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Variation in GIGYF2 is not associated with Parkinson disease.
Neurology. 2009 Jun 2;72(22):1886-92. doi: 10.1212/01.wnl.0000346517.98982.1b. Epub 2009 Mar 11.
Neurology. 2009.
PMID: 19279319
Free PMC article.
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.
Nichols WC, Elsaesser VE, Pankratz N, Pauciulo MW, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T; Parkinson Study Group-PROGENI Investigators.
Nichols WC, et al. Among authors: elsaesser ve.
Neurology. 2007 Oct 30;69(18):1737-44. doi: 10.1212/01.wnl.0000278115.50741.4e. Epub 2007 Sep 5.
Neurology. 2007.
PMID: 17804834
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Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset.
Nichols WC, Pankratz N, Marek DK, Pauciulo MW, Elsaesser VE, Halter CA, Rudolph A, Wojcieszek J, Pfeiffer RF, Foroud T; Parkinson Study Group-PROGENI Investigators.
Nichols WC, et al. Among authors: elsaesser ve.
Neurology. 2009 Jan 27;72(4):310-6. doi: 10.1212/01.wnl.0000327823.81237.d1. Epub 2008 Nov 5.
Neurology. 2009.
PMID: 18987351
Free PMC article.
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Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH; PSG-PROGENI and GenePD Investigators, Coordinators and Molecular Genetic Laboratories.
Pankratz N, et al.
Hum Genet. 2009 Jan;124(6):593-605. doi: 10.1007/s00439-008-0582-9. Epub 2008 Nov 6.
Hum Genet. 2009.
PMID: 18985386
Free PMC article.
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Alpha-synuclein and familial Parkinson's disease.
Pankratz N, Nichols WC, Elsaesser VE, Pauciulo MW, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Pfeiffer RF, Foroud T; Parkinson Study Group - PROGENI Investigators.
Pankratz N, et al. Among authors: elsaesser ve.
Mov Disord. 2009 Jun 15;24(8):1125-31. doi: 10.1002/mds.22524.
Mov Disord. 2009.
PMID: 19412953
Free PMC article.
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Genomewide association study for onset age in Parkinson disease.
Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T; PROGENI Investigators, Coordinators and Molecular Genetic Laboratories; GenePD Investigators, Coordinators and Molecular Genetic Laboratories.
Latourelle JC, et al.
BMC Med Genet. 2009 Sep 22;10:98. doi: 10.1186/1471-2350-10-98.
BMC Med Genet. 2009.
PMID: 19772629
Free PMC article.
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Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease.
Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T, Nichols WC; Parkinson Study Group-PROGENI Investigators.
Pankratz N, et al. Among authors: elsaesser ve.
Mov Disord. 2006 Dec;21(12):2257-60. doi: 10.1002/mds.21162.
Mov Disord. 2006.
PMID: 17078063
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Mutations in DJ-1 are rare in familial Parkinson disease.
Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Wojcieszek J, Rudolph A, Shults CW, Foroud T, Nichols WC; Parkinson Study Group - PROGENI Investigators.
Pankratz N, et al. Among authors: elsaesser ve.
Neurosci Lett. 2006 Nov 20;408(3):209-13. doi: 10.1016/j.neulet.2006.09.003. Epub 2006 Sep 25.
Neurosci Lett. 2006.
PMID: 16997464
Free PMC article.
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