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Results: 1 to 20 of 634

1.
2.

Migraine and white matter hyperintensities.

Porter A, Gladstone JP, Dodick DW.

Curr Pain Headache Rep. 2005 Aug;9(4):289-93. Review.

PMID:
16004847
[PubMed - indexed for MEDLINE]
4.

Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Chabriat H, Vahedi K, Iba-Zizen MT, Joutel A, Nibbio A, Nagy TG, Krebs MO, Julien J, Dubois B, Ducrocq X, et al.

Lancet. 1995 Oct 7;346(8980):934-9.

PMID:
7564728
[PubMed - indexed for MEDLINE]
5.

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
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

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

Ueda M, Nakaguma R, Ando Y.

Rinsho Byori. 2009 Mar;57(3):242-51. Review. Japanese.

PMID:
19363995
[PubMed - indexed for MEDLINE]
8.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): a case report with review of literature.

Gurumukhani JK, Ursekar M, Singhal BS.

Neurol India. 2004 Mar;52(1):99-101.

PMID:
15069251
[PubMed - indexed for MEDLINE]
Free Article
9.

Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL.

Viswanathan A, Gschwendtner A, Guichard JP, Buffon F, Cumurciuc R, O'Sullivan M, Holtmannspötter M, Pachai C, Bousser MG, Dichgans M, Chabriat H.

Neurology. 2007 Jul 10;69(2):172-9.

PMID:
17620550
[PubMed - indexed for MEDLINE]
10.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy without anterior temporal pole involvement: a case report.

Kobayashi J, Sato S, Okumura K, Miyashita F, Ueda A, Ando Y, Toyoda K.

J Stroke Cerebrovasc Dis. 2014 Mar;23(3):e241-2. doi: 10.1016/j.jstrokecerebrovasdis.2013.10.013. Epub 2013 Dec 2.

PMID:
24295602
[PubMed - indexed for MEDLINE]
11.

Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Miao Q, Paloneva T, Tuominen S, Pöyhönen M, Tuisku S, Viitanen M, Kalimo H.

Brain Pathol. 2004 Oct;14(4):358-64.

PMID:
15605982
[PubMed - indexed for MEDLINE]
12.

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
[PubMed - indexed for MEDLINE]
13.

Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients.

Pantoni L, Pescini F, Nannucci S, Sarti C, Bianchi S, Dotti MT, Federico A, Inzitari D.

Neurology. 2010 Jan 5;74(1):57-63. doi: 10.1212/WNL.0b013e3181c7da7c.

PMID:
20038773
[PubMed - indexed for MEDLINE]
14.

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
[PubMed - indexed for MEDLINE]
15.

Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

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

J Neurol Sci. 2005 Feb 15;228(2):125-8. Epub 2004 Dec 24.

PMID:
15694192
[PubMed - indexed for MEDLINE]
16.

SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia only.

Mellies JK, Bäumer T, Müller JA, Tournier-Lasserve E, Chabriat H, Knobloch O, Hackelöer HJ, Goebel HH, Wetzig L, Haller P.

Neurology. 1998 Jun;50(6):1715-21.

PMID:
9633716
[PubMed - indexed for MEDLINE]
17.

[A new Spanish family with CADASIL associated with 346C>T mutation of NOTCH3 gene].

Avila A, Bello J, Maho P, Gómez MI.

Neurologia. 2007 Sep;22(7):484-7. Spanish.

PMID:
17853970
[PubMed - indexed for MEDLINE]
18.

CADASIL.

Hervé D, Chabriat H.

J Geriatr Psychiatry Neurol. 2010 Dec;23(4):269-76. doi: 10.1177/0891988710383570. Review.

PMID:
21045164
[PubMed - indexed for MEDLINE]
19.

[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging].

Chabriat H, Joutel A, Vahedi K, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG.

Bull Acad Natl Med. 2000;184(7):1523-31; discussion 1531-3. Review. French.

PMID:
11261256
[PubMed - indexed for MEDLINE]
20.

Lacunar infarcts are the main correlate with cognitive dysfunction in CADASIL.

Liem MK, van der Grond J, Haan J, van den Boom R, Ferrari MD, Knaap YM, Breuning MH, van Buchem MA, Middelkoop HA, Lesnik Oberstein SA.

Stroke. 2007 Mar;38(3):923-8. Epub 2007 Feb 1.

PMID:
17272761
[PubMed - indexed for MEDLINE]
Free Article
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