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153篇 您的检索式：作者名="Joutel"

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	题名	作者	年代	出处	被引量
1	皮质下小血管病诊断的共识声明显示文摘血管性认知损害是用于描述一组涉及大血管和小血管的散发性和遗传性异质性疾病的诊断术语。皮质下小血管病可导致腔隙性梗死和进行性白质损害。被称为宾斯旺格病(Binswanger's disease, BD)的进行性白质损害患者构成了从单纯血管性疾病到合并神经变性病变的疾病谱。BD患者是一个相对同质性的亚组,存在缺氧缺血、腔隙性梗死和炎症,它们协同作用破坏血脑屏障和髓鞘。通过临床、脑脊液、神经心理学和影像学检查获得的多模式疾病标记物能促进该亚组患者的鉴别。本共识声明确定了一系列基于基础病理学改变的潜在生物学标记物,这将有助于诊断以及将来协作性治疗试验的患者选择。	Gary A Rosenberg Anders Wallin Joanna M Wardlaw Hugh S Markus Joan Montaner Leslie Wolfson Costantino Iadecola Berislav V Zlokovic Anne Joutel Martin Dichgans Marco Duering Reinhold Schmidt Amos D Korczyn Lea T Grinberg Helena C Chui Vladimir Hachinski 王训师张劼陈涵丰俞娅美徐子奇罗本燕	2016	国际脑血管病杂志2016，24，6：	18
2	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12 显示文摘	Tournler - Lasserve E Joutel A Melki J	1993	Nat C enet1993，3，：	1
3	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy map to chromosome 19q12显示文摘	Tourinier-Lasserve E Joutel A Meiki J	1993	Nature Genetics1993，3，3：	1
4	Notch 3 mutations in CADASIL, a hereditary adultonset condition causing stroke and dementia 显示文摘	Joutel A Corpechot C Ducros A	1996	Nature1996，383，：	1
5	The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel显示文摘	Ducros A Denier C Joutel A	2001	N Engl J Med2001，345，1：	1
6	Laparoscopic creation of a neovagina by Vecchiettib technique:anatomic and functional results 显示文摘	Abramowicz S Oden S Joutel N	2013	Gynecol Obstet Fertil2013，41，1：	1
7	A long-term numerical so- lution for the insolation quantities of the Eart显示文摘	Laskar J Robutel P Joutel F	2004	Astronomyand Astrophysics2004，428，：	1
8	The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients显示文摘	Joutel A Andreux F Gaulis S	2000	J Clin Invest2000，105，5：	1
9	Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL),a mendelian condition causing stroke and vascular dementia显示文摘	Joutel A Corpechot C Ducros A	1997	Ann N Y Acad Sci1997，826，1：	1
10	Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis显示文摘	Joutel A Favrole P Labauge P		0，，9298：	1
11	Notch3 mutations in CADA- SIL, a hereditary adult - onset condition causing stroke and dementia 显示文摘	Joutel A Corpechot C Ducros A	1996	Nature1996，383，6602：	1
12	Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia显示文摘	Joutel A Corpechot C Ducros A	1996	Nature1996，383，6602：	1
13	CADASIL 显示文摘	Chabriat H Joutel A Dichgans M	2009	Lancet Neurol2009，8，7：	1
14	Agene for famil- ial hemiplegie migraine maps to chromosome 19 显示文摘	Joutel A Bousser M G Biousse V	1993	Na- ture Genet1993，5，：	1
15	The clinical spectrum of familial hemiplegie mi- graine associated with mutations in a neuronal calcium channel 显示文摘	Dueros A Denire C Joutel A	2001	N Engl J Med2001，345，1：	1
16	Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients 显示文摘	Joutel A Vahedi K Corpechot C	1997	Lancet1997，350，9090：	1
17	Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease显示文摘	Joutel A Monet-Lepr(e)tre M Gosele C	2010	Clin Invest2010，120，2：	1
18	Notch signalling pathway and human diseases显示文摘	Joutel A Tournier-Lasserve E	1998	Semin Cell Dev Biol1998，，6：	1
19	Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12显示文摘	Joutel A Melki J	1993	Nat Genet1993，3，：	1
20	Notch3 mutations in CADASIL,a hereditary adult-onset condition causing stroke and dementia显示文摘	Corpechot C Ducros A	1996	Nature1996，383，：	1

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