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Items: 1 to 20 of 297

1.

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
2.

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
3.

CADASIL: hereditary disease of arteries causing brain infarcts and dementia.

Kalimo H, Viitanen M, Amberla K, Juvonen V, Marttila R, Pöyhönen M, Rinne JO, Savontaus M, Tuisku S, Winblad B.

Neuropathol Appl Neurobiol. 1999 Aug;25(4):257-65. Review.

PMID:
10476042
4.

An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene.

Guidetti D, Casali B, Mazzei RL, Cenacchi G, De Berti G, Zuccoli G, Nicoli D, Conforti FL, Sprovieri T, Pasquinelli G, Brini M.

Neurol Sci. 2004 Feb;24(6):401-6.

PMID:
14767686
5.
6.

[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
7.
9.
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.

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

Dichgans M.

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

PMID:
11901241
12.

[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
13.

Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation.

Tuominen S, Juvonen V, Amberla K, Jolma T, Rinne JO, Tuisku S, Kurki T, Marttila R, Pöyhönen M, Savontaus ML, Viitanen M, Kalimo H.

Stroke. 2001 Aug;32(8):1767-74.

14.

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
15.

Cerebral hemodynamics and white matter hyperintensities in CADASIL.

van den Boom R, Lesnik Oberstein SA, Spilt A, Behloul F, Ferrari MD, Haan J, Westendorp RG, van Buchem MA.

J Cereb Blood Flow Metab. 2003 May;23(5):599-604.

PMID:
12771575
17.

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
18.

[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
19.

A novel NOTCH3 frameshift deletion and mitochondrial abnormalities in a patient with CADASIL.

Dotti MT, De Stefano N, Bianchi S, Malandrini A, Battisti C, Cardaioli E, Federico A.

Arch Neurol. 2004 Jun;61(6):942-5.

PMID:
15210536
20.

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

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