Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Phenotypic and mutational spectrum in patients from mainland China

Interpretation ofNOTCH3mutations in the diagnosis of CADASIL

(2014) Julie W Rutten et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Screening for NOTCH3 Gene Mutations Among 151 Consecutive Korean Patients with Acute Ischemic Stroke

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

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 gene mutations in subjects clinically suspected of CADASIL

(2011) Lorena Mosca et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

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

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

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

(2009) Saara Tikka et al.   BRAIN

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

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

Report of two Chinese families and a review of Mainland Chinese CADASIL patients

(2009) Xin-zhen Yin et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES

CADASIL

(2009) Hugues Chabriat et al.   LANCET NEUROLOGY

Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients

(2009) L. Pantoni et al.   NEUROLOGY

On the Etiology of Incident Brain Lacunes

(2008) Alida A. Gouw et al.   STROKE