X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (130) 130
Publication (54) 54
Book Review (8) 8
Book Chapter (2) 2
Newspaper Article (2) 2
Conference Proceeding (1) 1
Dissertation (1) 1
Trade Publication Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (84) 84
humans (80) 80
male (57) 57
middle aged (57) 57
female (55) 55
aged (51) 51
clinical neurology (51) 51
article (44) 44
amyotrophic lateral sclerosis (43) 43
neurosciences (40) 40
frontotemporal lobar degeneration (29) 29
adult (28) 28
dementia (28) 28
als (27) 27
amyotrophic-lateral-sclerosis (24) 24
frontotemporal dementia (24) 24
pathology (24) 24
amyotrophic lateral sclerosis - genetics (23) 23
diagnosis (23) 23
aged, 80 and over (22) 22
abridged index medicus (21) 21
amyotrophic lateral sclerosis - pathology (21) 21
neurology (20) 20
tdp-43 (20) 20
brain - pathology (17) 17
alzheimers-disease (16) 16
biomarkers (15) 15
dna-binding proteins - metabolism (15) 15
alzheimer's disease (14) 14
cohort studies (14) 14
motor-neuron disease (14) 14
amyotrophic lateral sclerosis - physiopathology (13) 13
diagnostic-criteria (13) 13
nervous system diseases (13) 13
cognitive impairment (12) 12
criteria (12) 12
mental disorders (12) 12
neurodegenerative diseases (12) 12
research (12) 12
amyotrophic lateral sclerosis - complications (11) 11
brain (11) 11
case-control studies (11) 11
disease (11) 11
disease progression (11) 11
hexanucleotide repeat (11) 11
magnetic resonance imaging (11) 11
medicine & public health (11) 11
proteins (11) 11
proteins - genetics (11) 11
brain - metabolism (10) 10
c9orf72 protein (10) 10
mutation (10) 10
neuropsychological tests (10) 10
age of onset (9) 9
c9orf72 (9) 9
degeneration (9) 9
dna-binding proteins - genetics (9) 9
frontotemporal lobar degeneration - genetics (9) 9
genotype (9) 9
medical colleges (9) 9
neurons (9) 9
amyotrophic lateral sclerosis - diagnosis (8) 8
amyotrophic lateral sclerosis - metabolism (8) 8
amyotrophic lateral sclerosis - psychology (8) 8
cross-sectional studies (8) 8
motor neurons - pathology (8) 8
mutations (8) 8
neurodegeneration (8) 8
ophthalmology (8) 8
retrospective studies (8) 8
sclerosis (8) 8
young adult (8) 8
analysis (7) 7
biomarker (7) 7
cerebrospinal fluid (7) 7
cognition disorders - etiology (7) 7
genetic predisposition to disease (7) 7
genetics (7) 7
longitudinal studies (7) 7
medical research (7) 7
motor neuron disease (7) 7
mutation - genetics (7) 7
nutritional and metabolic diseases (7) 7
parkinson's disease (7) 7
protein binding (7) 7
tau (7) 7
adolescent (6) 6
alpha-synuclein (6) 6
amyotrophic lateral sclerosis - epidemiology (6) 6
dementia - pathology (6) 6
dna (6) 6
genetic aspects (6) 6
immunohistochemistry (6) 6
lobar degeneration (6) 6
medicine, experimental (6) 6
motor neurons - metabolism (6) 6
nervous system (6) 6
neuroimaging (6) 6
neuropathology (6) 6
physiological aspects (6) 6
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Lancet Neurology, The, ISSN 1474-4422, 2008, Volume 7, Issue 5, pp. 409 - 416
Journal Article
Annals of Neurology, ISSN 0364-5134, 07/2013, Volume 74, Issue 1, pp. 20 - 38
Journal Article
Nature, ISSN 0028-0836, 08/2010, Volume 466, Issue 7310, pp. 1069 - 1075
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 9/2014, Volume 128, Issue 3, pp. 423 - 437
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2011, Volume 108, Issue 52, pp. 20881 - 20890
Amyotrophic lateral sclerosis (ALS) is a devastating and universally fatal neurodegenerative disease. Mutations in two related RNA-binding proteins, TDP-43 and... 
Aggregation | Proteins | Yeasts | Nervous system diseases | Neurodegenerative diseases | Neurons | Drosophila | Prions | Amyotrophic lateral sclerosis | Genetic mutation | WILD-TYPE | TDP-43 PROTEINOPATHY | DROSOPHILA MODEL | MULTIDISCIPLINARY SCIENCES | NEURODEGENERATION | AMYLOID PORES | TOXICITY | AMYOTROPHIC-LATERAL-SCLEROSIS | FUS MUTATIONS | FRONTOTEMPORAL LOBAR DEGENERATION | AGGREGATION | Immunohistochemistry | Protein Structure, Tertiary | RNA-Binding Proteins - genetics | TATA-Binding Protein Associated Factors - metabolism | Saccharomyces cerevisiae - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Cells, Cultured | Computational Biology | Genetic Association Studies - methods | TATA-Binding Protein Associated Factors - genetics | Drosophila melanogaster - genetics | Mutation, Missense - genetics | Motor Neurons - metabolism | Animals | Spinal Cord - cytology | Yeast fungi | Gene mutations | Physiological aspects | Development and progression | Genetic aspects | Research | Binding proteins | Health aspects | Yeast | Ribonucleic acid--RNA | Genes | Index Medicus | Motor neurons | FUS protein | RNA-binding protein | Spinal cord | RNA | Mutation | Bioinformatics | Biological Sciences | amyotrophic-lateral-sclerosis; frontotemporal lobar degeneration; drosophila model; fus mutations; tdp-43 proteinopathy; amyloid pores; wild-type; toxicity; neurodegeneration; aggregation | Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
by van Rheenen, Wouter and Shatunov, Aleksey and Dekker, Annelot M and McLaughlin, Russell L and Diekstra, Frank P and Pulit, Sara L and van der Spek, Rick A. A and Võsa, Urmo and de Jong, Simone and Robinson, Matthew R and Yang, Jian and Fogh, Isabella and van Doormaal, Perry Tc and Tazelaar, Gijs H. P and Koppers, Max and Blokhuis, Anna M and Sproviero, William and Jones, Ashley R and Kenna, Kevin P and van Eijk, Kristel R and Harschnitz, Oliver and Schellevis, Raymond D and Brands, William J and Medic, Jelena and Menelaou, Anoniki and Vajda, Alice and Ticozzi, Nicola and Lin, Kuang and Rogelj, Boris and Vrabec, Katarina and Ravnik-Glavač, Metka and Koritnik, Blaž and Zidar, Janez and Leonardis, Lea and Grošelj, Leja Dolenc and Millecamps, Stéphanie and Salachas, François and Meininger, Vincent and de Carvalho, Mamede and Pinto, Susana and Mora, Jesus S and Rojas-García, Ricardo and Polak, Meraida and Chanan, Siddharthan and Colville, Shuna and Swingler, Robert and Morrison, Karen E and Shaw, Pamela J and Hardy, John and Orrell, Richard W and Pittman, Alan and Sidle, Katie and Fratta, Pietro and Malaspina, Anea and Topp, Simon and Petri, Susanne and Abdulla, Susanne and pper, Carsten and Sendtner, Michael and Meyer, Thomas and Ophoff, Roel A and Staats, Kim A and Wiedau-Pazos, Martina and Lomen-Hoerth, Catherine and van Deerlin, Vivianna M and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Basak, A. Nazli and Tunca, Ceren and Hamzeiy, Hamid and Parman, Yesim and Meitinger, Thomas and Lichtner, Peter and Radivojkov-Blagojevic, Milena and Anes, Christian R and Maurel, Cindy and Bensimon, Gilbert and Landwehrmeyer, Bernhard and Brice, Alexis and Payan, Christine A. M and Saker-Delye, Safaa and Dürr, Alexana and Wood, Nicholas W and Tittmann, Lukas and Lieb, Wolfgang and Franke, Ane and Rietschel, Marcella and Cichon, Sven and Nöthen, Markus M and Amouyel, Philippe and Tzourio, Christophe and Dartigues, Jean-François and Uitterlinden, Ane G and Rivadeneira, Fernando and Estrada, Karol and Hofman, Albert and Curtis, Charles and Blauw, Hylke M and van der Kooi, Anneke J and ... and PARALS Registry and FALS Sequencing Consortium and SLALOM Grp and SLAGEN Consortium and NNIPPS Study Grp and SLAP Registry and SLALOM Group and NNIPPS Study Group 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. 1043 - 1048
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 6/2012, Volume 123, Issue 6, pp. 825 - 839
C9ORF72-hexanucleotide repeat expansions and ubiquilin-2 (UBQLN2) mutations are recently identified genetic markers in amyotrophic lateral sclerosis (ALS) and... 
Pathology | Neurosciences | Medicine & Public Health | UBQLN1 | Amyotrophic lateral sclerosis | Frontotemporal lobar degeneration | C9ORF72 | UBQLN2 | DNA-BINDING | REPEAT EXPANSION | PROTEIN | ALZHEIMERS-DISEASE | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | TDP-43 PROTEINOPATHIES | MUTATIONS | DIAGNOSTIC-CRITERIA | SUPEROXIDE-DISMUTASE | Frontotemporal Lobar Degeneration - pathology | Ubiquitins - genetics | Humans | Middle Aged | Male | DNA-Binding Proteins - metabolism | DNA Repeat Expansion | Frontotemporal Lobar Degeneration - mortality | Aged, 80 and over | Cell Cycle Proteins - genetics | Female | C9orf72 Protein | Ubiquitins - metabolism | Amyotrophic Lateral Sclerosis - genetics | Cell Cycle Proteins - metabolism | DNA-Binding Proteins - genetics | Mutation - genetics | Amyotrophic Lateral Sclerosis - mortality | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Proteins - metabolism | Age of Onset | Amyotrophic Lateral Sclerosis - metabolism | Inclusion Bodies - pathology | Aged | Frontotemporal Lobar Degeneration - genetics | Index Medicus | Cerebellum | Immunohistochemistry | Spinal cord | Prognosis | Neurodegenerative diseases | Neuropathology | Antibodies | Data processing | Axons | Genetic markers | Inclusion bodies | Genetic analysis | Mutation | Frontotemporal dementia | Hippocampus
Journal Article
Journal Article