X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1046) 1046
Book Review (157) 157
Publication (81) 81
Book Chapter (15) 15
Conference Proceeding (8) 8
Magazine Article (4) 4
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (826) 826
humans (821) 821
cadasil (801) 801
male (514) 514
clinical neurology (497) 497
female (486) 486
middle aged (482) 482
adult (368) 368
neurosciences (361) 361
stroke (345) 345
magnetic resonance imaging (327) 327
autosomal-dominant arteriopathy (319) 319
subcortical infarcts (312) 312
cadasil - genetics (297) 297
aged (285) 285
leukoencephalopathy (280) 280
dementia (268) 268
receptor, notch3 (266) 266
mutation (239) 239
receptors, notch - genetics (220) 220
cadasil - pathology (212) 212
brain - pathology (196) 196
neurology (188) 188
notch3 (182) 182
cadasil - diagnosis (180) 180
cadasil - complications (157) 157
notch3 mutations (136) 136
spectrum (136) 136
peripheral vascular disease (130) 130
migraine (126) 126
risk factors (122) 122
mri (119) 119
genetic aspects (116) 116
cadasil - physiopathology (114) 114
vascular dementia (107) 107
diagnosis (104) 104
leukoencephalopathy cadasil (103) 103
disease (102) 102
pedigree (101) 101
brain (99) 99
phenotype (98) 98
pathology (91) 91
psychiatry (91) 91
mutations (88) 88
animals (85) 85
diagnosis, differential (79) 79
dna mutational analysis (75) 75
medicine & public health (75) 75
small vessel disease (74) 74
abridged index medicus (71) 71
research (71) 71
aged, 80 and over (70) 70
alzheimers-disease (70) 70
proto-oncogene proteins - genetics (66) 66
neuropsychological tests (65) 65
dementia, multi-infarct - genetics (64) 64
mutation - genetics (64) 64
biopsy (63) 63
neuroimaging (63) 63
receptors, notch (62) 62
genetics (61) 61
lesions (60) 60
medicine (59) 59
magnetic resonance imaging - methods (56) 56
notch3 gene (56) 56
disease progression (55) 55
brain - blood supply (53) 53
stroke - genetics (52) 52
abnormalities (51) 51
gene mutations (51) 51
analysis (50) 50
cadasil - metabolism (50) 50
white-matter (49) 49
cadasil - diagnostic imaging (48) 48
neuroradiology (48) 48
small-vessel disease (48) 48
cognitive impairment (47) 47
genetic predisposition to disease (47) 47
cognitive ability (46) 46
gene (45) 45
cadasil patients (44) 44
family (44) 44
medicine, general & internal (44) 44
prevalence (44) 44
receptors, cell surface (44) 44
families (43) 43
skin - pathology (43) 43
cadasil - epidemiology (42) 42
case-control studies (42) 42
hypertension (42) 42
mutation, missense (42) 42
health aspects (41) 41
risk-factors (41) 41
young adult (41) 41
genes (40) 40
muscle (40) 40
patients (40) 40
exons (39) 39
mice (39) 39
cadasil - psychology (38) 38
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (979) 979
Japanese (23) 23
Spanish (19) 19
French (18) 18
German (13) 13
Chinese (6) 6
Russian (3) 3
Polish (1) 1
Serbian (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of the Neurological Sciences, ISSN 0022-510X, 2015, Volume 359, Issue 1, pp. 347 - 350
Journal Article
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 07/2018, Volume 390, pp. 121 - 128
CADASIL is an inherited cerebrovascular disease caused by mutations in the gene. Notch signaling is involved in a broad spectrum of function, from the cell... 
Fibroblasts | CADASIL | Notch3 protein | NOTCH3 gene | SUBCORTICAL INFARCTS | ACTIVATION | COLLAGEN | VARIANTS | BIOPSY | NEUROSCIENCES | CLINICAL NEUROLOGY | FAMILY | AUTOSOMAL-DOMINANT ARTERIOPATHY | JAGGED1 | MUTATIONS | LEUKOENCEPHALOPATHY CADASIL | Analysis | Skin | Index Medicus
Journal Article
RADIOLOGY, ISSN 0033-8419, 07/2013, Volume 268, Issue 1, pp. 170 - 180
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2015, Volume 354, Issue 1, pp. 63 - 69
Journal Article