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Page 1
Tracing Woody Guthrie and Huntington's disease.
Arévalo J, Wojcieszek J, Conneally PM. Arévalo J, et al. Among authors: wojcieszek j. Semin Neurol. 2001 Jun;21(2):209-23. doi: 10.1055/s-2001-15269. Semin Neurol. 2001. PMID: 11442329
Saccades in presymptomatic and early stages of Huntington disease.
Blekher T, Johnson SA, Marshall J, White K, Hui S, Weaver M, Gray J, Yee R, Stout JC, Beristain X, Wojcieszek J, Foroud T. Blekher T, et al. Among authors: wojcieszek j. Neurology. 2006 Aug 8;67(3):394-9. doi: 10.1212/01.wnl.0000227890.87398.c1. Epub 2006 Jul 19. Neurology. 2006. PMID: 16855205
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: wojcieszek j. 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.
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation.
Nichols WC, Marek DK, Pauciulo MW, Pankratz N, Halter CA, Rudolph A, Shults CW, Wojcieszek J, Foroud T; Parkinson Study Group - PROGENI Investigators. Nichols WC, et al. Among authors: wojcieszek j. Mov Disord. 2007 Jan 15;22(2):254-7. doi: 10.1002/mds.21233. Mov Disord. 2007. PMID: 17149721
Are cognitive changes progressive in prediagnostic HD?
Stout JC, Weaver M, Solomon AC, Queller S, Hui S, Johnson SA, Gray J, Beristain X, Wojcieszek J, Foroud T. Stout JC, et al. Among authors: wojcieszek j. Cogn Behav Neurol. 2007 Dec;20(4):212-8. doi: 10.1097/WNN.0b013e31815cfef8. Cogn Behav Neurol. 2007. PMID: 18091069
Visual perception in prediagnostic and early stage Huntington's disease.
O'Donnell BF, Blekher TM, Weaver M, White KM, Marshall J, Beristain X, Stout JC, Gray J, Wojcieszek JM, Foroud TM. O'Donnell BF, et al. Among authors: wojcieszek jm. J Int Neuropsychol Soc. 2008 May;14(3):446-53. doi: 10.1017/S1355617708080405. J Int Neuropsychol Soc. 2008. PMID: 18419843 Free PMC article.
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.
108 results