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4. Archetypal Arg169Cys mutation in NOTCH3 does not drive the pathogenesis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy via a loss-of-function mechanism. Cognat E; Baron-Menguy C; Domenga-Denier V; Cleophax S; Fouillade C; Monet-Leprêtre M; Dewerchin M; Joutel A Stroke; 2014 Mar; 45(3):842-9. PubMed ID: 24425116 [TBL] [Abstract][Full Text] [Related]
5. New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Abramycheva N; Stepanova M; Kalashnikova L; Zakharova M; Maximova M; Tanashyan M; Lagoda O; Fedotova E; Klyushnikov S; Konovalov R; Sakharova A; Illarioshkin S J Neurol Sci; 2015 Feb; 349(1-2):196-201. PubMed ID: 25623805 [TBL] [Abstract][Full Text] [Related]
6. A novel Notch3 deletion mutation in a Chinese patient with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Weiming F; Yuliang W; Youjie L; Xinsheng L; Shuyang X; Zhaoxia L J Clin Neurosci; 2013 Feb; 20(2):322-3. PubMed ID: 23151434 [TBL] [Abstract][Full Text] [Related]
7. A new de novo Notch3 mutation causing CADASIL. Coto E; Menéndez M; Navarro R; García-Castro M; Alvarez V Eur J Neurol; 2006 Jun; 13(6):628-31. PubMed ID: 16796587 [TBL] [Abstract][Full Text] [Related]
8. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese. Lee YC; Yang AH; Liu HC; Wong WJ; Lu YC; Chang MH; Soong BW J Neurol Sci; 2006 Jul; 246(1-2):111-5. PubMed ID: 16580020 [TBL] [Abstract][Full Text] [Related]
9. Two novel mutations of the NOTCH3 gene in Korean patients with CADASIL. Kim Y; Kim JS; Kim G; No YJ; Yoo HW Mutat Res; 2006 Jan; 593(1-2):116-20. PubMed ID: 16256149 [TBL] [Abstract][Full Text] [Related]
10. [CADASIL and CARASIL]. López JI; Vilanova JR Neurologia; 2009 Mar; 24(2):125-30. PubMed ID: 19322691 [TBL] [Abstract][Full Text] [Related]
11. [Study of the familiar form of vascular dementia (CADASIL)]. Takahashi K; Yoshizaki K Nihon Shinkei Seishin Yakurigaku Zasshi; 2007 Jun; 27(3):141-5. PubMed ID: 17633526 [TBL] [Abstract][Full Text] [Related]
12. De novo mutation in the NOTCH3 gene causing CADASIL. Stojanov D; Grozdanović D; Petrović S; Benedeto-Stojanov D; Stefanović I; Stojanović N; Ilić DN Bosn J Basic Med Sci; 2014 Feb; 14(1):48-50. PubMed ID: 24579972 [TBL] [Abstract][Full Text] [Related]
13. [Identification of a novel NOTCH3 mutation in a family featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy]. Zhu Y; Wang J; Wu Y; Wang G; Hu B; Xu A Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):578-81. PubMed ID: 25297585 [TBL] [Abstract][Full Text] [Related]
14. Two novel mutations in NOTCH3 gene causes cerebral autosomal dominant arteriopathy with subcritical infarct and leucoencephalopathy in two Chinese families. Zhu Y; Wang J; Wu Y; Wang G; Hu B Int J Clin Exp Pathol; 2015; 8(2):1321-7. PubMed ID: 25973016 [TBL] [Abstract][Full Text] [Related]
15. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a patient from Sri Lanka. De Silva KR; Gamage R; Dunuwille J; Gunarathna D; Sirisena D; Weerasinghe A; Amarasinghe PH; Hosomi A; Mizuno T J Clin Neurosci; 2009 Nov; 16(11):1492-3. PubMed ID: 19683925 [TBL] [Abstract][Full Text] [Related]
16. The prenatal diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by mutation analysis. Milunsky A; Konialis C; Shim SH; Maher TA; Spengos K; Ito M; Pangalos C Prenat Diagn; 2005 Nov; 25(11):1057-8. PubMed ID: 16302168 [TBL] [Abstract][Full Text] [Related]
17. A case report about CADASlL: mutation in the NOTCH 3 receptor. Delibas S; Guven H; Comoglu SS Acta Neurol Taiwan; 2009 Dec; 18(4):262-6. PubMed ID: 20329594 [TBL] [Abstract][Full Text] [Related]
18. [CADASIL syndrome - cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]. Dziewulska D; Kwieciński H Neurol Neurochir Pol; 2008; 42(2):123-30. PubMed ID: 18512169 [TBL] [Abstract][Full Text] [Related]
19. High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Cappelli A; Ragno M; Cacchiò G; Scarcella M; Staffolani P; Pianese L Neurosci Lett; 2009 Sep; 462(2):176-8. PubMed ID: 19576955 [TBL] [Abstract][Full Text] [Related]
20. Notch3 Arg170Cys knock-in mice display pathologic and clinical features of the neurovascular disorder cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Wallays G; Nuyens D; Silasi-Mansat R; Souffreau J; Callaerts-Vegh Z; Van Nuffelen A; Moons L; D'Hooge R; Lupu F; Carmeliet P; Collen D; Dewerchin M Arterioscler Thromb Vasc Biol; 2011 Dec; 31(12):2881-8. PubMed ID: 21940951 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]