[1] Machowska-Sempruch K, Bajer-Czajkowska A, Makarewicz K, et al. A novel NOTCH3 gene mutation in a polish CADASIL family [J]. J Stroke Cerebrovasc Dis, 2019, 28(3): 574-576
[2] 吕 燕, 吴时燕, 张 杉, 等. 常染色体显性遗传脑动脉病(附1例报告及文献复习) [ J ]. 中国临床神经科学, 2019, 27(6): 633-643.
[3] Yin X, Wu D, Wan J, et al. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: phenotypic and mutational spectrum in patients from mainland China [J]. Int J Neurosci, 2015, 125(8): 585-592.
[4] Ho C S, Mondry A.CADASIL presenting as schizophreniform organic psychosis[J].Gen Hosp Psychiatry, 2015, 37 (3): e11273, e13.
[5] Oh J H, Kang B S, Choi J C. CADASIL initially presented with a seizure[J]. J Epilepsy Res, 2016, 6(2): 104-106.
[6] 袁 云. CADASIL的诊断与鉴别诊断[J]. 中国神经精神疾病杂志, 2007, 33(11):641-643.
[7] Ban S, Wang H, Wang M, et al.Diffuse tract damage in CADASIL is correlated with global cognitive impairment [J]. Eur Neurol, 2019, 4: 1-8.
[8] 孙启英, 李雯雯, 周亚芳, 等. 两个伴皮层下梗死和白质脑病的常染色体显性遗传性脑动脉病家系NOTCH3基因的突变分析[J]. 中华医学遗传学杂志, 2017(6): 816-820.
[9] 牛 媛, 王建林. 常染色体显性遗传病伴皮质下梗死和白质脑病的临床研究进展[J]. 国际遗传学杂志, 2017(3):177-182.
[10] 任志霞, 时英英, 陈祖芝, 等. 来自19个家系37例伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病的临床影像及NOTCH3基因突变特征分析[J]. 中华神经科杂志, 2017(8): 613-618.
[11] Wen Z, Zhou L, Liu B W, et al.Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: NOTCH3 gene mutation and clinical features[J].Acad J Chin PLA Med Sch, 2017, 38 (3):221-225.
[12] Schoemaker D, Quiroz Y T, Torrico-Teave H, et al. Clinical and research applications of magnetic resonance imaging in the study of CADASIL[J]. Neurosci Lett, 2019, 698: 173-179.
[13] Stojanov D, Aracki-Trenkic A, Vojinovic S, et al.Imaging characteristics of cerebral autosomal dominant arteriopathy with subcortical infacts and leukoencephalopathy( CADASIL)[J].Bosn J Basic Med Sci, 2015, 15(1): 1-8.
[14] Stojanov D, Aracki-Trenkic A, Vojinovic S, et al. Imaging characteristics of cerebral autosomal dominant arteriopathy with subcortical infacts and leukoencephalopathy( CADASIL)[J].Bosn J Basic Med Sci, 2015, 15(1): 1-8.