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21篇 您的检索式：作者名="KACHERGUS"

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	题名	作者	年代	出处	被引量
1	LRRK2 pathogenic substitutions in Parkinson's disease显示文摘	Mata IF Kachergus JM Taylor JP	2005	Neurogenetics2005，6，：	1
2	Lrrk2 pathogenic substitutions in Parkinson's disease显示文摘	Mata IF Kachergus JM Taylor JP	2005	Neurogenetics2005，6，4：	1
3	Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications 显示文摘	FARRER M KACHERGUS J FOMO L	2004	Ann Neurol2004，55，2：	1
4	Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication 显示文摘	Fuchs J Nilsson C Kachergus J	2007	Neurology2007，68，12：	1
5	Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication 显示文摘	Fuchs J Nilsson C Kachergus J	2007	Neu- rology2007，68，：	1
6	Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations显示文摘	Kachergus J Mata IF Hulihan M	2005	Am J Hum Genet2005，76，4：	1
7	Alpha-synuclein locus dupilincation as a cause of familial Parkinson's disease显示文摘	Chartier-Harlin MC Kachergus J Roumier C	2004	Lancet2004，364，：	1
8	Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication显示文摘	Fuchs J Nilsson C Kachergus J	2007	Neu- rology2007，68，：	1
9	Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: Evidence of a common founder across European populations 显示文摘	Kachergus J Mata 117 Hulihan M	2005	American Journal of Human Genetics2005，76，4：	1
10	Identification of a novel LRRK2 mutation linked to autosomal dominant Parkinsonism:Evidence of a common founder across European populations显示文摘	Kachergus J Mata IF Hulian M	2005	Am J Hum Genet2005，76，：	1
11	Alpha-synuclein locus duplication as a cause of familial Parkinson' s disease显示文摘	Chartier-Harlin MC Kachergus J Roumier C	2004	Lancet2004，364，9440：	1
12	Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology显示文摘	Alexander Zimprich Saskia Biskup Petra Leitner Peter Lichtner Matthew Farrer Sarah Lincoln Jennifer Kachergus Mary Hulihan Ryan J. Uitti Donald B. Calne A.Jon Stoessl Ronald F. Pfeiffer Nadja Patenge Iria Carballo Carbajal Peter Vieregge Friedrich Asmus B	2004	Neuron2004，，4：	1
13	DCTN1 mutations in Perry syndrome显示文摘	Farrer MJ Hulihan MM Kachergus JM	2009	Nat Genet2009，41，：	1
14	Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease显示文摘	Haugarvoll K Rademakers R Kachergus JM	2008	Neurology2008，70，162：	1
15	Alpha-synuclein locus duplication as a cause of familialParkinson,s disease 显示文摘	Chartier-Harlin MC Kachergus J Roumier C	2004	Lancet2004，364，9440：	1
16	Comparison of kin- dreds with parkinsonism and alpha-synuclein genomic mul- tiplications显示文摘	Farrer M Kachergus J Fomo L	2004	Ann Neuro12004，55，2：	1
17	Alpha-synuclein locus duplication as a cause of familial Parkinson's disease显示文摘	Chartier-Harlin MC Kachergus J lincoln S	2004	Lancet2004，364，：	1
18	alpha-Synuclein locus triplication causes Parkinson's disease显示文摘	Singleton AB Farrer M Kachergus J	2003	Science2003，302，：	1
19	Alpha-synuclein locus duplication as a cause of familial Parkinson′s disease显示文摘	CHARTIER HARLIN M C KACHERGUS J ROUMIER C		0，，9440：	1
20	Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication显示文摘	FUCHS J NILSSON C KACHERGUS J		0，，12：	1

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