X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (639) 639
Newspaper Article (240) 240
Publication (175) 175
Book Chapter (15) 15
Book Review (2) 2
Conference Proceeding (2) 2
Data Set (1) 1
Magazine Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (294) 294
clinical neurology (243) 243
female (229) 229
male (229) 229
index medicus (227) 227
aged (208) 208
middle aged (200) 200
article (157) 157
neurosciences (153) 153
dementia (141) 141
neurology (138) 138
magnetic resonance imaging (103) 103
aged, 80 and over (99) 99
pathology (97) 97
progressive supranuclear palsy (90) 90
frontotemporal dementia (86) 86
alzheimers-disease (80) 80
brain - pathology (77) 77
alzheimer's disease (69) 69
frontotemporal lobar degeneration (69) 69
atrophy (68) 68
aphasia (67) 67
diagnosis (66) 66
adult (63) 63
corticobasal degeneration (62) 62
tau (56) 56
brain (52) 52
mri (51) 51
abridged index medicus (50) 50
mental disorders (49) 49
voxel-based morphometry (49) 49
neuropsychological tests (48) 48
tdp-43 (47) 47
disease (46) 46
retrospective studies (44) 44
primary progressive aphasia (41) 41
nervous system diseases (39) 39
degeneration (38) 38
neuroimaging (37) 37
age of onset (36) 36
apraxia (36) 36
diagnosis, differential (36) 36
medicine & public health (36) 36
disease progression (34) 34
dementia - pathology (33) 33
neurodegenerative diseases (33) 33
alzheimer disease - pathology (32) 32
amyotrophic-lateral-sclerosis (32) 32
mutation (32) 32
brain - metabolism (31) 31
neuropathology (30) 30
positron-emission tomography (30) 30
supranuclear palsy, progressive - pathology (30) 30
parkinsons-disease (29) 29
cohort studies (27) 27
criteria (27) 27
dna-binding proteins - metabolism (27) 27
research (27) 27
atrophy - pathology (26) 26
cerebral cortex - pathology (26) 26
diagnostic-criteria (26) 26
magnetic resonance imaging - methods (26) 26
analysis (25) 25
motor-neuron disease (25) 25
mutations (25) 25
nervous system (25) 25
autopsy (24) 24
nonfluent aphasia (24) 24
positron emission tomography (24) 24
semantic dementia (24) 24
alzheimers disease (23) 23
amyotrophic lateral sclerosis (23) 23
apraxia of speech (23) 23
lobar degeneration (23) 23
speech (23) 23
tau proteins - metabolism (23) 23
age (22) 22
frontotemporal dementia - genetics (22) 22
patients (22) 22
risk factors (22) 22
tau proteins - genetics (22) 22
alzheimer’s disease (21) 21
brain - physiopathology (21) 21
geriatrics & gerontology (20) 20
language (20) 20
neurodegeneration (20) 20
neurodegenerative diseases - pathology (20) 20
phenotype (20) 20
psychiatry (20) 20
case-control studies (19) 19
cortex (19) 19
lewy bodies (19) 19
medical research (19) 19
nutritional and metabolic diseases (19) 19
parkinsonism (19) 19
supranuclear palsy (19) 19
tau protein (19) 19
3 variants (18) 18
frontotemporal dementia - pathology (18) 18
genotype (18) 18
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Lancet Neurology, ISSN 1474-4422, 09/2018, Volume 17, Issue 9, pp. 735 - 737
TDP-43 was first reported to be a key biological component of frontotemporal lobar degeneration and amyotrophic lateral sclerosis in 2006.1 Subsequently,... 
Haplotypes | Humans | Apolipoproteins E | TDP-43 Proteinopathies | Alzheimer Disease | Hippocampus | Sclerosis | Cohort Studies | DNA-Binding Proteins | Studies | Proteins | Pathology | Neurodegeneration | Apolipoprotein E | Accounting | Older people | Religious orders | Memory | Alzheimers disease
Journal Article
Brain, ISSN 0006-8950, 02/2018, Volume 141, Issue 2, pp. 324 - 331
This scientific commentary refers to 'Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies' by Forrest et al.... 
TAU | DEMENTIA | CHROMOSOME-17 | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | CLINICAL NEUROLOGY
Journal Article
The Lancet Neurology, ISSN 1474-4422, 03/2015, Volume 14, Issue 3, pp. 236 - 237
  In some instances, family members can be afflicted with motor neuron disease, which can be even more devastating than frontotemporal dementia.3 The first... 
TAU | LOBAR DEGENERATION | GENETICS | C9ORF72 | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Neuropsychological Tests | Humans | Brain - pathology | Female | Male | Cognition Disorders - genetics | Asymptomatic Diseases | Mutation - genetics | Invisibility | Dementia | Studies | Biomarkers | Medical imaging | Mutation | Alzheimers disease
Journal Article
Neuropathology and applied neurobiology, ISSN 0305-1846, 6/2016, Volume 42, Issue 4, pp. 390 - 393
Journal Article
Seminars in Neurology, ISSN 0271-8235, 04/2019, Volume 39, Issue 2, pp. 264 - 273
Abstract Tauopathies are rare neurodegenerative disorders related to microtubule-associated protein tau, which functions to stabilize microtubules.... 
Review Article | tau | FTLD-tau | MAPT | tau-PET | ARGYROPHILIC GRAIN DISEASE | ALZHEIMERS-DISEASE | FRONTOTEMPORAL DEMENTIA | PICKS-DISEASE | NEUROPATHOLOGIC CRITERIA | CEREBROSPINAL-FLUID | CLINICAL NEUROLOGY | POSITRON-EMISSION-TOMOGRAPHY | PROGRESSIVE SUPRANUCLEAR PALSY | CORTICOBASAL DEGENERATION | TAU-PATHOLOGY
Journal Article
Neuron, ISSN 0896-6273, 10/2011, Volume 72, Issue 2, pp. 245 - 256
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 4/2016, Volume 131, Issue 4, pp. 571 - 585
In this study, we update the TDP-43 in Alzheimer’s disease staging scheme by assessing the topography of TDP-43 in 193 cases of Alzheimer’s disease, in 14... 
Pathology | Neurosciences | Medicine & Public Health | Alzheimer’s disease | Staging | TDP-43 | Limbic | Brainstem | Insular cortex | brainstem | limbic | insular cortex | staging
Journal Article
Neurology, ISSN 0028-3878, 08/2015, Volume 85, Issue 5, pp. 404 - 412
Journal Article
Journal of Molecular Neuroscience, ISSN 0895-8696, 11/2011, Volume 45, Issue 3, pp. 384 - 389
A clinically and pathologically heterogeneous type of frontotemporal lobar degeneration has abnormal tau pathology in neurons and glia (FTLD-tau). Familial... 
Neurochemistry | Neurology | Neurosciences | Biomedicine | Progressive supranuclear palsy | Proteomics | Corticobasal degeneration | Pick’s disease | Cell Biology | Corticobasal syndrome | Frontotemporal lobar degeneration-tau | Richardson syndrome | Pick's disease | GENE-MUTATIONS | PROTEIN-TAU | CYTOSKELETAL PATHOLOGY | ALZHEIMER-DISEASE | DEMENTIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | 4R TAUOPATHY | PICKS-DISEASE | NEUROSCIENCES | BASAL GANGLIONIC DEGENERATION | Pick Disease of the Brain - physiopathology | Frontotemporal Lobar Degeneration - pathology | Supranuclear Palsy, Progressive - pathology | Supranuclear Palsy, Progressive - physiopathology | Tauopathies - genetics | Humans | Tauopathies - pathology | tau Proteins - metabolism | Frontotemporal Lobar Degeneration - physiopathology | Pick Disease of the Brain - genetics | Pick Disease of the Brain - pathology | Tauopathies - metabolism | tau Proteins - genetics | Frontotemporal Lobar Degeneration - genetics | Supranuclear Palsy, Progressive - genetics | Nervous system | Development and progression | Degeneration | Research | Pathology, Molecular | Niemann-Pick disease | Alternative splicing | Brain | Brain architecture | Neurodegenerative diseases | Astrocytes | Neurons | Neuropathology | biomarkers | Amino acids | Anatomy | Tau protein | Microtubules | Mutation | Differentiation | Frontotemporal dementia | Plaques | progressive supranuclear palsy | frontotemporal lobar degeneration – tau | corticobasal degeneration | corticobasal syndrome
Journal Article