X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (94) 94
index medicus (92) 92
article (63) 63
neurosciences (57) 57
amyotrophic lateral sclerosis - genetics (54) 54
male (53) 53
middle aged (51) 51
amyotrophic lateral sclerosis (49) 49
clinical neurology (45) 45
female (45) 45
aged (44) 44
adult (33) 33
neurology (33) 33
als (31) 31
genetic aspects (29) 29
amyotrophic-lateral-sclerosis (28) 28
dementia (28) 28
frontotemporal dementia (27) 27
mutations (25) 25
internal medicine (21) 21
aged, 80 and over (20) 20
analysis (20) 20
c9orf72 protein (20) 20
genes (20) 20
genetic predisposition to disease (20) 20
genetics (20) 20
mutation (20) 20
proteins - genetics (20) 20
c9orf72 (19) 19
cohort studies (19) 19
geriatrics & gerontology (19) 19
natural sciences (19) 19
naturvetenskap (19) 19
research (19) 19
case-control studies (18) 18
genome-wide association study (18) 18
polymorphism, single nucleotide (18) 18
risk factors (18) 18
disease (17) 17
experiment (17) 17
fysik (17) 17
genetics & heredity (17) 17
genomes (17) 17
genotype (17) 17
mutation - genetics (17) 17
particle physics (17) 17
physical sciences (17) 17
frontotemporal dementia - genetics (16) 16
genetic predisposition to disease - genetics (16) 16
genomics (16) 16
high energy physics - experiment (16) 16
physics (16) 16
frontotemporal lobar degeneration (15) 15
genetic research (15) 15
phenotype (15) 15
physics - high energy physics - experiment (15) 15
population (15) 15
polymorphism, single nucleotide - genetics (14) 14
young adult (14) 14
abridged index medicus (13) 13
amyotrophic lateral sclerosis - pathology (13) 13
gene (13) 13
genome-wide association (13) 13
physics, particles & fields (13) 13
susceptibility (13) 13
association (12) 12
pedigree (12) 12
adolescent (11) 11
alleles (11) 11
biochemistry & molecular biology (11) 11
brain (11) 11
gene expression (11) 11
hexanucleotide repeat (11) 11
medical research (11) 11
neurodegeneration (11) 11
parkinson disease - genetics (11) 11
physics of elementary particles and fields (11) 11
tdp-43 (11) 11
alzheimers-disease (10) 10
animals (10) 10
diagnosis (10) 10
dna-binding proteins - genetics (10) 10
mental disorders (10) 10
molecular genetics (10) 10
nervous system diseases (10) 10
protein (10) 10
risk (10) 10
age of onset (9) 9
amyotrophic lateral sclerosis - epidemiology (9) 9
detectors (9) 9
ftd (9) 9
genetic variation (9) 9
hexanucleotide repeat expansion (9) 9
high energy physics (9) 9
parkinson's disease (9) 9
subatomic physics (9) 9
subatomär fysik (9) 9
chromosomes, human, pair 9 - genetics (8) 8
dna repeat expansion (8) 8
heterozygote (8) 8
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


Lancet Neurology, The, ISSN 1474-4422, 2010, Volume 9, Issue 10, pp. 986 - 994
Journal Article
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2015, Volume 43, pp. 180.e1 - 180.e5
Journal Article
Physical Medicine and Rehabilitation Clinics of North America, ISSN 1047-9651, 08/2008, Volume 19, Issue 3, pp. 461 - 477
Journal Article
by Majounie, Elisa, PhD and Renton, Alan E, PhD and Mok, Kin, MSc and Dopper, Elise GP and Waite, Adrian, PhD and Rollinson, Sara, PhD and Chiò, Adriano, MD and Restagno, Gabriella, MD and Nicolaou, Nayia, MSc and Simon-Sanchez, Javier, PhD and van Swieten, John C, Prof and Abramzon, Yevgeniya and Johnson, Janel O, PhD and Sendtner, Michael, Prof and Pamphlett, Roger, MD and Orrell, Richard W, MD and Mead, Simon, MD and Sidle, Katie C, MD and Houlden, Henry, Prof and Rohrer, Jonathan D, MD and Morrison, Karen E, Prof and Pall, Hardev, MD and Talbot, Kevin, Prof and Ansorge, Olaf, MD and Hernandez, Dena G, MSc and Arepalli, Sampath, MS and Sabatelli, Mario, MD and Mora, Gabriele, MD and Corbo, Massimo, MD and Giannini, Fabio, MD and Calvo, Andrea, MD and Englund, Elisabet, MD and Borghero, Giuseppe, MD and Floris, Gian Luca, MD and Remes, Anne M, Prof and Laaksovirta, Hannu, MD and McCluskey, Leo, MD and Trojanowski, John Q, Prof and Van Deerlin, Vivianna M, MD and Schellenberg, Gerard D, Prof and Nalls, Michael A, PhD and Drory, Vivian E, MD and Lu, Chin-Song, Prof and Yeh, Tu-Hsueh, MD and Ishiura, Hiroyuki, MD and Takahashi, Yuji, MD and Tsuji, Shoji, Prof and Le Ber, Isabelle, MD and Brice, Alexis, Prof and Drepper, Carsten, PhD and Williams, Nigel, PhD and Kirby, Janine, PhD and Shaw, Pamela, Prof and Hardy, John, Prof and Tienari, Pentti J, MD and Heutink, Peter, Prof and Morris, Huw R, MD and Pickering-Brown, Stuart, Prof and Traynor, Bryan J, Dr and Chromosome 9-ALS FTD Consortium and French Res Network FTLD FTLD ALS and ITALSGEN Consortium and French research network on FTLD/FTLD/ALS and Chromosome 9-ALS/FTD Consortium and Oncology and Pathology, Kamprad Lab and Lund University and Lunds universitet and Onkologi och Patologi, Kampradlab
Lancet Neurology, The, ISSN 1474-4422, 2012, Volume 11, Issue 4, pp. 323 - 330
Summary Background We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9orf72 that has been associated with a large... 
Neurology | PREVALENCE | MUTATIONS | LOBAR DEGENERATION | GENETICS | TDP-43 | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Cross-Sectional Studies | DNA Repeat Expansion - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Child, Preschool | Genotype | Male | Genetic Loci | Open Reading Frames - genetics | Young Adult | Chromosomes, Human, Pair 9 - genetics | Adolescent | Age of Onset | Aged, 80 and over | Adult | Female | Aged | Child | Cohort Studies | Medical research | Medical colleges | Care and treatment | Nervous system diseases | Neurosciences | Molecular genetics | Oncology, Experimental | Questions and answers | Amyotrophic lateral sclerosis | Research | Medicine, Experimental | Agriculture | Physicians (General practice) | Alzheimer's disease | Dementia | Cancer | Biomedical engineering | Haplotypes | Polymerase chain reaction | Neurodegenerative diseases | Ethnic groups | Data processing | Mutation | Frontotemporal dementia | Genetic counselling | Islands | Age | Toll-Like Receptor 4 | Open Reading Frames | Adaptor Proteins, Vesicular Transport | Lipopolysaccharides | Life Sciences | DNA Repeat Expansion | Interferon Regulatory Factor-3 | Transfection | Amyotrophic Lateral Sclerosis | RNA Interference | HEK293 Cells | Membrane Glycoproteins | Vesicular Transport Proteins | Protein Structure, Tertiary | Cell Line | Chemokine CCL5 | Frontotemporal Dementia | Signal Transduction | Myeloid Differentiation Factor 88 | Chromosomes, Human, Pair 9 | Protein Transport | Adaptor Proteins, Signal Transducing | Santé publique et épidémiologie | RNA, Small Interfering | Endosomes | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article
Lancet Oncology, The, ISSN 1470-2045, 2010, Volume 11, Issue 10, pp. 962 - 972
Journal Article
Journal Article
by Anttila, Verneri and Winsvold, Bendik S and Gormley, Padhraig and Kurth, Tobias and Bettella, Francesco and McMahon, George and Kallela, Mikko and Malik, Rainer and de Vries, Boukje and Terwindt, Gisela and Medland, Sarah E and Todt, Unda and McArdle, Wendy L and Quaye, Lydia and Koiranen, Markku and Ikram, M. Arfan and Lehtimaki, Terho and Stam, Anine H and Ligthart, Lannie and Wedenoja, Juho and Dunham, Ian and Neale, Benjamin M and Palta, Priit and Hamalainen, Eija and Schuerks, Markus and Rose, Lynda M and Buring, Julie E and Ridker, Paul M and Steinberg, Stacy and Stefansson, Hreinn and Jakobsson, Finnbogi and Lawlor, Debbie A and Evans, David M and Ring, Susan M and Farkkila, Markus and Artto, Ville and Kaunisto, Mari A and Freilinger, Tobias and Schoenen, Jean and Frants, Rune R and Pelzer, Nadine and Weller, Claudia M and Zielman, Ronald and Heath, Anew C and Madden, Pamela A. F and Montgomery, Grant W and Martin, Nicholas G and Borck, Guntram and Goebel, Hartmut and Heinze, Axel and Heinze-Kuhn, Katja and Williams, Frances M. K and Hartikainen, Anna-Liisa and Pouta, Anneli and van den Ende, Joyce and Uitterlinden, Ane G and Hofman, Albert and Amin, Najaf and Hottenga, Jouke-Jan and Vink, Jacqueline M and Heikkila, Kauko and Alexander, Michael and Muller-Myhsok, Bertram and Schreiber, Stefan and Meitinger, Thomas and Wichmann, Heinz Erich and Aromaa, Arpo and Eriksson, Johan G and Traynor, Bryan J and Trabzuni, Daniah and Rossin, Elizabeth and Lage, Kasper and Jacobs, Suzanne B. R and Gibbs, J. Raphael and Birney, Ewan and Kaprio, Jaakko and Penninx, Brenda W and Boomsma, Dorret I and van Duijn, Cornelia and Raitakari, Olli and Jarvelin, Marjo-Riitta and Zwart, John-Anker and Cherkas, Lynn and Strachan, David P and Kubisch, Christian and Ferrari, Michel D and van den Maagdenberg, Arn M. J. M and Dichgans, Martin and Wessman, Maija and Smith, George Davey and Stefansson, Kari and Daly, Mark J and Nyholt, Dale R and Chasman, Daniel I and Palotie, Aarno and UK Brain Expression Consortium and Int Headache Genetics Consortium and North Amer Brain Expression and the International Headache Genetics Consortium and North American Brain Expression Consortium
Nature Genetics, ISSN 1061-4036, 08/2013, Volume 45, Issue 8, pp. 912 - U255
Migraine is the most common brain disorder, affecting approximately 14% of the adult population, but its molecular mechanisms are poorly understood. We report... 
PROTEIN | LEWIS(X) | GENES | GENETICS & HEREDITY | DOWN-REGULATION | TRANSFORMING-GROWTH-FACTOR | MUTATIONS | ASSOCIATION | EXPRESSION | FAMILY | Genetic susceptibility | Genetic variation | Migraine | Physiological aspects | Genetic aspects | Research | Risk factors | Studies | Proteins | Signal transduction | Headaches | Population | Genomes | Meta-analysis
Journal Article
Neuron, ISSN 0896-6273, 09/2014, Volume 83, Issue 5, pp. 1043 - 1050
Journal Article