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79篇 您的检索式：作者名="Zimprich"

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	题名	作者	年代	出处	被引量
1	Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome显示文摘	Zimprich A Grabowski M Asmus F	2001	Nat Genet2001，29，1：	1
2	Cross-sectionally and longitudinally balanced effects of processing speed on intellectual abilities显示文摘	Zimprich D		0，，03：	1
3	Real-time measurements of calcium dynamics in neurons developing in situ within zebrafish embryos显示文摘	Zimprich F Ashworth R Bolsover S	1998	Pflugers Arch1998，436，：	1
4	The clinical impact of pharmacogenetics on the treatment of epilepsy 显示文摘	Loscher W Klotz U Zimprich F	2009	Epilepsia2009，50，1：	1
5	Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder 显示文摘	Zimprich A Hatala K Riederer F	2008	Psychiatr Genet2008，18，6：	1
6	Real-time measurements of calcium dynamics in neurons developing insitu within zebrafish ernbryos显示文摘	Zimprich F Ashworth R Bolsover S	1998	Pflugers Arch1998，436，3：	1
7	Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pa- thology 显示文摘	Zimprich A Biskup S Leitner P	2004	Neuron2004，44，4：	1
8	Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleontorphic pathology显示文摘	Zimprich A Biskup S Leitner P et M	2004	Neuron2004，44，4：	1
9	The clinical impact of pharmaco- genetics on the treatment of epilepsy 显示文摘	Loscher W Klotz U Zimprich F	2009	Epilepsia2009，50，1：	1
10	An allelic variation in the human prodynorphin gene promoter alters stimulus-induced expression显示文摘	Zimprich A Kraus J Woltje M	2000	J Neurochem2000，74，2：	1
11	Mutations in LRRK2 cause autosomal dominant parkinsonism with pleomorphic pathology显示文摘	Zimprich A Biskup S Leitner P	2004	Neuron2004，44，4：	1
12	The clinical impact of pharmacogenetics on the treatment of epilepsy 显示文摘	Loscher W Klotz U Zimprich F	2009	Epilepsia2009，50，：	1
13	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
14	Size effects in small scaled lead-free solder joints 显示文摘	Zimprich P Betzwar-Kotas A Khatibi G	2008	Journal of Materials Science: Materials in Elec- tronics2008，19，4：	1
15	Myoclonus-dystonia syndrome:epsilon-sarcoglycan mutations and phenotype显示文摘	Asmus F Zimprich A Tezenas Du Montcel S	2002	Ann Neurol2002，52，：	1
16	The sepiapterin reductase gene region reveals association in the PARK3 locus:analysis of familial and sporadic Parkinson's disease in European populations显示文摘	Sharma M Mueller JC Zimprich A	2006	J Med Genet2006，43，7：	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	A Mutation in VPS35 , Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson Disease显示文摘	Alexander Zimprich Anna Benet-Pagès Walter Struhal Elisabeth Graf Sebastian H. Eck Marc N. Offman Dietrich Haubenberger Sabine Spielberger Eva C. Schulte Peter Lichtner Shaila C. Rossle Norman Klopp Elisabeth Wolf Klaus Seppi Walter Pirker Stefan Presslau	2011	The American Journal of Human Genetics2011，，1：	1
19	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
20	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

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