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

Changing clinical patterns and increasing prevalence in CADASIL

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

The first deep intronic mutation in the NOTCH3 gene in a family with late-onset CADASIL

(2013) Silvia Bianchi 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

The minimum prevalence of CADASIL in northeast England

(2012) S. K. Narayan et al.   NEUROLOGY

The Cerebral Autosomal-Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale

(2012) Francesca Pescini et al.   STROKE

First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family

(2011) Raffaella Valenti et al.   JOURNAL OF NEUROLOGY

High frequency of exon 10 mutations in the NOTCH3 gene in Italian CADASIL families: phenotypic peculiarities

(2010) S. Bianchi et al.   JOURNAL OF NEUROLOGY

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

CADASIL

(2009) Hugues Chabriat et al.   LANCET NEUROLOGY

High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

(2009) Alessia Cappelli et al.   NEUROSCIENCE LETTERS

Different Clinical Phenotypes in Monozygotic CADASIL Twins With a Novel NOTCH3 Mutation

(2009) Kati Mykkänen et al.   STROKE

A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient

(2007) Francesca Pescini et al.   JOURNAL OF THE NEUROLOGICAL SCIENCES