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Items: 10

1.

Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients.

Opherk C, Peters N, Herzog J, Luedtke R, Dichgans M.

Brain. 2004 Nov;127(Pt 11):2533-9. Epub 2004 Sep 13.

PMID:
15364702
2.

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

Lesnik Oberstein SA, Haan J.

Panminerva Med. 2004 Dec;46(4):265-76. Review.

PMID:
15876982
3.

The spectrum of mutations for CADASIL diagnosis.

Federico A, Bianchi S, Dotti MT.

Neurol Sci. 2005 Jun;26(2):117-24. Review.

PMID:
15995828
4.

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.

Ann N Y Acad Sci. 1997 Sep 26;826:213-7. Review.

PMID:
9329692
5.

The pathogenesis of CADASIL: an update.

Kalaria RN, Viitanen M, Kalimo H, Dichgans M, Tabira T; CADASIL Group of Vas-Cog.

J Neurol Sci. 2004 Nov 15;226(1-2):35-9. Review.

PMID:
15537516
6.

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

Kalimo H, Ruchoux MM, Viitanen M, Kalaria RN.

Brain Pathol. 2002 Jul;12(3):371-84. Review.

PMID:
12146805
7.

[Diagnosis, pathomechanism and treatment of CADASIL].

Mizuno T.

Rinsho Shinkeigaku. 2012;52(5):303-13. Review. Japanese.

PMID:
22688109
8.

[CADASIL syndrome - cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].

Dziewulska D, Kwieciński H.

Neurol Neurochir Pol. 2008 Mar-Apr;42(2):123-30. Review. Polish.

PMID:
18512169
9.

CADASIL: hereditary arteriopathy leading to multiple brain infarcts and dementia.

Viitanen M, Kalimo H.

Ann N Y Acad Sci. 2000 Apr;903:273-84. Review.

PMID:
10818516
10.

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

Oberstein SA, Bakker E, Ferrari MD, Haan J.

Ned Tijdschr Geneeskd. 2001 Feb 24;145(8):359-60. Review. Dutch.

PMID:
11257815

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