First report of an Iraqi Kurdish CADASIL patient.

作者信息

Mignarri Andrea, Martini Giuseppe, Malandrini Alessandro, Bellini Matteo, Bianchi Silvia, Tassi Rossana, Federico Antonio, Dotti Maria Teresa

出版信息

Neurol Sci. 2011 Apr;32(2):359-60. doi: 10.1007/s10072-010-0399-x. Epub 2010 Sep 21.

DOI:10.1007/s10072-010-0399-x

PMID:20857162

Abstract

摘要

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First report of an Iraqi Kurdish CADASIL patient.

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引用本文的文献

Imaging characteristics of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Bosn J Basic Med Sci. 2015 Feb 9;15(1):1-8. doi: 10.17305/bjbms.2015.247.

De novo mutation in the NOTCH3 gene causing CADASIL.

Bosn J Basic Med Sci. 2014 Feb;14(1):48-50. doi: 10.17305/bjbms.2014.2297.

本文引用的文献

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.

Brain. 2009 Apr;132(Pt 4):933-9. doi: 10.1093/brain/awn364. Epub 2009 Jan 27.

Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Stroke. 2007 Feb;38(2):276-80. doi: 10.1161/01.STR.0000254530.38417.07. Epub 2007 Jan 11.

SYMPTOMATIC OCCULT HYDROCEPHALUS WITH "NORMAL" CEREBROSPINAL-FLUID PRESSURE. A TREATABLE SYNDROME.

N Engl J Med. 1965 Jul 15;273:117-26. doi: 10.1056/NEJM196507152730301.

Diagnostic strategies in CADASIL.

Neurology. 2002 Oct 22;59(8):1134-8. doi: 10.1212/wnl.59.8.1134.

Patterns of MRI lesions in CADASIL.

Neurology. 1998 Aug;51(2):452-7. doi: 10.1212/wnl.51.2.452.

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients.

Lancet. 1997 Nov 22;350(9090):1511-5. doi: 10.1016/S0140-6736(97)08083-5.

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.

Nature. 1996 Oct 24;383(6602):707-10. doi: 10.1038/383707a0.

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相似文献

First report of an Iraqi Kurdish CADASIL patient.

Neurol Sci. 2011 Apr;32(2):359-60. doi: 10.1007/s10072-010-0399-x. Epub 2010 Sep 21.

Cysteine-sparing notch3 mutations: cadasil or cadasil variants?

Neurology. 2008 Sep 2;71(10):774-6. doi: 10.1212/01.wnl.0000324928.44694.f7.

Report of two Chinese families and a review of Mainland Chinese CADASIL patients.

J Neurol Sci. 2009 Apr 15;279(1-2):88-92. doi: 10.1016/j.jns.2008.12.011. Epub 2009 Jan 23.

CADASIL with a novel NOTCH3 mutation (Cys478Tyr).

J Stroke Cerebrovasc Dis. 2015 Mar;24(3):e61-2. doi: 10.1016/j.jstrokecerebrovasdis.2014.11.022. Epub 2015 Jan 13.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a patient from Sri Lanka.

J Clin Neurosci. 2009 Nov;16(11):1492-3. doi: 10.1016/j.jocn.2009.01.019. Epub 2009 Aug 15.

A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient.

J Neurol Sci. 2008 Apr 15;267(1-2):170-3. doi: 10.1016/j.jns.2007.10.017. Epub 2007 Nov 19.

An unusual case of elderly-onset cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with multiple cerebrovascular risk factors.

J Stroke Cerebrovasc Dis. 2012 Feb;21(2):143-5. doi: 10.1016/j.jstrokecerebrovasdis.2010.05.008. Epub 2010 Sep 19.

Unusual clinical presentations in subjects carrying novel NOTCH3 gene mutations.

J Stroke Cerebrovasc Dis. 2013 May;22(4):539-44. doi: 10.1016/j.jstrokecerebrovasdis.2013.02.002. Epub 2013 Mar 1.

CADASIL with Multiorgan Involvement: a Complete Autopsy Examination Report.

Can J Neurol Sci. 2016 Jan;43(1):202-5. doi: 10.1017/cjn.2015.240. Epub 2015 Jul 3.

Epilepsy in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Cerebrovasc Dis. 2007;24(2-3):316-7. doi: 10.1159/000106518. Epub 2007 Aug 3.

引用本文的文献

Imaging characteristics of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Bosn J Basic Med Sci. 2015 Feb 9;15(1):1-8. doi: 10.17305/bjbms.2015.247.

De novo mutation in the NOTCH3 gene causing CADASIL.

Bosn J Basic Med Sci. 2014 Feb;14(1):48-50. doi: 10.17305/bjbms.2014.2297.

本文引用的文献

Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients.

Brain. 2009 Apr;132(Pt 4):933-9. doi: 10.1093/brain/awn364. Epub 2009 Jan 27.

Cardiac autonomic nervous system and risk of arrhythmias in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Stroke. 2007 Feb;38(2):276-80. doi: 10.1161/01.STR.0000254530.38417.07. Epub 2007 Jan 11.

SYMPTOMATIC OCCULT HYDROCEPHALUS WITH "NORMAL" CEREBROSPINAL-FLUID PRESSURE. A TREATABLE SYNDROME.

N Engl J Med. 1965 Jul 15;273:117-26. doi: 10.1056/NEJM196507152730301.

Diagnostic strategies in CADASIL.

Neurology. 2002 Oct 22;59(8):1134-8. doi: 10.1212/wnl.59.8.1134.

Patterns of MRI lesions in CADASIL.

Neurology. 1998 Aug;51(2):452-7. doi: 10.1212/wnl.51.2.452.

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients.

Lancet. 1997 Nov 22;350(9090):1511-5. doi: 10.1016/S0140-6736(97)08083-5.

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.

Nature. 1996 Oct 24;383(6602):707-10. doi: 10.1038/383707a0.