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46篇 您的检索式：作者名="ZIMPRICH A"

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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	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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 Nettrochem2000，74，2：	1
14	Mutations in LRRK2 cause autosomal-dominant Parkinsonism with polymorphic pathology显示文摘	Zimprich A Biskup S Leitner P	2004	Neuron2004，44，4：	1
15	Mutations in LRRK2 cause autosomal - dominant parkinsonism with pleomor- phic pathology显示文摘	ZIMPRICH A BISKUP S LEITNER P	2004	Neuron2004，44，4：	1
16	A mutation in VPS35, encoding a subunit of the retromer complex, causes late- onset Parkinson disease显示文摘	Zimprich A Benet-Pages A Struhal W	2011	Am J Hum Genet2011，89，1：	1
17	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	Psychiatric Genetics2008，18，6：	1
18	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
19	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
20	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

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