维普期刊资源整合服务平台（V6.5）

38篇 您的检索式：作者名="Eunson"

选中清除导出查看参考文献查看引证文献引用追踪共2页首页上一页第1页下一页末页 /2 跳转

	题名	作者	年代	出处	被引量
1	P250 Central nervous system (CNS) complications of ear nose throat (ENT) infections – case series显示文摘	N. Vora P.D. Eunson K.K. Tallur A. Baxter R.A. Minns A.J.W. Steers L. Myles A.E. McLellan	2009	European Journal of Paediatric Neurology2009，，：	2
2	Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1 associated with epilepsy 显示文摘	Spauschus A Eunson L Hanna MG	1999	Ann NYAcadSci1999，868，3：	1
3	Clinical, genetic,and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability 显示文摘	Eunson LH Rea R Zuberi SM	2000	Ann Neurol2000，48，4：	1
4	Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel显示文摘	Eunson LH Spauschus A	2001	Lancet2001，358，：	1
5	Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel显示文摘	Jouvenceau A Eunson L Spauschus A	2001	Lancet2001，358，9284：	1
6	Late-onset episodic ataxia type 2 due to an in-frame insertion in CACNA1A显示文摘	Imbrici P Eunson L H Graves T D	2005	Neurology2005，65，6：	1
7	P250 Central nervous system (CNS) complications of ear nose throat(ENT) infections-case series显示文摘	Vora N Eunson P D Tallur K K	2009	European Jonr?alofPaedi?tricNenr?logy2009，13，1：	1
8	Sodium channel gene mutations inhypokalaemic periodic paralysis: an uncommon cause in the UK显示文摘	Davies NP Eunson LH Samuel M	2001	Neurology2001，57，：	1
9	Expanding the phenotype of potassium channelopathy:severe neuromyotonia and skeletal deformities without prominent episodic ataxia显示文摘	Kinali M Jungbluth H Eunson LH	2004	Neuromuscul Disord2004，14，10：	1
10	Clinical,genetic,and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability显示文摘	Eunson LH Rea R Zuberi SM	2000	Ann Neurol2000，48，：	1
11	Human epi- lepsy associated with dysfunction of the brain P/Q-type calci- um channel显示文摘	Jouveneeau A Eunson L H Spausehus A	2001	The Lancet2001，358，9284：	1
12	The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS 显示文摘	PULKES T EUNSON L PATTERSON V	1999	Ann Neurol1999，46，6：	1
13	Functional characterization of a novel mutation in KCNA1 in episodic ataxia type 1associated with epiiepsy显示文摘	Spauschus A Eunson L Hanna MG	1999	Ann N Y Acad Sci1999，868，：	1
14	Sodium channel gene mutations in hypokalemic periodic paralysis: an uncommon cause in the UK显示文摘	Davies NP Eunson LH Samuel M	2001	Neurology2001，57，7：	1
15	Sodium channel gene mutations inbypokalaemic periodic paralysis: anuncommon cause in the UK显示文摘	Davies NP Eunson LH Samuel M	2001	Neurology2001，57，：	1
16	New calcium channel mutations predict aberrant RNA splicing in episodic ataxia显示文摘	Eunson LH Graves TD Hanna MG	2005	Neurology2005，65，：	1
17	Sodium channel gene muta- tions in hypokalemic periodic paralysis : an uncommon cause in the UK 显示文摘	Davies NP Eunson LH Samuel M	2001	Neurology2001，57，7：	1
18	Spasticity in children and young people with non-progressive brain disorders:summary of NICE guidance显示文摘	Mugglestone MA Eunson P Murphy MS	2012	BMJ2012，，345：	1
19	Aetiology and epidemiology of cerebral palsy 显示文摘	Eunson P	2012	Paediatrics and Child Health2012，22，9：	1
20	Sodium channel gene mutations in hypokalemic periodic paralysis:an uncommon cause in the UK显示文摘	Davies NP Eunson LH Samuel	2001	Neurology2001，57，7：	1

返回顶部每页显示：

共2页首页上一页第1页下一页末页 /2 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示