X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (44) 44
neurosciences (32) 32
index medicus (30) 30
frontotemporal dementia (29) 29
male (29) 29
clinical neurology (27) 27
female (26) 26
dementia (24) 24
middle aged (23) 23
aged (19) 19
mutation (18) 18
article (17) 17
neurology (16) 16
frontotemporal dementia - genetics (15) 15
risk factors (14) 14
genetic aspects (13) 13
genetic predisposition to disease (13) 13
lobar degeneration (13) 13
tau (13) 13
adult (11) 11
aged, 80 and over (11) 11
analysis (11) 11
genetic research (11) 11
mental disorders (11) 11
dementia - genetics (10) 10
internal medicine (10) 10
mutations (10) 10
age of onset (9) 9
amyotrophic-lateral-sclerosis (9) 9
frontotemporal lobar degeneration (9) 9
genes (9) 9
geriatrics & gerontology (9) 9
polymorphism, single nucleotide (9) 9
progressive supranuclear palsy (9) 9
tau proteins - genetics (9) 9
alzheimer's disease (8) 8
disease (8) 8
gene expression (8) 8
genome-wide association study (8) 8
genomics (8) 8
genotype (8) 8
pathology (8) 8
aging (7) 7
alzheimer disease - genetics (7) 7
alzheimers-disease (7) 7
association (7) 7
genetic predisposition to disease - genetics (7) 7
genomes (7) 7
haplotypes (7) 7
intercellular signaling peptides and proteins - genetics (7) 7
pedigree (7) 7
prevalence (7) 7
amyotrophic lateral sclerosis (6) 6
brain (6) 6
cohort studies (6) 6
dementia disorders (6) 6
ftd (6) 6
gene (6) 6
genome-wide association (6) 6
hexanucleotide repeat (6) 6
mutation - genetics (6) 6
neurodegeneration (6) 6
research (6) 6
als (5) 5
animals (5) 5
brain - pathology (5) 5
c9orf72 (5) 5
common variants (5) 5
consensus (5) 5
diagnosis (5) 5
exons - genetics (5) 5
frontotemporal dementia - epidemiology (5) 5
genetics (5) 5
mapt (5) 5
medical colleges (5) 5
nervous system diseases (5) 5
neurodegenerative diseases (5) 5
parkinsons-disease (5) 5
patients (5) 5
phenotype (5) 5
polymorphism, single nucleotide - genetics (5) 5
protein (5) 5
tdp-43 (5) 5
age (4) 4
alleles (4) 4
care and treatment (4) 4
case-control studies (4) 4
diagnostic-criteria (4) 4
dna mutational analysis (4) 4
frontotemporal dementia - diagnosis (4) 4
frontotemporal dementia - pathology (4) 4
fus (4) 4
medicine (4) 4
molecular sequence data (4) 4
nervous system (4) 4
neurons (4) 4
neuropathology (4) 4
nutritional and metabolic diseases (4) 4
proteins (4) 4
psychiatry (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


by Ferrari, Raffaele, PhD and Hernandez, Dena G, MSc and Nalls, Michael A, PhD and Rohrer, Jonathan D, PhD and Ramasamy, Adaikalavan, PhD and Kwok, John B J, PhD and Dobson-Stone, Carol, PhD and Brooks, William S, MBBS and Schofield, Peter R, Prof and Halliday, Glenda M, Prof and Hodges, John R, Prof and Piguet, Olivier, PhD and Bartley, Lauren, MSc and Thompson, Elizabeth, MD and Haan, Eric, Prof and Hernández, Isabel, MD and Ruiz, Agustín, MD and Boada, Mercè, MD and Borroni, Barbara, MD and Padovani, Alessandro, Prof and Cruchaga, Carlos, PhD and Cairns, Nigel J, Prof and Benussi, Luisa, PhD and Binetti, Giuliano, MD and Ghidoni, Roberta, PhD and Forloni, Gianluigi, PhD and Galimberti, Daniela, PhD and Fenoglio, Chiara, PhD and Serpente, Maria, PhD and Scarpini, Elio, MD and Clarimón, Jordi, PhD and Lleó, Alberto, MD and Blesa, Rafael, MD and Waldö, Maria Landqvist, MD and Nilsson, Karin, PhD and Nilsson, Christer, PhD and Mackenzie, Ian R A, Prof and Hsiung, Ging-Yuek R, MD and Mann, David M A, Prof and Grafman, Jordan, Prof and Morris, Christopher M, PhD and Attems, Johannes, Prof and Griffiths, Timothy D, Prof and McKeith, Ian G, Prof and Thomas, Alan J, Prof and Pietrini, P, Prof and Huey, Edward D, MD and Wassermann, Eric M, MD and Baborie, Atik, MD and Jaros, Evelyn, PhD and Tierney, Michael C, MSc and Pastor, Pau, MD and Razquin, Cristina, PhD and Ortega-Cubero, Sara, MD and Alonso, Elena, BSc and Perneczky, Robert, MD and Diehl-Schmid, Janine, MD and Alexopoulos, Panagiotis, MD and Kurz, Alexander, MD and Rainero, Innocenzo, MD and Rubino, Elisa, MD and Pinessi, Lorenzo, Prof and Rogaeva, Ekaterina, PhD and St George-Hyslop, Peter, MD and Rossi, Giacomina, PhD and Tagliavini, Fabrizio, MD and Giaccone, Giorgio, MD and Rowe, James B, PhD and Schlachetzki, Johannes C M, MD and Uphill, James, BSc and Collinge, John, Prof and Mead, Simon, Prof and Danek, Adrian, MD and Van Deerlin, Vivianna M, PhD and Grossman, Murray, Prof and Trojanowski, John Q, Prof and van der Zee, Julie, PhD and Deschamps, William, MSc and Van Langenhove, Tim, MD and Cruts, Marc, PhD and Van Broeckhoven, Christine, Prof and Cappa, Stefano F, Prof and Le Ber, Isabelle, MD and Hannequin, Didier, Prof and Golfier, Véronique, MD and Vercelletto, Martine, MD and Brice, Alexis, MD and Nacmias, Benedetta, PhD and Sorbi, Sandro, Prof and Bagnoli, Silvia, PhD and Piaceri, Irene, PhD and Nielsen, Jørgen E, MD and Hjermind, Lena E, MD and Riemenschneider, Matthias, Prof and Mayhaus, Manuel, PhD and Ibach, Bernd, PhD and Gasparoni, Gilles, PhD and Pichler, Sabrina, MSc and Gu, Wei, PhD and Rossor, Martin N, Prof and ... and Lund University and Psychiatry (Lund) and MultiPark: Multidisciplinary research focused on Parkinson´s disease and Psykiatri, Lund and Lunds universitet
Lancet Neurology, The, ISSN 1474-4422, 2014, Volume 13, Issue 7, pp. 686 - 699
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2007, Volume 6, Issue 10, pp. 857 - 868
Journal Article
Journal of Molecular Neuroscience, ISSN 0895-8696, 11/2011, Volume 45, Issue 3, pp. 500 - 515
Frontotemporal lobar degeneration is the most common cause of dementia of non-Alzheimer's type worldwide. It manifests, clinically, with behavioural changes... 
Neurochemistry | Neurology | Neurosciences | Genome-wide association studies | Biomedicine | Genetic variability | PGRN | Proteomics | MAPT | Frontotemporal dementia | Cell Biology | PROGRANULIN GENE | COMMON VARIANTS | LOBAR DEGENERATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TAU GENE | DEVELOPMENTAL DELAY | NEUROSCIENCES | MAPT GENE | INCLUSION-BODY MYOPATHY | MULTIPLE SYSTEM TAUOPATHY | 17Q21.31 MICRODUPLICATION | PROGRESSIVE SUPRANUCLEAR PALSY | Frontotemporal Dementia - genetics | Frontotemporal Dementia - physiopathology | Haplotypes | Frontotemporal Lobar Degeneration - pathology | Genome-Wide Association Study | Exons | Humans | Valosin Containing Protein | Intercellular Signaling Peptides and Proteins - genetics | Endosomal Sorting Complexes Required for Transport - genetics | Frontotemporal Lobar Degeneration - physiopathology | tau Proteins - genetics | Cell Cycle Proteins - genetics | Adenosine Triphosphatases - genetics | Frontotemporal Lobar Degeneration - genetics | Mutation | Frontotemporal Dementia - pathology | Care and treatment | Genetic research | Genetic aspects | Forecasts and trends | Diagnosis | Methods | Dementia | Brain | Temporal lobe | valosin-containing protein | Sarcoma | Neurons | Nervous system | Genomes | Glial cells | DNA-binding protein | Language | Tau protein | Microtubule-associated proteins | Dementia disorders
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 05/2017, Volume 133, Issue 5, pp. 825 - 837
Journal Article
by Broce, Iris and Karch, Celeste M and Wen, Natalie and Fan, Chun C and Wang, Yunpeng and Hong Tan, Chin and Kouri, Naomi and Ross, Owen A and Höglinger, Günter U and Muller, Ulrich and Hardy, John and Momeni, Parastoo and Hess, Christopher P and Dillon, William P and Miller, Zachary A and Bonham, Luke W and Rabinovici, Gil D and Rosen, Howard J and Schellenberg, Gerard D and Franke, Andre and Karlsen, Tom H and Veldink, Jan H and Ferrari, Raffaele and Yokoyama, Jennifer S and Miller, Bruce L and Andreassen, Ole A and Dale, Anders M and Desikan, Rahul S and Sugrue, Leo P and Ferrari, Raffaele and Hernandez, Dena G and Nalls, Michael A and Rohrer, Jonathan D and Ramasamy, Adaikalavan and Kwok, John B.J and Dobson-Stone, Carol and Brooks, William S and Schofield, Peter R and Halliday, Glenda M and Hodges, John R and Piguet, Olivier and Bartley, Lauren and Thompson, Elizabeth and Haan, Eric and Hernández, Isabel and Ruiz, Agustín and Boada, Mercè and Borroni, Barbara and Padovani, Alessandro and Cruchaga, Carlos and Cairns, Nigel J and Benussi, Luisa and Binetti, Giuliano and Ghidoni, Roberta and Forloni, Gianluigi and Albani, Diego and Galimberti, Daniela and Fenoglio, Chiara and Serpente, Maria and Scarpini, Elio and Clarimón, Jordi and Lleó, Alberto and Blesa, Rafael and Landqvist Waldö, Maria and Nilsson, Karin and Nilsson, Christer and Mackenzie, Ian R.A and Hsiung, Ging-Yuek R and Mann, David M.A and Grafman, Jordan and Morris, Christopher M and Attems, Johannes and Griffiths, Timothy D and G McKeith, Ian and Thomas, Alan J and Pietrini, Pietro and Huey, Edward D and Wassermann, Eric M and Baborie, Atik and Jaros, Evelyn and Tierney, Michael C and Pastor, Pau and Razquin, Cristina and Ortega-Cubero, Sara and Alonso, Elena and Perneczky, Robert and Diehl-Schmid, Janine and Alexopoulos, Panagiotis and Kurz, Alexander and Rainero, Innocenzo and Rubino, Elisa and Pinessi, Lorenzo and Rogaeva, Ekaterina and St George-Hyslop, Peter and Rossi, Giacomina and Tagliavini, Fabrizio and Giaccone, Giorgio and Rowe, James B and Schlachetzki, Johannes C.M and Uphill, James and ... and Int FTD-Genomics Consortium and International FTD-Genomics Consortium
PLoS Medicine, ISSN 1549-1277, 01/2018, Volume 15, Issue 1, p. e1002487
Background Converging evidence suggests that immune-mediated dysfunction plays an important role in the pathogenesis of frontotemporal dementia (FTD). Although... 
COMMON VARIANTS | MEDICINE, GENERAL & INTERNAL | LOBAR DEGENERATION | TAU | LOCI | AMYOTROPHIC-LATERAL-SCLEROSIS | RISK VARIANTS | IDENTIFIES 7 | PROGRESSIVE SUPRANUCLEAR PALSY | CORTICOBASAL DEGENERATION | PARKINSONS-DISEASE | Frontotemporal Dementia - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Humans | Middle Aged | Aged | Polymorphism, Single Nucleotide | Medical research | Psoriasis | Genes | Genomics | HLA histocompatibility antigens | Amyotrophic lateral sclerosis | Genomes | Crohn's disease | Disease susceptibility | Research | Rheumatoid factor | Histocompatibility antigens | Analysis | Medicine, Experimental | Genetic aspects | Single nucleotide polymorphisms | Ulcerative colitis | Protein binding | Care and treatment | Immune response | Development and progression | Genotype | Frontotemporal dementia | Health aspects | Brain | Disease | Pathogenesis | Central nervous system | Disorders | Consortia | Signal transduction | Autopsy | Neurodegeneration | LRRK2 protein | University colleges | Internal medicine | Gene expression | Patients | Diseases | Microglia | Celiac disease | Neurology | Pathology | Pleiotropy | Hospitals | Rheumatoid arthritis | Clinical medicine | Mutation | Dementia | Enrichment | Neurosciences | Mental disorders | Laboratories | Linkage disequilibrium | Mental health | Clinical trials | Diabetes mellitus (insulin dependent) | Arthritis | Leucine | Macrophages | Genetic analysis | Dementia disorders | Degeneration | Paralysis | Supervision | Transposons | Diabetes mellitus | Loci | Medicine | White blood cells | Brain research | Histocompatibility antigen HLA | Autoimmune diseases | Psychiatry
Journal Article
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 7/2011, Volume 122, Issue 1, pp. 99 - 110
Journal Article