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Items: 1 to 20 of 39

1.
2.

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
3.

CADASIL: a monogenic condition causing stroke and subcortical vascular dementia.

Dichgans M.

Cerebrovasc Dis. 2002;13 Suppl 2:37-41. Review.

PMID:
11901241
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.

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

PMID:
11257815
5.

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
6.

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
7.

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
8.

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

Chen YC, Hsiao CT, Soong BW, Lee YC.

Acta Neurol Taiwan. 2014 Jun;23(2):64-74. Review. Chinese.

9.
10.

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

Otori T, Katayama Y.

Nihon Rinsho. 2004 Jan;62 Suppl:331-4. Review. Japanese. No abstract available.

PMID:
15011378
11.

[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
12.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Guidetti D, Casali B, Mazzei RL, Dotti MT.

Clin Exp Hypertens. 2006 Apr-May;28(3-4):271-7. Review.

PMID:
16833034
13.

CADASIL and genetics of cerebral ischaemia.

Kalaria RN, Low WC, Oakley AE, Slade JY, Ince PG, Morris CM, Mizuno T.

J Neural Transm Suppl. 2002;(63):75-90. Review.

PMID:
12597610
14.

Notch signaling and CADASIL.

Tang SC, Jeng JS, Lee MJ, Yip PK.

Acta Neurol Taiwan. 2009 Jun;18(2):81-90. Review.

PMID:
19673359
15.

The spectrum of mutations for CADASIL diagnosis.

Federico A, Bianchi S, Dotti MT.

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

PMID:
15995828
16.

Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families.

Thomas NJ, Morris CM, Scaravilli F, Johansson J, Rossor M, De Lange R, St Clair D, Nicoll J, Blank C, Coulthard A, Bushby K, Ince PG, Burn D, Kalaria RN.

Ann N Y Acad Sci. 2000 Apr;903:293-8. Review.

PMID:
10818518
17.

CADASIL: experimental insights from animal models.

Ayata C.

Stroke. 2010 Oct;41(10 Suppl):S129-34. doi: 10.1161/STROKEAHA.110.595207. Review.

18.

[Study of the familiar form of vascular dementia (CADASIL)].

Takahashi K, Yoshizaki K.

Nihon Shinkei Seishin Yakurigaku Zasshi. 2007 Jun;27(3):141-5. Review. Japanese.

PMID:
17633526
19.

[Dominant autosomal cerebral arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). A review].

Navarro E, Díaz F, Muñoz L, Giménez-Roldán S.

Neurologia. 2002 Oct;17(8):410-7. Review. Spanish.

PMID:
12396971
20.

[Molecular basis and physiopathogenic mechanisms of CADASIL: a model of small vessel diseases of the brain].

Joutel A, Tournier-Lasserve E.

J Soc Biol. 2002;196(1):109-15. Review. French.

PMID:
12134625

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