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73篇 您的检索式：作者名="Terwindt"

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	题名	作者	年代	出处	被引量
1	A gene for a new monogenic neurovascular migraine syndrome:a next step in unravelling molecular pathways for migraine显示文摘	Vanmolkol KR Terwindt GM Frants RR et a1	2008	Cephalalgia2008，28，5：	1
2	Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+channel gene CACNL1A4显示文摘	Ophoff RA Terwindt GM Vergouwe MN	1996	Cell1996，87，3：	1
3	Migraine:gene mutation and functional consequences显示文摘	Van den Maagdenberg AM Haan J Terwindt GM	2007	Curr Opin Neurol2007，20，3：	1
4	Familial hemilegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNLI A4显示文摘	Terwindt GM Vergouwe MN	1996	Cell1996，57，：	1
5	Interpretation of NOTCH3 mutations in the diagnosis of CADASIL显示文摘	Rutten JW Haan J Terwindt GM	2014	Expert Rev Mol Diagn2014，14，5：	1
6	Migraine:a complex genetic disorder显示文摘	Wessman M Terwindt GM Kaunisto MA	2007	Lancet Neurol2007，6，6：	1
7	Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2~ channel gene CACNL1A4显示文摘	Ophoff RA Terwindt GM Vergouwe MN	1996	Cell1996，87，3：	1
8	Structural brain changes in migraine显示文摘	Palm-Meinders IH Koppen H Terwindt GM		0，，：	1
9	Migraine and MTH-FR C677T genotype in a population-based sample显示文摘	Scher AI Terwindt GM Verschuren WM	2006	Ann Neu-rol2006，59，2：	1
10	Migraine and MTH- FR C677T genotype in a population-based sample 显示文摘	Scher AI Terwindt GM Verschuren WM	2006	Ann Neurol2006，59，2：	1
11	Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca^2+ channel gene显示文摘	Ophoff RA Terwindt GM Vergouwe MN	1996	CACNLIA4 Ce111996，87，3：	1
12	Headache and epilepsy 显示文摘	Bauer PR Carpay JA Terwindt GM	2013	Curr Pain Headache Rep2013，17，：	1
13	The impact of migraine on quality of life in the general population: the GEM study显示文摘	Terwindt GM Ferrari MD Tijhuis M	2000	Neurology2000，55，5：	1
14	Genetics of migraine 显示文摘	] Haan J Terwindt GM Ferrari MD	1997	Neurol Clin1997，15，：	1
15	Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca^2+ channel gene CACNL1A4显示文摘	Ophoff RA Terwindt GM Vergouwe MN	1996	Cell1996，87，3：	1
16	Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy,migraine and Raynaud's phenomenon显示文摘	GM Terwindt J Haan RA Ophoff SM Groenen CW Storimans JB Lanser RA Roos EM Bleeker-Wagemakers RR Frants and MD Ferrari	1998	Brain Vol 121 Issue 2:303-3161998，，：	1
17	Cardiovascular risk factors and migraine:the GEM population-based study显示文摘	Scher AI Terwindt GM Picavet HS	2005	Neurology2005，64，：	1
18	Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutation in the Ca2 + channel' gene CACNA1A 显示文摘	Ophoff R A Terwindt G M Vergouwe M N	1996	Cell1996，87，3：	1
19	A review of the genetic relation between migraine and epilepsy 显示文摘	Haan J Terwindt GM van den Maagden- berg AM	2008	Cephalalgia2008，28，：	1
20	The prevalence and charL acteristics of migraine in a populati-based cohort: GEM study显示文摘	Launer LJ Terwindt GM Ferrari MD	1999	Neurology1999，53，3：	1

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