X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (57) 57
humans (55) 55
amyotrophic lateral sclerosis - genetics (37) 37
amyotrophic lateral sclerosis (36) 36
female (35) 35
male (35) 35
neurosciences (32) 32
middle aged (29) 29
article (27) 27
aged (26) 26
clinical neurology (26) 26
hexanucleotide repeat (25) 25
amyotrophic-lateral-sclerosis (23) 23
als (22) 22
proteins - genetics (22) 22
c9orf72 protein (21) 21
frontotemporal dementia (21) 21
mutation (21) 21
genetic aspects (20) 20
frontotemporal dementia - genetics (19) 19
frontotemporal lobar degeneration (18) 18
c9orf72 (17) 17
dementia (17) 17
neurology (16) 16
adult (15) 15
cohort studies (15) 15
proteins (15) 15
aged, 80 and over (14) 14
mutation - genetics (14) 14
genetics (13) 13
pathology (13) 13
genes (12) 12
mutations (12) 12
dna repeat expansion - genetics (11) 11
amyotrophic lateral sclerosis - pathology (10) 10
dna repeat expansion (10) 10
ftd (10) 10
motor neuron disease (10) 10
analysis (9) 9
animals (9) 9
disease (9) 9
geriatrics & gerontology (9) 9
internal medicine (9) 9
motor neuron disease - genetics (9) 9
neurodegeneration (9) 9
expansion (8) 8
genetic predisposition to disease (8) 8
genetic predisposition to disease - genetics (8) 8
genetic research (8) 8
genetics & heredity (8) 8
genomes (8) 8
genotype (8) 8
medicine & public health (8) 8
nervous system diseases (8) 8
risk factors (8) 8
age of onset (7) 7
brain - metabolism (7) 7
brain - pathology (7) 7
dna mutational analysis (7) 7
frontotemporal dementia - metabolism (7) 7
gene (7) 7
gene expression (7) 7
heterozygote (7) 7
nervous system (7) 7
neurodegenerative diseases (7) 7
rna (7) 7
tdp-43 (7) 7
abridged index medicus (6) 6
aging (6) 6
amyotrophic lateral sclerosis - metabolism (6) 6
case-control studies (6) 6
cerebellum - metabolism (6) 6
degeneration (6) 6
dna-binding proteins - genetics (6) 6
familial als (6) 6
frontal lobe - metabolism (6) 6
frontotemporal lobar degeneration - genetics (6) 6
genomics (6) 6
mental disorders (6) 6
polymerase chain reaction (6) 6
protein binding (6) 6
rna foci (6) 6
rna, messenger - metabolism (6) 6
alzheimer's disease (5) 5
brain (5) 5
c9orf72 protein - genetics (5) 5
development and progression (5) 5
frontotemporal dementia - pathology (5) 5
genetic association studies (5) 5
identification (5) 5
mice (5) 5
multidisciplinary sciences (5) 5
parkinson disease - genetics (5) 5
parkinson's disease (5) 5
pathogenesis (5) 5
pedigree (5) 5
phenotype (5) 5
protein (5) 5
repeat expansion (5) 5
research (5) 5
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 477 - 478
Noncoding expanded repeats have been implicated in a wide range of diseases. A new report uncovers expanded TTTCA and TTTTA repeats in an intronic region of... 
LOCALIZATION | GENE | DISEASE | GENETICS & HEREDITY | ALS | NEURODEGENERATION | TRANSLATION | Adult | Introns | Humans | Epilepsies, Myoclonic - genetics | Seizures | Psychological aspects | Myoclonic epilepsy | Care and treatment | Adults | Genetic aspects | Research | Chromosomes
Journal Article
Nature reviews. Neurology, ISSN 1759-4758, 02/2013, Volume 9, Issue 2, pp. 63 - 64
Journal Article
Nature Genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 477 - 478
Noncoding expanded repeats have been implicated in a wide range of diseases. A new report uncovers expanded TTTCA and TTTTA repeats in an intronic region of... 
Proteins | Disease | Epilepsy | Genomes | Chromosomes
Journal Article
NATURE REVIEWS NEUROLOGY, ISSN 1759-4758, 12/2015, Volume 11, Issue 12, pp. 670 - 672
The molecular mechanisms of neurodegeneration due to a repeat expansion in C9orf72, the most common cause of frontotemporal dementia and amyotrophic lateral... 
EXPANSION | FTD | ALS | TOXICITY | AMYOTROPHIC-LATERAL-SCLEROSIS | HEXANUCLEOTIDE REPEAT | CLINICAL NEUROLOGY | Molecular targeted therapy | Nervous system | Development and progression | Degeneration | Genetic aspects | Open reading frames | Health aspects | Methods
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 12/2013, Volume 126, Issue 6, pp. 829 - 844
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 2015, Volume 130, Issue 1, pp. 77 - 92
Journal Article
Neuron, ISSN 0896-6273, 10/2014, Volume 84, Issue 2, pp. 241 - 243
Identifying disease genes implicated in late-onset neurodegenerative disorders can be challenging due to the lack of DNA samples from multiple affected family... 
FTD | EXPANSION | AMYOTROPHIC-LATERAL-SCLEROSIS | MUTATIONS | HEXANUCLEOTIDE REPEAT | C9ORF72 | NEUROSCIENCES | Tubulin - genetics | Exome - genetics | Genetic Predisposition to Disease | Mutation - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Amyotrophic lateral sclerosis | Nervous system diseases | Analysis
Journal Article
Nature Neuroscience, ISSN 1097-6256, 08/2015, Volume 18, Issue 8, pp. 1175 - 1182
Journal Article
Nature Reviews Neurology, ISSN 1759-4758, 02/2013, Volume 9, Issue 2, pp. 63 - 64
In 2012, researchers published extensively on the genetic and clinicopathological characterization of patients with the newly discovered C90RF72 repeat... 
FRONTOTEMPORAL DEMENTIA | EXPANSION | FTD | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | HEXANUCLEOTIDE REPEAT | C9ORF72 | CLINICAL NEUROLOGY | Amyotrophic lateral sclerosis | Genetic aspects | Research | Gene expression | Risk factors
Journal Article
Journal Article
by Kenna, Kevin P and van Doormaal, Perry T. C and Dekker, Annelot M and Ticozzi, Nicola and Kenna, Brendan J and Diekstra, Frank P and van Rheenen, Wouter and van Eijk, Kristel R and Jones, Ashley R and Keagle, Pamela and Shatunov, Aleksey and Sproviero, William and Smith, Bradley N and van Es, Michael A and Topp, Simon D and Kenna, Aoife and Miller, Jack W and Fallini, Claudia and Tiloca, Cinzia and McLaughlin, Russell L and Vance, Caroline and Troakes, Claire and Colombrita, Claudia and Mora, Gabriele and Calvo, Anea and Verde, Federico and Al-Sarraj, Safa and King, Anew and Calini, Daniela and de Belleroche, Jacqueline and Baas, Frank and van der Kooi, Anneke J and de Visser, Marianne and ten Asbroek, Anneloor L. M. A and Sapp, Peter C and McKenna-Yasek, Diane and Polak, Meraida and Asress, Seneshaw and Muñoz-Blanco, José Luis and Strom, Tim M and Meitinger, Thomas and Morrison, Karen E and Lauria, Giuseppe and Williams, Kelly L and Leigh, P. Nigel and Nicholson, Garth A and Blair, Ian P and Leblond, Claire S and Dion, Patrick A and Rouleau, Guy A and Pall, Hardev and Shaw, Pamela J and Turner, Martin R and Talbot, Kevin and Taroni, Franco and Boylan, Kevin B and van Blitterswijk, Marka and Rademakers, Rosa and Esteban-Pérez, Jesús and García-Redondo, Alberto and van Damme, Phillip and Robberecht, Wim and Chio, Aiano and Gellera, Cinzia and pper, Carsten and Sendtner, Michael and Ratti, Antonia and Glass, Jonathan D and Mora, Jesús S and Basak, Nazli A and Hardiman, Orla and Ludolph, Albert C and Andersen, Peter M and Weishaupt, Jochen H and Brown, Robert H and Al-Chalabi, Ammar and Silani, Vincenzo and Shaw, Christopher E and van den Berg, Leonard H and Veldink, Jan H and Landers, John E and D'alfonso, Sana and Mazzini, Letizia and Comi, Giacomo P and del Bo, Roberto and Ceroni, Mauro and Gagliardi, Stella and Querin, Giorgia and Bertolin, Cinzia and Pensato, Viviana and Castellotti, Barbara and Corti, Stefania and Cereda, Cristina and Corrado, Lucia and Sorarù, Gianni and SLAGEN Consortium and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk neurovetenskap and Umeå universitet
Nature genetics, ISSN 1061-4036, 2016, Volume 48, Issue 9, pp. 1037 - 1042
Journal Article