|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
CausalMutation
|
CLINVAR |
Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles.
|
26308724 |
2015 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association.
|
25355838 |
2014 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
CausalMutation
|
CLINVAR |
Spectrum of NOTCH3 mutations in Korean patients with clinically suspicious cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
|
24139282 |
2014 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
CausalMutation
|
CLINVAR |
Headache among CADASIL patients with R544C mutation: prevalence, characteristics, and associations.
|
23847153 |
2014 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
CausalMutation
|
CLINVAR |
A homozygous NOTCH3 mutation p.R544C and a heterozygous TREX1 variant p.C99MfsX3 in a family with hereditary small vessel disease of the brain.
|
23602593 |
2013 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
CausalMutation
|
CLINVAR |
Diversity of stroke presentation in CADASIL: study from patients harboring the predominant NOTCH3 mutation R544C.
|
21852154 |
2013 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Hypomorphic NOTCH3 alleles do not cause CADASIL in humans.
|
24000151 |
2013 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.
|
20298421 |
2010 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
CausalMutation
|
CLINVAR |
The remarkably variable expressivity of CADASIL: report of a minimally symptomatic man at an advanced age.
|
19252787 |
2009 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
CausalMutation
|
CLINVAR |
Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese.
|
19242647 |
2009 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
|
15818833 |
2005 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies.
|
16009764 |
2005 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Gene symbol: NOTCH3. Disease: CADASIL.
|
15300988 |
2004 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Detection of the founder effect in Finnish CADASIL families.
|
15378071 |
2004 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
CADASIL-associated Notch3 mutations have differential effects both on ligand binding and ligand-induced Notch3 receptor signaling through RBP-Jk.
|
15350543 |
2004 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients.
|
15364702 |
2004 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
|
12589106 |
2003 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.
|
12810003 |
2003 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke.
|
12136071 |
2002 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Reversible coma with raised intracranial pressure: an unusual clinical manifestation of CADASIL.
|
11810186 |
2002 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia.
|
12146805 |
2002 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings.
|
11559313 |
2001 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Splice site mutation causing a seven amino acid Notch3 in-frame deletion in CADASIL.
|
10802807 |
2000 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains.
|
10854111 |
2000 |
|
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT, WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY, TYPE 1
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Identification of a novel mutation C144F in the Notch3 gene in an Australian CADASIL pedigree.
|
11058919 |
2000 |