Similar articles for PMID: 8878478

Year	Number of Results
1995	1
1996	1
1997	3
1998	1
1999	2
2000	6
2001	12
2002	8
2003	6
2004	13
2005	9
2006	3
2007	5
2008	5
2009	3
2010	3
2011	6
2012	2
2013	2
2014	4
2015	7
2016	2
2017	1
2018	1
2020	1
2021	2
2022	1
2024	0

1

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.

Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Nature. 1996 Oct 24;383(6602):707-10. doi: 10.1038/383707a0. Nature. 1996. PMID: 8878478

2

Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.

Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Maréchal E, Maciazek J, Vayssière C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Ann N Y Acad Sci. 1997 Sep 26;826:213-7. doi: 10.1111/j.1749-6632.1997.tb48472.x. Ann N Y Acad Sci. 1997. PMID: 9329692 Review.

3

CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia.

Kalimo H, Ruchoux MM, Viitanen M, Kalaria RN. Kalimo H, et al. Brain Pathol. 2002 Jul;12(3):371-84. doi: 10.1111/j.1750-3639.2002.tb00451.x. Brain Pathol. 2002. PMID: 12146805 Free PMC article. Review.

4

[From gene to disease; from Notch3 to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].

Oberstein SA, Bakker E, Ferrari MD, Haan J. Oberstein SA, et al. Ned Tijdschr Geneeskd. 2001 Feb 24;145(8):359-60. Ned Tijdschr Geneeskd. 2001. PMID: 11257815 Review. Dutch.

5

An animal model for the molecular genetics of CADASIL. (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy).

Fryxell KJ, Soderlund M, Jordan TV. Fryxell KJ, et al. Stroke. 2001 Jan;32(1):6-11. doi: 10.1161/01.str.32.1.6. Stroke. 2001. PMID: 11136906

6

Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.

Santa Y, Uyama E, Chui DH, Arima M, Kotorii S, Takahashi K, Tabira T. Santa Y, et al. J Neurol Sci. 2003 Aug 15;212(1-2):79-84. doi: 10.1016/s0022-510x(03)00109-6. J Neurol Sci. 2003. PMID: 12810003

7

Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Ruchoux MM, Domenga V, Brulin P, Maciazek J, Limol S, Tournier-Lasserve E, Joutel A. Ruchoux MM, et al. Am J Pathol. 2003 Jan;162(1):329-42. doi: 10.1016/S0002-9440(10)63824-2. Am J Pathol. 2003. PMID: 12507916 Free PMC article.

8

[NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].

Wang ZX, Lu H, Zhang Y, Bu DF, Niu XY, Zhang Z, Huang YN, Yuan Y. Wang ZX, et al. Zhonghua Yi Xue Za Zhi. 2004 Jul 17;84(14):1175-80. Zhonghua Yi Xue Za Zhi. 2004. PMID: 15387979 Chinese.

9

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Lesnik Oberstein SA, Haan J. Lesnik Oberstein SA, et al. Panminerva Med. 2004 Dec;46(4):265-76. Panminerva Med. 2004. PMID: 15876982 Review.

10

Acute unilateral visual loss as the first symptom of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Rufa A, De Stefano N, Dotti MT, Bianchi S, Sicurelli F, Stromillo ML, D'Aniello B, Federico A. Rufa A, et al. Arch Neurol. 2004 Apr;61(4):577-80. doi: 10.1001/archneur.61.4.577. Arch Neurol. 2004. PMID: 15096408

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