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
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (196) 196
life sciences & biomedicine (184) 184
humans (175) 175
neurosciences & neurology (126) 126
neurosciences (97) 97
amyotrophic lateral sclerosis (92) 92
clinical neurology (87) 87
male (81) 81
neurology (80) 80
female (78) 78
middle aged (64) 64
aged (50) 50
adult (48) 48
animals (43) 43
biological and medical sciences (42) 42
amyotrophic lateral sclerosis - genetics (40) 40
medical sciences (35) 35
settore med/26 - neurologia (33) 33
als (30) 30
cells, cultured (24) 24
mice (24) 24
mutation (24) 24
analysis (22) 22
medicin och hälsovetenskap (22) 22
medical and health sciences (21) 21
degenerative and inherited degenerative diseases of the nervous system. leukodystrophies. prion diseases (20) 20
research (20) 20
genetic aspects (19) 19
amyotrophic lateral sclerosis - pathology (18) 18
nervous system diseases (18) 18
risk factors (17) 17
amyotrophic lateral sclerosis - diagnosis (15) 15
cohort studies (15) 15
stem cells (15) 15
biochemistry & molecular biology (14) 14
care and treatment (14) 14
disease models, animal (14) 14
genetics & heredity (14) 14
geriatrics & gerontology (14) 14
internal medicine (14) 14
abridged index medicus (13) 13
clinical medicine (13) 13
development and progression (13) 13
italy (13) 13
klinisk medicin (13) 13
patients (13) 13
psychiatry (13) 13
treatment outcome (13) 13
amyotrophic lateral sclerosis - therapy (12) 12
c9orf72 (12) 12
case-control studies (12) 12
cell biology (12) 12
cognition (12) 12
frontotemporal dementia (12) 12
fundamental and applied biological sciences. psychology (12) 12
medicine (12) 12
nervous system (12) 12
neurons - metabolism (12) 12
neuropsychological tests (12) 12
transplantation (12) 12
aged, 80 and over (11) 11
amyotrophic lateral sclerosis - complications (11) 11
cardiovascular system & cardiology (11) 11
dementia (11) 11
medical research (11) 11
medicine & public health (11) 11
medicine, experimental (11) 11
rats (11) 11
science & technology - other topics (11) 11
settore bio/12 - biochimica clinica e biologia molecolare clinica (11) 11
amyotrophic lateral sclerosis - drug therapy (10) 10
amyotrophic lateral sclerosis - physiopathology (10) 10
dna-binding proteins - genetics (10) 10
health aspects (10) 10
italy - epidemiology (10) 10
medicine, research & experimental (10) 10
motor neuron disease (10) 10
multidisciplinary sciences (10) 10
neurodegenerative diseases (10) 10
peripheral vascular disease (10) 10
phenotype (10) 10
proteins - genetics (10) 10
research & experimental medicine (10) 10
research article (10) 10
settore m-psi/08 - psicologia clinica (10) 10
surgery (10) 10
usage (10) 10
young adult (10) 10
age of onset (9) 9
cognitive ability (9) 9
genes (9) 9
genetics (9) 9
medical genetics (9) 9
mice, transgenic (9) 9
neurologi (9) 9
neuroradiology (9) 9
protein binding (9) 9
quality of life (9) 9
stroke (9) 9
superoxide dismutase - genetics (9) 9
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Clinical trials in amyotrophic lateral sclerosis: why so many negative trials and how can trials be improved?
by Mitsumoto, Hiroshi, Dr and Brooks, Benjamin R, MD and Silani, Vincenzo, MD
Lancet neurology, ISSN 1474-4422, 2014, Volume 13, Issue 11, pp. 1127 - 1138
Neurology | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neuroprotective Agents - therapeutic use | Amyotrophic Lateral Sclerosis - therapy | Stem Cell Transplantation - standards | Humans | Amyotrophic Lateral Sclerosis - diagnosis | Riluzole - therapeutic use | Stem Cell Transplantation - trends | Randomized Controlled Trials as Topic - trends | Randomized Controlled Trials as Topic - standards | Clinical trials | Amyotrophic lateral sclerosis | Neurosciences | Riluzole | Stem cells | FDA approval | Pharmaceutical industry | Drug therapy | Rodents | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text New technologies and Amyotrophic Lateral Sclerosis – Which step forward rushed by the COVID-19 pandemic?
by Pinto, Susana and Quintarelli, Stefano and Silani, Vincenzo
Journal of the neurological sciences, ISSN 0022-510X, 11/2020, Volume 418, pp. 117081 - 117081
COVID-19 | Telemedicine | Eye-tracking | Virtual reality | Amyotrophic lateral sclerosis | Brain-computer interfaces | Artificial intelligence | Robotics | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Pandemics | Amyotrophic Lateral Sclerosis - therapy | Health Services Accessibility | Humans | Telemedicine - methods | Inventions - legislation & jurisprudence | COVID-19 - epidemiology | Epidemics | Nervous system diseases | Analysis | World health | Machine learning | Development and progression | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text TDP‐43 is recruited to stress granules in conditions of oxidative insult
by Colombrita, Claudia and Zennaro, Eleonora and Fallini, Claudia and Weber, Markus and Sommacal, Andreas and Buratti, Emanuele and Silani, Vincenzo and Ratti, Antonia
Journal of neurochemistry, ISSN 0022-3042, 11/2009, Volume 111, Issue 4, pp. 1051 - 1061
stress granules | Transactive response DNA‐binding protein 43 | RNA‐binding protein | amyotrophic lateral sclerosis | Amyotrophic lateral sclerosis | RNA-binding protein | Transactive response DNA-binding protein 43 | Stress granules | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Neurology | Biological and medical sciences | Medical sciences | Cerebrospinal fluid. Meninges. Spinal cord | Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases | Nervous system (semeiology, syndromes) | Arsenites - pharmacology | ELAV-Like Protein 1 | RNA, Small Interfering - genetics | Spinal Cord - metabolism | Emetine - pharmacology | Hybrid Cells | Oxidative Stress - physiology | Protein Transport - drug effects | ELAV Proteins | DNA-Binding Proteins - metabolism | Transfection - methods | Teratogens - pharmacology | Spinal Cord - pathology | Antigens, Surface - metabolism | Protein Synthesis Inhibitors - pharmacology | Motor Neurons - drug effects | Hot Temperature - adverse effects | Oxidative Stress - genetics | Ribonucleoproteins - metabolism | DNA-Binding Proteins - genetics | Motor Neurons - metabolism | Amyotrophic Lateral Sclerosis - pathology | Animals | Mice | Oxidative Stress - drug effects | RNA-Binding Proteins - metabolism | Protein Structure, Tertiary - drug effects | RNA, Small Interfering - metabolism | Messenger RNA | Snow | Neurons | Analysis | Genetically modified organisms | Protein biosynthesis | Binding proteins | Proteins | Brain | Biochemistry | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) – revised report of an EFNS task force
by Andersen, Peter M and Abrahams, Sharon and Borasio, Gian D and de Carvalho, Mamede and Chio, Adriano and Van Damme, Philip and Hardiman, Orla and Kollewe, Katja and Morrison, Karen E and Petri, Susanne and Pradat, Pierre‐Francois and Silani, Vincenzo and Tomik, Barbara and Wasner, Maria and Weber, Markus and EFNS Task Force Diag Management and EFNS Task Force on Diagnosis and Management of Amyotrophic Lateral Sclerosis
European journal of neurology, ISSN 1351-5101, 03/2012, Volume 19, Issue 3, pp. 360 - 375
drooling | genetic counselling | bronchial secretions | nutrition | breaking the diagnosis | caregiver | ventilation | ALS | terminal care | cognitive dysfunction | Evidence‐based medicine | palliative care | Nutrition | Bronchial secretions | Caregiver | Palliative care | Terminal care | Ventilation | Breaking the diagnosis | Drooling | Evidence-based medicine | Genetic counselling | Cognitive dysfunction | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Amyotrophic Lateral Sclerosis - diagnosis | Evidence-Based Medicine | Amyotrophic Lateral Sclerosis - therapy | Humans | Advisory Committees | Caregivers | Practice guidelines (Medicine) | Amyotrophic lateral sclerosis | Task forces | Medical genetics | Ostomy | Mucus | Survival | Emotions | Feeding | Neurophysiology | Quality of life | Pain | Reviews | Lability | spasticity | Autonomy | Books | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Therapy in Amyotrophic lateral sclerosis (ALS): An unexpected evolving scenario
by Silani, Vincenzo
Archives italiennes de biologie, ISSN 0003-9829, 2017, Volume 155, Issue 4, pp. 228 - 241
Therapy | Randomised controlled trials | Amyotrophic lateral sclerosis | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology
Journal Article
Details down arrow
6. Full Text A susceptibility-weighted imaging qualitative score of the motor cortex may be a useful tool for distinguishing clinical phenotypes in amyotrophic lateral sclerosis
by Giorgio, Conte and Sara, Sbaraini and Claudia, Morelli and Silvia, Casale and Luca, Caschera and Elisa, Contarino Valeria and Elisa, Scola and Claudia, Cinnante and Francesca, Trogu and Fabio, Triulzi and Vincenzo, Silani
European radiology, ISSN 0938-7994, 09/2020, Volume 31, Issue 3, pp. 1281 - 1289
Life Sciences & Biomedicine | Radiology, Nuclear Medicine & Medical Imaging | Science & Technology | Amyotrophic lateral sclerosis | Neurosciences | Genetic aspects | Diagnostic imaging | Neuroimaging | Phenotypes | Medical imaging | Susceptibility | Cortex | Impairment | Cortex (motor) | Subgroups | Mimicry | Magnetic resonance imaging | Magnetic permeability | Diagnostic systems | Diagnosis | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Neurochemical biomarkers in amyotrophic lateral sclerosis
by Verde, Federico and Silani, Vincenzo and Otto, Markus
Current opinion in neurology, ISSN 1350-7540, 10/2019, Volume 32, Issue 5, pp. 747 - 757
Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Biomarkers - metabolism | Diagnosis, Differential | Phosphorylation | Prognosis | Humans | Amyotrophic Lateral Sclerosis - metabolism | Amyotrophic Lateral Sclerosis - diagnosis | Neurofilament Proteins - metabolism | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights