diagnosis | Folic Acid Deficiency - therapy | Lesch-Nyhan Syndrome - genetics | Cerebral Palsy - diagnosis | Multiple Carboxylase Deficiency - genetics | Carbohydrate Metabolism, Inborn Errors - therapy | Brain Diseases, Metabolic, Inborn - genetics | Dyskinesias - genetics | Folic Acid Deficiency - genetics | Multiple Carboxylase Deficiency - physiopathology | Carbohydrate Metabolism, Inborn Errors - diagnosis | Monosaccharide Transport Proteins - genetics | Chorea - physiopathology | Creatine - genetics | Hyperargininemia - physiopathology | Dyskinesias - physiopathology | Dystonia - physiopathology | Pelizaeus-Merzbacher Disease - diagnosis | Plasma Membrane Neurotransmitter Transport Proteins - genetics | Carbohydrate Metabolism, Inborn Errors - physiopathology | Magnetic Resonance Imaging | Hyperargininemia - diagnosis | Movement Disorders - physiopathology | Dyskinesias - diagnosis | Hyperargininemia - genetics | Ataxia Telangiectasia - genetics | Lesch-Nyhan Syndrome - diagnosis | Brain Diseases, Metabolic, Inborn - therapy | Muscle Spasticity - physiopathology | Movement Disorders - genetics | Multiple Carboxylase Deficiency - diagnosis | Multiple Carboxylase Deficiency - therapy | GTP-Binding Protein alpha Subunits, Gi-Go - genetics | Spastic Paraplegia, Hereditary - genetics | Cerebral Palsy - physiopathology | Lesch-Nyhan Syndrome - physiopathology | Mental Retardation, X-Linked - physiopathology | Carbohydrate Metabolism, Inborn Errors - genetics | Brain Diseases, Metabolic, Inborn - diagnosis | Mental Retardation, X-Linked - genetics | Mental Retardation, X-Linked - diagnosis | Hyperargininemia - therapy | Creatine - deficiency | Thyroid Nuclear Factor 1 - genetics | Pelizaeus-Merzbacher Disease - therapy | Spastic Paraplegia, Hereditary - physiopathology | Mental Retardation, X-Linked - therapy | Ataxia Telangiectasia - diagnosis | Ataxia Telangiectasia - physiopathology | Plasma Membrane Neurotransmitter Transport Proteins - deficiency | Ataxia - physiopathology | Ataxia Telangiectasia - therapy | Diagnosis, Differential | Pelizaeus-Merzbacher Disease - genetics | Spastic Paraplegia, Hereditary - therapy | Brain Diseases, Metabolic, Inborn - physiopathology | Folic Acid Deficiency - physiopathology | Dyskinesias - therapy | Movement Disorders - therapy | Pelizaeus-Merzbacher Disease - physiopathology | Folic Acid Deficiency - diagnosis | Adenylyl Cyclases - genetics | Cerebral palsy | Development and progression | Medical genetics | Neuroimaging | Genetic counseling | Etiology | Chorea | Spasticity | Ataxia | Dystonia | Children | Paralysis | Neurodevelopmental disorders | Metabolic disorders | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Neurological and Neuropsychiatric Impacts of COVID-19 Pandemic
by Roy, Devlina and Ghosh, Ritwik and Dubey, Souvik and Dubey, Mahua Jana and Benito-Leon, Julian and Kanti Ray, Biman
Canadian journal of neurological sciences, ISSN 0317-1671, 01/2021, Volume 48, Issue 1, pp. 9 - 24
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Meningoencephalitis - physiopathology | Parkinson Disease - therapy | Headache - etiology | Demyelinating Diseases - therapy | Humans | Cerebellar Ataxia - etiology | Ageusia - physiopathology | Meningoencephalitis - etiology | COVID-19 - psychology | Anosmia - etiology | Muscular Diseases - etiology | Ageusia - etiology | Cerebellar Ataxia - physiopathology | Nervous System Diseases - epidemiology | Seizures - physiopathology | SARS-CoV-2 | COVID-19 - complications | Muscular Diseases - physiopathology | Myelitis, Transverse - physiopathology | Myoclonus - etiology | Brain Diseases | Nervous System Diseases - physiopathology | Viral Tropism | COVID-19 - epidemiology | Stroke - therapy | Myelitis, Transverse - etiology | Cerebrovascular Disorders - physiopathology | Comorbidity | Alzheimer Disease - therapy | Guillain-Barre Syndrome - physiopathology | COVID-19 - physiopathology | Headache - physiopathology | Polyneuropathies - physiopathology | Cerebrovascular Disorders - etiology | Myoclonus - physiopathology | Hypoxia, Brain - physiopathology | Angiotensin-Converting Enzyme 2 | Dizziness - etiology | Dizziness - physiopathology | Polyneuropathies - etiology | Anosmia - physiopathology | Delivery of Health Care | Guillain-Barre Syndrome - etiology | Seizures - etiology | Nervous System Diseases - etiology | Disease Management | Epilepsy - therapy | Inflammation - physiopathology | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text Development of the clinical assessment scale in autoimmune encephalitis
by Lim, Jung‐Ah and Lee, Soon‐Tae and Moon, Jangsup and Jun, Jin‐Sun and Kim, Tae‐Joon and Shin, Yong‐Won and Abdullah, Suhailah and Byun, Jung‐Ick and Sunwoo, Jun‐Sang and Kim, Keun Tae and Yang, Tae‐Won and Lee, Woo‐Jin and Moon, Hye‐Jin and Kim, Dong Wook and Lim, Byung Chan and Cho, Yong Won and Yang, Tae‐Ho and Kim, Hee Jin and Kim, Young‐Soo and Koo, Yong Seo and Park, Byeongsu and Jung, Keun‐Hwa and Kim, Manho and Park, Kyung‐Il and Jung, Ki‐Young and Chu, Kon and Lee, Sang Kun
Annals of neurology, ISSN 0364-5134, 03/2019, Volume 85, Issue 3, pp. 352 - 358
Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Anti-N-Methyl-D-Aspartate Receptor Encephalitis - psychology | Autoimmune Diseases - physiopathology | Memory Disorders - physiopathology | Autoimmune Diseases of the Nervous System - psychology | Humans | Middle Aged | Ataxia - etiology | Limbic Encephalitis - complications | Male | Language Disorders - physiopathology | Aggression - psychology | Young Adult | Anti-N-Methyl-D-Aspartate Receptor Encephalitis - physiopathology | Autoimmune Diseases of the Nervous System - physiopathology | Seizures - physiopathology | Encephalitis - physiopathology | Encephalomyelitis, Acute Disseminated - complications | Gait Disorders, Neurologic - physiopathology | Adult | Female | Encephalitis - complications | Dystonia - etiology | Limbic Encephalitis - physiopathology | Encephalitis - psychology | Muscle Weakness - etiology | Severity of Illness Index | Ataxia - physiopathology | Reproducibility of Results | Autoimmune Diseases - psychology | Limbic Encephalitis - psychology | Autoimmune Diseases - complications | Delusions - psychology | Dyskinesias - physiopathology | Dystonia - physiopathology | Encephalomyelitis, Acute Disseminated - physiopathology | Anti-N-Methyl-D-Aspartate Receptor Encephalitis - complications | Dyskinesias - etiology | Autoimmune Diseases of the Nervous System - complications | Hallucinations - psychology | Language Disorders - etiology | Encephalomyelitis, Acute Disseminated - psychology | Memory Disorders - etiology | Adolescent | Seizures - etiology | Aged | Muscle Weakness - physiopathology | Gait Disorders, Neurologic - etiology | Correlation coefficient | Encephalitis | Signs and symptoms | Stability | Gait | Mental disorders | Brain stem | Correlation coefficients | Consistency | Patients | Acceptability | Validity | Reproducibility | Correlation analysis | Ataxia | Dystonia | Autoimmune diseases | Reliability | Dyskinesia | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Clinical and immunological characteristics of the spectrum of GFAP autoimmunity: a case series of 22 patients
by Iorio, Raffaele and Damato, Valentina and Evoli, Amelia and Gessi, Marco and Gaudino, Simona and Di Lazzaro, Vincenzo and Spagni, Gregorio and Sluijs, Jacqueline A and Hol, Elly M
Journal of neurology, neurosurgery and psychiatry, ISSN 0022-3050, 02/2018, Volume 89, Issue 2, pp. 138 - 146
Journal Article | autoimmune encephalitis | autoimmune neurology | meningoencephalitis | astrocytes | autoantibodies | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Surgery | Science & Technology | Meningoencephalitis - physiopathology | Glial Fibrillary Acidic Protein - genetics | Brain - diagnostic imaging | Humans | Middle Aged | Movement Disorders - immunology | Male | Plasma Exchange | Ovarian Neoplasms - complications | Cerebellar Ataxia - immunology | Meningoencephalitis - immunology | Young Adult | Autoimmune Diseases of the Nervous System - physiopathology | Carcinoma - complications | Myelitis - immunology | Immunotherapy | Encephalomyelitis - therapy | Aged, 80 and over | Child | Myoclonus - immunology | Myelitis - physiopathology | Spinal Cord - diagnostic imaging | Autoimmune Diseases of the Nervous System - complications | Mice, Knockout | Myelitis - complications | Magnetic Resonance Imaging | Meningoencephalitis - complications | Cerebellar Ataxia - complications | Cerebellar Ataxia - therapy | Movement Disorders - physiopathology | Drug Resistant Epilepsy - immunology | Immunoglobulins, Intravenous - therapeutic use | Protein Isoforms | Adolescent | Drug Resistant Epilepsy - therapy | Mice | Myoclonus - therapy | Glucocorticoids - therapeutic use | Glial Fibrillary Acidic Protein - immunology | Cerebellar Ataxia - physiopathology | Myoclonus - complications | Encephalomyelitis - complications | Encephalomyelitis - physiopathology | Adult | Female | Optic Neuritis - immunology | Optic Neuritis - complications | Optic Neuritis - therapy | Myoclonus - physiopathology | Movement Disorders - complications | Thymus Neoplasms - complications | Autoimmune Diseases of the Nervous System - immunology | Breast Neoplasms - complications | Autoantibodies - immunology | Drug Resistant Epilepsy - complications | Animals | Movement Disorders - therapy | Optic Neuritis - physiopathology | Encephalomyelitis - immunology | Meningoencephalitis - therapy | Aged | Autoimmune Diseases of the Nervous System - therapy | Myelitis - therapy | Thymoma - complications | Drug Resistant Epilepsy - physiopathology | Immunologic Factors - therapeutic use | Autoimmunity | Usage | Care and treatment | Autoantibodies | Autoimmune diseases | Analysis | Encephalitis | Brain | Antigens | Multiple sclerosis | Immunoglobulins | Spinal cord | Dendritic cells | Disease | Epilepsy | Aquaporins | Cognitive ability | Nervous system | Drug resistance | Patients | Proteins | Immunology | Microscopy | Rheumatoid arthritis | Rodents | Ataxia | Animal cognition | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Frequent neurologic manifestations and encephalopathy‐associated morbidity in Covid‐19 patients
by Liotta, Eric M and Batra, Ayush and Clark, Jeffrey R and Shlobin, Nathan A and Hoffman, Steven C and Orban, Zachary S and Koralnik, Igor J
Annals of clinical and translational neurology, ISSN 2328-9503, 11/2020, Volume 7, Issue 11, pp. 2221 - 2230
Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Pandemics | Prognosis | Humans | Middle Aged | Coronavirus Infections - physiopathology | Male | Coronavirus Infections - mortality | Stroke - physiopathology | Brain Diseases - physiopathology | COVID-19 | Seizures - physiopathology | SARS-CoV-2 | Dysgeusia - physiopathology | Aged, 80 and over | Betacoronavirus | Adult | Female | Retrospective Studies | Severity of Illness Index | Ataxia - physiopathology | Myalgia - physiopathology | Chicago | Pneumonia, Viral - therapy | Mortality | Risk Factors | Headache - physiopathology | Respiration, Artificial | Pneumonia, Viral - physiopathology | Movement Disorders - physiopathology | Dizziness - physiopathology | Coronavirus Infections - therapy | Olfaction Disorders - physiopathology | Aged | Pneumonia, Viral - mortality | Delirium | Ventilators | Laboratories | Hispanic Americans | Infections | Hospitalization | Coronaviruses | Patients | Variables | Hospitals | Respiratory diseases | Kidney diseases | Neurological disorders | Cerebrovascular disease | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Second consensus statement on the diagnosis of multiple system atrophy
by Gilman, S and Wenning, G.K and Low, P.A and Brooks, D.J and Mathias, C.J and Trojanowski, J.Q and Wood, N.W and Colosimo, C and Dürr, A and Fowler, C.J and Kaufmann, H and Klockgether, T and Lees, A and Poewe, W and Quinn, N and Revesz, T and Robertson, D and Sandroni, P and Seppi, K and Vidailhet, M
Neurology, ISSN 0028-3878, 08/2008, Volume 71, Issue 9, pp. 670 - 676
Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Parkinsonian Disorders - physiopathology | Diagnosis, Differential | Basal Ganglia - physiopathology | Brain - physiopathology | Parkinsonian Disorders - diagnosis | Basal Ganglia - pathology | Cerebellum - physiopathology | Autonomic Nervous System Diseases - diagnosis | Cerebellum - pathology | Cerebellar Ataxia - physiopathology | Autonomic Nervous System Diseases - physiopathology | Brain - pathology | Inclusion Bodies - pathology | Multiple System Atrophy - diagnosis | Multiple System Atrophy - physiopathology | Inclusion Bodies - metabolism | Cerebellar Ataxia - diagnosis | alpha-Synuclein - metabolism | Index Medicus | Abridged Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights