X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (376) 376
humans (370) 370
cadasil (364) 364
clinical neurology (202) 202
male (190) 190
female (178) 178
middle aged (176) 176
stroke (165) 165
neurosciences (155) 155
adult (134) 134
autosomal-dominant arteriopathy (132) 132
magnetic resonance imaging (132) 132
subcortical infarcts (130) 130
dementia (124) 124
cadasil - genetics (118) 118
leukoencephalopathy (116) 116
mutation (111) 111
receptor, notch3 (105) 105
brain - pathology (91) 91
aged (89) 89
neurology (81) 81
receptors, notch - genetics (81) 81
cadasil - pathology (74) 74
notch3 (71) 71
cadasil - diagnosis (68) 68
cadasil - complications (66) 66
migraine (65) 65
notch3 mutations (64) 64
animals (62) 62
genetic aspects (60) 60
vascular dementia (57) 57
leukoencephalopathy cadasil (52) 52
diagnosis (51) 51
spectrum (51) 51
pedigree (50) 50
risk factors (50) 50
diagnosis, differential (47) 47
medicine & public health (47) 47
mutations (47) 47
phenotype (47) 47
disease (46) 46
pathology (44) 44
psychiatry (44) 44
cadasil - physiopathology (42) 42
research (42) 42
genetics (41) 41
mri (41) 41
peripheral vascular disease (38) 38
brain (37) 37
dementia, multi-infarct - genetics (35) 35
mutation - genetics (35) 35
proto-oncogene proteins - genetics (35) 35
dna mutational analysis (34) 34
receptors, notch (34) 34
alzheimers-disease (32) 32
gene (31) 31
brain - blood supply (30) 30
medicine (29) 29
small vessel disease (29) 29
stroke - genetics (29) 29
biopsy (28) 28
small-vessel disease (28) 28
gene mutations (27) 27
neuroradiology (27) 27
cognitive ability (25) 25
dementia, multi-infarct - pathology (25) 25
age of onset (24) 24
cadasil patients (24) 24
genetic predisposition to disease (24) 24
receptors, cell surface (24) 24
cadasil - metabolism (23) 23
mice (23) 23
neuroimaging (23) 23
abridged index medicus (22) 22
exons (22) 22
headache (22) 22
multidisciplinary sciences (22) 22
neuropsychological tests (22) 22
risk-factors (22) 22
abnormalities (21) 21
analysis (21) 21
biochemistry & molecular biology (21) 21
genes (21) 21
health aspects (21) 21
internal medicine (21) 21
prevalence (21) 21
smooth muscle (21) 21
white-matter (21) 21
cognitive impairment (20) 20
ischemic-stroke (20) 20
leukoaraiosis (20) 20
medicine, general & internal (20) 20
carasil (19) 19
cerebral arteries - pathology (19) 19
familial hemiplegic migraine (19) 19
family (19) 19
genetics & heredity (19) 19
magnetic resonance imaging - methods (19) 19
notch3 gene (19) 19
patients (19) 19
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (445) 445
French (10) 10
Spanish (10) 10
German (6) 6
Japanese (6) 6
Polish (2) 2
Russian (2) 2
Danish (1) 1
Hungarian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Stroke, ISSN 0039-2499, 07/2016, Volume 47, Issue 7, pp. 1702 - 1709
Journal Article
Journal of insurance medicine (New York, N.Y.), ISSN 0743-6661, 2014, Volume 44, Issue 2, pp. 127 - 129
A rare hereditary disorder characterized by migraine headaches, transient ischemic attacks, strokes, cognitive decline, and dementia. 
Magnetic Resonance Imaging | CADASIL - pathology | Brain - physiopathology | Humans | Brain - pathology | CADASIL - physiopathology | Syndrome
Journal Article
Journal Article
Journal Article
Journal Article
Expert Opinion on Orphan Drugs, ISSN 2167-8707, 09/2013, Volume 1, Issue 9, pp. 695 - 703
Journal Article
Journal Article
Neuro-ophthalmology, ISSN 0165-8107, 8/2012, Volume 36, Issue 4, pp. 158 - 164
Prodromic or acute visual symptoms are characteristic of many reversible white matter syndromes, which may motivate consultation with an ophthalmologist or... 
Loss of consciousness | Encephalitis | Scotoma | PRES | TOXIC LEUKOENCEPHALOPATHY | MRI | MIGRAINE | LESIONS | FEATURES | CADASIL | NEUROMYELITIS-OPTICA | OPHTHALMOLOGY | INFARCTS
Journal Article
Current Molecular Medicine, ISSN 1566-5240, 06/2007, Volume 7, Issue 4, pp. 427 - 445
The Notch signaling pathway is involved in a wide variety of highly conserved developmental processes in mammals. Importantly, mutations of the Notch protein... 
Delta-like protein | Notch gene | O-Fucose modification | Coagulation factor | Endoplasmic reticulum | Epidermal Growth Factor | MEDICINE, RESEARCH & EXPERIMENTAL | DROSOPHILA WING DEVELOPMENT | FACTOR-LIKE MODULES | ALAGILLE-SYNDROME | ACUTE LYMPHOBLASTIC-LEUKEMIA | UDP-D-XYLOSE | AUTOSOMAL-DOMINANT ARTERIOPATHY | O-LINKED FUCOSE | NULL FEMALE MICE | CELL LINE HEPG2 | FACTOR-LIKE REPEATS | Alagille Syndrome - enzymology | CADASIL - pathology | Receptors, Notch - metabolism | Fucose - metabolism | Humans | N-Acetylglucosaminyltransferases - genetics | Receptors, Notch - genetics | Alagille Syndrome - pathology | Endoplasmic Reticulum - pathology | Intercellular Signaling Peptides and Proteins - metabolism | Alagille Syndrome - genetics | Serrate-Jagged Proteins | CADASIL - therapy | Membrane Proteins - metabolism | Jagged-1 Protein | Calcium-Binding Proteins - metabolism | Endoplasmic Reticulum - enzymology | CADASIL - enzymology | Fucosyltransferases - genetics | Multiple Sclerosis - enzymology | Membrane Proteins - genetics | Intercellular Signaling Peptides and Proteins - genetics | Intracellular Signaling Peptides and Proteins | Fucose - genetics | Multiple Sclerosis - genetics | Glycosylation | Protein Structure, Tertiary - genetics | Signal Transduction - genetics | Alagille Syndrome - therapy | Multiple Sclerosis - therapy | CADASIL - genetics | N-Acetylglucosaminyltransferases - metabolism | Protein Modification, Translational | Fucosyltransferases - metabolism | Leukemia, T-Cell - enzymology | Leukemia, T-Cell - genetics | Multiple Sclerosis - pathology | Leukemia, T-Cell - pathology | Leukemia, T-Cell - therapy | Calcium-Binding Proteins - genetics
Journal Article