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Similar articles for PubMed (Select 12417361)

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.

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

Dichgans M.

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

PMID:
11901241
7.

[CADASIL: a case with clinical, radiological, histological and genetic diagnoses].

Posada IJ, García-Morales I, Martínez MA, Hoenicka J, Bermejo F.

Neurologia. 2003 May;18(4):229-33. Spanish.

PMID:
12721871
8.
9.

A CADASIL case with normal skin biopsy and without mutations in exons 3 and 4 of the Notch3 gene.

de Freitas GR, Miklossy J, Christen-Zäch S, Reichhart M, Bogousslavsky J.

J Neurol Sci. 2001 Dec 15;193(1):43-7.

PMID:
11718749
10.

CADASIL-associated Notch3 mutations have differential effects both on ligand binding and ligand-induced Notch3 receptor signaling through RBP-Jk.

Peters N, Opherk C, Zacherle S, Capell A, Gempel P, Dichgans M.

Exp Cell Res. 2004 Oct 1;299(2):454-64.

PMID:
15350543
11.

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.

Arch Neurol. 2004 Apr;61(4):577-80.

PMID:
15096408
12.

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
13.

CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor.

Utku U, Celik Y, Uyguner O, Yüksel-Apak M, Wollnik B.

Eur J Neurol. 2002 Jan;9(1):23-8.

PMID:
11784372
14.

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
15.

[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.

Zhonghua Yi Xue Za Zhi. 2004 Jul 17;84(14):1175-80. Chinese.

PMID:
15387979
16.

Two Japanese CADASIL families with a R141C mutation in the Notch3 gene.

Murakami T, Iwatsuki K, Hayashi T, Sato K, Matsubara E, Nagano I, Manabe Y, Shoji M, Abe K.

Intern Med. 2001 Nov;40(11):1144-8.

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18.

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.

Chuah TL, Tan KM, Flanagan S, Hyland V, Sullivan AA, Henderson R, MacMillan J, Lander C.

J Clin Neurosci. 2001 Sep;8(5):404-6. Erratum in: J Clin Neurosci. 2003 May;10(3):395. Tan, S M [corrected to Tan, K M].

PMID:
11535004
19.

No association between multiple sclerosis and the Notch3 gene responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Broadley SA, Sawcer SJ, Chataway SJ, Coraddu F, Coles A, Gray J, Roxburgh R, Clayton D, Compston DA.

J Neurol Neurosurg Psychiatry. 2001 Jul;71(1):97-9.

20.

Migraine with aura and white matter abnormalities: Notch3 mutation.

Ceroni M, Poloni TE, Tonietti S, Fabozzi D, Uggetti C, Frediani F, Simonetti F, Malaspina A, Alimonti D, Celano M, Ferrari M, Carrera P.

Neurology. 2000 May 9;54(9):1869-71.

PMID:
10802804
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