Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles

Clinical Significance of Cerebral Microbleeds Locations in CADASIL with R544C NOTCH3 Mutation

(2015) Jung Seok Lee et al.   PLoS One

Changing clinical patterns and increasing prevalence in CADASIL

(2014) F. C. Moreton et al.   ACTA NEUROLOGICA SCANDINAVICA

CADASIL in central Italy: a retrospective clinical and genetic study in 229 patients

(2014) Silvia Bianchi et al.   JOURNAL OF NEUROLOGY

Characteristics of CADASIL in Chinese mainland patients

(2014) Jia-Tang Zhang et al.   NEUROLOGY INDIA

Headache among CADASIL patients with R544C mutation: Prevalence, characteristics, and associations

(2013) Jay Chol Choi et al.   CEPHALALGIA

Spontaneous intracerebral hemorrhage in CADASIL

(2013) Lifei Lian et al.   JOURNAL OF HEADACHE AND PAIN

A homozygous NOTCH3 mutation p.R544C and a heterozygous TREX1 variant p.C99MfsX3 in a family with hereditary small vessel disease of the brain

(2013) Bing-Wen Soong et al.   Journal of the Chinese Medical Association

Spectrum of NOTCH3 mutations in Korean patients with clinically suspicious cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

(2013) Young-Eun Kim et al.   NEUROBIOLOGY OF AGING

Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

(2012) S. Testi et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

Diversity of Stroke Presentation in CADASIL: Study from Patients Harboring the Predominant NOTCH3 Mutation R544C

(2011) Jay Chol Choi et al.   Journal of Stroke & Cerebrovascular Diseases

NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL

(2010) Z. Wang et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Clinical Spectrum of CADASIL and the Effect of Cardiovascular Risk Factors on Phenotype

(2010) Poneh Adib-Samii et al.   STROKE

Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain

(2009) Marie Monet-Leprêtre et al.   BRAIN

Homozygosity for a NOTCH3 mutation in a 65-year-old CADASIL patient with mild symptoms

(2009) M. K. Liem et al.   JOURNAL OF NEUROLOGY

Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese

(2009) Y.-C. Lee et al.   JOURNAL OF NEUROLOGY

CADASIL

(2009) Hugues Chabriat et al.   LANCET NEUROLOGY