X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
amyotrophic lateral sclerosis (14) 14
humans (14) 14
amyotrophic lateral sclerosis - genetics (13) 13
index medicus (11) 11
genetic aspects (8) 8
neurosciences (8) 8
aged (7) 7
female (7) 7
male (7) 7
middle aged (7) 7
mutations (7) 7
polymorphism, single nucleotide (7) 7
article (6) 6
cohort studies (6) 6
genotype (6) 6
neurology (6) 6
population (6) 6
adult (5) 5
als (5) 5
amyotrophic-lateral-sclerosis (5) 5
case-control studies (5) 5
gene expression (5) 5
genetic predisposition to disease (5) 5
susceptibility (5) 5
aged, 80 and over (4) 4
alleles (4) 4
clinical neurology (4) 4
dementia (4) 4
frontotemporal lobar degeneration (4) 4
genes (4) 4
genetics & heredity (4) 4
genomics (4) 4
italy (4) 4
motor-neuron disease (4) 4
research (4) 4
chromosomes (3) 3
degeneration (3) 3
deoxyribonucleic acid--dna (3) 3
development and progression (3) 3
disease (3) 3
frontotemporal dementia (3) 3
gene frequency (3) 3
genetic research (3) 3
genome-wide association study (3) 3
haplotypes (3) 3
internal medicine (3) 3
linkage disequilibrium (3) 3
medical colleges (3) 3
molecular genetics (3) 3
multidisciplinary sciences (3) 3
mutation (3) 3
mutation - genetics (3) 3
polymorphism, single nucleotide - genetics (3) 3
proteins (3) 3
risk factors (3) 3
tdp-43 (3) 3
amyotrophic lateral sclerosis - physiopathology (2) 2
association (2) 2
biochemistry & molecular biology (2) 2
brain - pathology (2) 2
chromosome mapping (2) 2
chromosomes, human, pair 7 (2) 2
chromosomes, human, pair 9 - genetics (2) 2
diagnosis (2) 2
dipeptidyl-peptidases and tripeptidyl-peptidases (2) 2
dna mutational analysis - methods (2) 2
dna-binding proteins - genetics (2) 2
exons - genetics (2) 2
expression (2) 2
gene (2) 2
genetic predisposition to disease - genetics (2) 2
genetic testing (2) 2
genetic variation (2) 2
genetics (2) 2
genetics, population (2) 2
genome, human (2) 2
genomes (2) 2
genotype & phenotype (2) 2
geriatrics & gerontology (2) 2
human genome (2) 2
likelihood functions (2) 2
nerve tissue proteins - genetics (2) 2
neurons (2) 2
neuroscience (2) 2
patients (2) 2
pedigree (2) 2
peptide hydrolases - genetics (2) 2
physiological aspects (2) 2
polymorphisms (2) 2
population genetics (2) 2
potassium channels - genetics (2) 2
prevalence (2) 2
properties (2) 2
protein (2) 2
quantitative trait loci (2) 2
reference values (2) 2
research article (2) 2
sporadic als (2) 2
superoxide dismutase - genetics (2) 2
superoxide dismutase-1 (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Renton, Alan E and Majounie, Elisa and Waite, Adrian and Simón-Sánchez, Javier and Rollinson, Sara and Gibbs, J. Raphael and Schymick, Jennifer C and Laaksovirta, Hannu and van Swieten, John C and Myllykangas, Liisa and Kalimo, Hannu and Paetau, Anders and Abramzon, Yevgeniya and Remes, Anne M and Kaganovich, Alice and Scholz, Sonja W and Duckworth, Jamie and Ding, Jinhui and Harmer, Daniel W and Hernandez, Dena G and Johnson, Janel O and Mok, Kin and Ryten, Mina and Trabzuni, Danyah and Guerreiro, Rita J and Orrell, Richard W and Neal, James and Murray, Alex and Pearson, Justin and Jansen, Iris E and Sondervan, David and Seelaar, Harro and Blake, Derek and Young, Kate and Halliwell, Nicola and Callister, Janis Bennion and Toulson, Greg and Richardson, Anna and Gerhard, Alex and Snowden, Julie and Mann, David and Neary, David and Nalls, Michael A and Peuralinna, Terhi and Jansson, Lilja and Isoviita, Veli-Matti and Kaivorinne, Anna-Lotta and Hölttä-Vuori, Maarit and Ikonen, Elina and Sulkava, Raimo and Benatar, Michael and Wuu, Joanne and Chiò, Adriano and Restagno, Gabriella and Borghero, Giuseppe and Sabatelli, Mario and Heckerman, David and Rogaeva, Ekaterina and Zinman, Lorne and Rothstein, Jeffrey D and Sendtner, Michael and Drepper, Carsten and Eichler, Evan E and Alkan, Can and Abdullaev, Ziedulla and Pack, Svetlana D and Dutra, Amalia and Pak, Evgenia and Hardy, John and Singleton, Andrew and Williams, Nigel M and Heutink, Peter and Pickering-Brown, Stuart and Morris, Huw R and Tienari, Pentti J and Traynor, Bryan J and ITALSGEN Consortium
Neuron, ISSN 0896-6273, 10/2011, Volume 72, Issue 2, pp. 257 - 268
Journal Article
Neuron, ISSN 0896-6273, 12/2010, Volume 68, Issue 5, pp. 857 - 864
Journal Article
Journal Article
Journal Article
Journal Article
Alzheimer's Research & Therapy, ISSN 1758-9193, 07/2012, Volume 4, Issue 30
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized clinically by rapidly progressive paralysis leading ultimately to death... 
Gene mutations | Development and progression | Amyotrophic lateral sclerosis | Genetic aspects | Open reading frames | Properties | Frontotemporal dementia | Health aspects
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 4/2009, Volume 18, Issue 8, pp. 1524 - 1532
The cause of sporadic amyotrophic lateral sclerosis (ALS) is largely unknown, but genetic factors are thought to play a significant role in determining... 
POPULATION | GENETICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PROSTATE-CANCER | SUSCEPTIBILITY | DISEASE | GENES | GENETICS & HEREDITY | ALS | VETERANS | MUTATIONS | Genome-Wide Association Study | Polymorphism, Single Nucleotide | Genome, Human | Amyotrophic Lateral Sclerosis - genetics | Humans | Case-Control Studies | Association Studies
Journal Article
Journal Article