X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (327) 327
Publication (65) 65
Book Review (31) 31
Book Chapter (8) 8
Conference Proceeding (6) 6
Book / eBook (2) 2
Magazine Article (1) 1
Report (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (204) 204
humans (199) 199
amyotrophic lateral sclerosis (152) 152
clinical neurology (127) 127
amyotrophic lateral sclerosis - genetics (99) 99
male (98) 98
female (94) 94
neurosciences (87) 87
als (78) 78
middle aged (71) 71
aged (70) 70
neurology (63) 63
disease (52) 52
amyotrophic-lateral-sclerosis (51) 51
motor-neuron disease (51) 51
genetic aspects (47) 47
adult (46) 46
mutation (44) 44
risk factors (42) 42
amyotrophic lateral sclerosis - epidemiology (40) 40
genetics (39) 39
genetic predisposition to disease (38) 38
genes (37) 37
mutations (37) 37
case-control studies (35) 35
genome-wide association (35) 35
analysis (33) 33
genetics & heredity (33) 33
polymorphism, single nucleotide (33) 33
aged, 80 and over (32) 32
genome-wide association study (32) 32
amyotrophic lateral sclerosis - diagnosis (31) 31
dementia (30) 30
epidemiology (30) 30
research (30) 30
medicin och hälsovetenskap (29) 29
survival (29) 29
frontotemporal dementia (28) 28
gene (28) 28
medical and health sciences (28) 28
population (28) 28
risk (28) 28
diagnosis (27) 27
article (26) 26
genotype (26) 26
medical research (26) 26
psychiatry (26) 26
motor neuron disease (25) 25
animals (24) 24
genomes (24) 24
hexanucleotide repeat (24) 24
biochemistry & molecular biology (22) 22
genomics (22) 22
proteins (22) 22
c9orf72 (21) 21
geriatrics & gerontology (21) 21
internal medicine (21) 21
neurodegeneration (21) 21
susceptibility (21) 21
cohort studies (20) 20
nervous system diseases (19) 19
studies (19) 19
abridged index medicus (18) 18
amyotrophic lateral sclerosis - pathology (18) 18
amyotrophic lateral sclerosis - therapy (18) 18
association (18) 18
frontotemporal lobar degeneration (18) 18
neurodegenerative diseases (18) 18
amyotrophic lateral sclerosis - mortality (17) 17
amyotrophic lateral sclerosis - physiopathology (17) 17
neurons (17) 17
superoxide dismutase - genetics (17) 17
surgery (17) 17
health aspects (16) 16
phenotype (16) 16
survival analysis (16) 16
variants (16) 16
age of onset (15) 15
disease progression (15) 15
genetic predisposition to disease - genetics (15) 15
klinisk medicin (15) 15
multidisciplinary sciences (15) 15
neurologi (15) 15
patients (15) 15
sclerosis (15) 15
superoxide dismutase-1 (15) 15
alzheimers disease (14) 14
amyotrophic lateral sclerosis - complications (14) 14
care and treatment (14) 14
clinical medicine (14) 14
genetic variation (14) 14
alleles (13) 13
genetic association studies (13) 13
linkage disequilibrium (13) 13
medicine, experimental (13) 13
motor neurons (13) 13
research article (13) 13
clinical trials (12) 12
genetic research (12) 12
haplotypes (12) 12
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2010, ISBN 9780879698836, ix, 220
Book
Nature, ISSN 0028-0836, 10/2017, Volume 550, Issue 7676, pp. S112 - S112
The terms familial ALS and sporadic ALS are outdated and illogical. They impede research, confuse patients and cloud our thinking. It's time to ditch them. 
Amyotrophic lateral sclerosis | Family medical history | Mutation
Journal Article
Journal Article
New England Journal of Medicine, ISSN 0028-4793, 10/2017, Volume 377, Issue 16, p. 1602
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2014, Volume 13, Issue 11, pp. 1108 - 1113
Journal Article
Nature, ISSN 0028-0836, 10/2017, Volume 550, Issue 7676, pp. S112 - S112
Journal Article
Lancet, The, ISSN 0140-6736, 2014, Volume 383, Issue 9934, pp. 2028 - 2030
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/S0140-6736(14)60270-1 Byline: Ammar Al-Chalabi (a) 
Internal Medicine | TRIAL | DOUBLE-BLIND | MEDICINE, GENERAL & INTERNAL | PLACEBO | LITHIUM | DEXPRAMIPEXOLE | Enteral Nutrition - methods | Female | Male | Amyotrophic Lateral Sclerosis - therapy | Humans | Amyotrophic lateral sclerosis | Diet | Metabolism | Patients | Medical prognosis | Index Medicus | Abridged Index Medicus
Journal Article
Epidemiology, ISSN 1044-3983, 11/2015, Volume 26, Issue 6, pp. 821 - 823
Journal Article
The Lancet Neurology, ISSN 1474-4422, 01/2019, Volume 18, Issue 1, pp. 12 - 13
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 12/2011, Volume 122, Issue 6, pp. 691 - 702
Neuronal cytoplasmic inclusions (NCIs) containing phosphorylated TDP-43 (p-TDP-43) are the pathological hallmarks of motor neuron disease/amyotrophic lateral... 
C9 orf 72 | TDP43 | Pathology | Neurosciences | MND/ALS | Medicine & Public Health | FTLD | p62 | C9orf72 | PROGRANULIN GENE | DEMENTIA | UBIQUITIN | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY | DISEASE | FTD | MUTATIONS | HEXANUCLEOTIDE REPEAT | Frontotemporal Lobar Degeneration - pathology | Neurons - pathology | Pyramidal Cells - metabolism | DNA Repeat Expansion - genetics | Sequestosome-1 Protein | Humans | Middle Aged | Male | Case-Control Studies | DNA-Binding Proteins - metabolism | Aged, 80 and over | Adult | Female | C9orf72 Protein | Neurons - metabolism | Inclusion Bodies - metabolism | Purkinje Cells - metabolism | Amyotrophic Lateral Sclerosis - genetics | Cerebellum - metabolism | Hippocampus - pathology | DNA-Binding Proteins - genetics | Mutation - genetics | Cerebellum - pathology | Intranuclear Inclusion Bodies - pathology | DNA - genetics | Proteins - genetics | Hippocampus - metabolism | Amyotrophic Lateral Sclerosis - pathology | Adaptor Proteins, Signal Transducing - genetics | Inclusion Bodies - pathology | Pyramidal Cells - pathology | Aged | Frontotemporal Lobar Degeneration - genetics | Adaptor Proteins, Signal Transducing - metabolism | Purkinje Cells - pathology | Intranuclear Inclusion Bodies - metabolism | Ubiquitin | Brain | School facilities | Neurons | Amyotrophic lateral sclerosis | Universities and colleges | Education parks | Protein binding | Index Medicus
Journal Article
Nature Reviews Neurology, ISSN 1759-4758, 01/2014, Volume 10, Issue 10, pp. 549 - 550
Amyotrophic lateral sclerosis (ALS) shows complex inheritance. A new meta-analysis of three data sets has replicated previous estimates of the heritability... 
Amyotrophic lateral sclerosis | Development and progression | Genetic aspects | Genetic variation | Identification and classification
Journal Article
Science, ISSN 0036-8075, 2/2009, Volume 323, Issue 5918, pp. 1208 - 1211
Journal Article
Science, ISSN 0036-8075, 3/2008, Volume 319, Issue 5870, pp. 1668 - 1672
Journal Article