1Sourander P, Walinder J. Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease[J]. Acta Neuropathol (Berl), 1977,39(3):247-254.
2Bousser MG,Tournier-Lasserve E. Summary of the proceedings of the First International Workshop on CADASIL[J].Stroke,1994,25(3):704-707.
7Tournier-Lasserve E, Joutel A, Melki J, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12[J]. Nat Genet,1993,3(3):256-259.
8Joutel A, Corpechot C, Ducros A, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia[J].Nature,1996,383(6602):707-710.
9Dichgans M. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: phenotypic and mutational spectrum[J].J Neurol Sci,2002,203-204(1):77-80.
10Joutel A, Vahedi K,Corpechot C,et al. Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients[J].Lancet,1997,350(9090):1511-1515.
二级参考文献38
1[3]Sourander P, Walinder J. Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease. Acta Neuropathol(Berl), 1977, 39:247-254.
2[4]Bousser MG, Tournier-Lasserve E. Summary of the proceedings of the First International Workshop on CADASIL. Paris, May 19-21,1993. Stroke, 1994, 25:704-707.
3[5]Desmond DW, Moroney JT, Lynch T, et al. The natural history of CADASIL: a pooled analysis of previously published cases. Stroke,1999, 30:1230-1233.
4[6]Lesnik Oberstein SA, Jukema JW, Van Duinen SG, et al. Myocardial infarction in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Medicine (Baltimore), 2003, 82:251-256.
5[7]Chabriat H, Levy C, Taillia H, et al. Patterns of MRI lesions in CADASIL. Neurology, 1998, 51:452-457.
6[8]Chabriat H, Mrissa R, Levy C, et al. Brain stem MRI single abnormalities in CADASIL. Stroke, 1999, 30:457-459.
7[9]Kanitakis J, Thobois S, Claudy A, et al. CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): a neurovascular disease diagnosed by ultrastructural examination of the skin. J Cutan Pathol, 2002, 29:498-501.
8[10]Markus HS, Martin RJ, Simpson MA, et al. Diagnostic strategies in CADASIL. Neurology, 2002, 59:1134-1138.
9[11]Joutel A, Corpechot C, Ducros A, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature, 1996, 383:707-710.
10[12]Rumbaugh JA, LaDuca JR, Shun Y, et al. CADASIL: the dermatologic diagnosis of a neurologic disease. Cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy. J Am Acad Dermatol, 2000, 43:1128-1130.