1Sourander P,Wailinder J. Hereditary multi-infarct dementia. Morphological and clinical studies of a new diseasse [J]. Acta Neuropathol Berl, 1977,39 ( 3 ) : 247-254.
3Tournier-Lasserve E,Joutel A,Melki J,et al. Cerebral autosomal dominant arteriopathy with subcortical infacts and leukoencephalopathy maps to chromosome 19q12[J]. Nat Genet, 1993,3 ( 3 ) :256-259.
4Joutel A, Vahedi K, Corpechot C, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia [J]. Nature, 1996,383:707-710.
6Finnila S,Tuisku S, Herva R, et al. A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL[ J]. J Mol Med,2001,79 ( 11 ) :641-647.
7Malandrini A, Carrera P, Ciacci G, et al. Unusual clinical features and early brain MRI lesions in a family with cererbal autosomal dominant arteriopathy [ J ]. Neurology, 1997,48 ( 5 ) : 1200-1203.
8Mellies JK, Baumer T, Muller JA, et al. SPECT study of a German CADASIL family:a phenotype with migraine and progressive dementia only[J]. Neurology, 1998,50(6) : 1715-1721.
9Chabriat H, Mrissa R, Levy C,et al. Brain stemMRI signal abnormalities in CADASIL [ J ]. Stroke, 1999,30 ( 2 ) :457-459.
10Chabriat H,Pappata S,Poupon C, ct al. Clinical severity in CADASIL related to uhrastructural damage in white matter [ J]. Stroke, 1999,30(3 ) :2637-2643.
1Roy B, Maksemous N, Smith RA , et al. Two novel mutations and apreviously unreported intronic polymorphism in the NOTCH3 gene[J]. Mutat Res,2012,732(1 -2) :3 -8.
