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19篇 您的检索式：作者名="Stogmann"

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		题名	作者	年代	出处	被引量
	1	Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes 显示文摘	Stogmann E Lichtner P Baumgartner C	2006	Neurogenetics2006，7，4：	1
	2	Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes显示文摘	E Stogmann P Lichtner Baumgartner C	2006	Neurogenetics2006，7，4：	1
	3	A functional polymorphism in the prodynorphin gene promotor is associ-ated with temporal lobe epilepsy显示文摘	Stogmann E Zimprich A Baumgartner C	2002	Ann Neurol2002，51，2：	1
	4	Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy显示文摘	Zimprich F Sunder-Plassmann R Stogmann E	2004	Neurology2004，63，6：	1
	5	Association of an ABCB1 gene haplotype with pharmaeoresistanee in temporal lobe epilepsy显示文摘	Zimprich F Sunder-Plassman R Stogmann E	2004	Neurology2004，63，6：	1
	6	A functional polymorphism in the prodynorphin gene promoter is associated with temporal lobe epilepsy显示文摘	Stogmann E Zimprich A Baumgattner C	2002	Ann Neurol2002，51，2：	1
	7	Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilep- sy 显示文摘	Zimprich F Sunder-Plassmann R Stogmann E	2004	Neurology2004，63，6：	1
	8	Association of an ABCBI gene haploty- pe with pharmacoresistance in temporal lobe epilepsy 显示文摘	Zimprich F Sunder-Plassmann R Stogmann E	2004	Neurology2004，63，6：	1
	9	Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy显示文摘	Zimprich F Sunder-Plassmann R Stogmann E	2004	Neurology2004，63，6：	1
	10	Associa- tion of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy 显示文摘	Zimprich F Sunder-Plassmann R Stogmann E	2004	Neurology2004，63，6：	1
	11	A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures 显示文摘	Schlachter K Gruber-Sedlymar U Stogmann E	2009	Neurology2009，72，11：	1
	12	Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy 显示文摘	Zimprich F Sunder-Plassmann R Stogmann E Gleiss A Dal-Bianco A Zimprich A	2004	Neurology2004，63，6：	1
	13	A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures显示文摘	K Schlachter U Gruber-Sedlmayr E Stogmann M Lausecker C Hotzy J Balzar E Schuh C Baumgartner J C. Mueller T Illig H E. Wichmann P Lichtner T Meitinger T M. Strom A Zimprich F Zimprich	2009	Neurology2009，，11：	1
	14	A functional polymorphism in the SCN 1A gene is not associated with carbamazepine dosages in Austrian patients with epilepsy显示文摘	Zimprich F Stogmann E Bonelli S	2008	Epilepsia2008，49，6：	1
	15	Association of an ABCBI gene beplotype with pharmacoresistance in temporal lobe epilepsy显示文摘	Zimprich F Sunder-Plassmann R Stogmann E		Neurology0，63，3：	1
	16	A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures显示文摘	K Schlachter U Gruber-Sedlmayr E Stogmann M Lausecker C Hotzy J Balzar E Schuh C Baumgartner J C. Mueller T Illig H E. Wichmann P Lichtner T Meitinger T M. Strom A Zimprich F Zimprich	2009	Neurology2009，，11：	1
	17	Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsy显示文摘	Zimprich F Sunder-Plassmann R Stogmann E	2004	Neurology2004，63，6：	1
	18	Mutation in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes显示文摘	Stogmann E Lichtner P Baumgartner C	2006	Neurogenetics2006，7，4：	1
	19	Association of an ABCBI gene haplotype with pharmacoresistance in temporal lobe epilepsy显示文摘	Zimprich F Sunder-Plassmann R Stogmann E		0，，06：	1

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