Wszolek ZK - Search Results

1

Alpha-synuclein repeat variants and survival in Parkinson's disease.

Chung SJ, Biernacka JM, Armasu SM, Anderson K, Frigerio R, Aasly JO, Annesi G, Bentivoglio AR, Brighina L, Chartier-Harlin MC, Goldwurm S, Hadjigeorgiou G, Jasinska-Myga B, Jeon BS, Kim YJ, Krüger R, Lesage S, Markopoulou K, Mellick G, Morrison KE, Puschmann A, Tan EK, Crosiers D, Theuns J, Van Broeckhoven C, Wirdefeldt K, Wszolek ZK, Elbaz A, Maraganore DM; Genetic Epidemiology of Parkinson's Disease Consortium. Chung SJ, et al. Among authors: wszolek zk. Mov Disord. 2014 Jul;29(8):1053-7. doi: 10.1002/mds.25841. Epub 2014 Feb 27. Mov Disord. 2014. PMID: 24578302 Free PMC article.

2

A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation.

Markopoulou K, Wszolek ZK, Pfeiffer RF. Markopoulou K, et al. Among authors: wszolek zk. Ann Neurol. 1995 Sep;38(3):373-8. doi: 10.1002/ana.410380306. Ann Neurol. 1995. PMID: 7668822

3

Reduced expression of the G209A alpha-synuclein allele in familial Parkinsonism.

Markopoulou K, Wszolek ZK, Pfeiffer RF, Chase BA. Markopoulou K, et al. Among authors: wszolek zk. Ann Neurol. 1999 Sep;46(3):374-81. doi: 10.1002/1531-8249(199909)46:3<374::aid-ana13>3.0.co;2-9. Ann Neurol. 1999. PMID: 10482268

4

PET studies of parkinsonism associated with mutation in the alpha-synuclein gene.

Samii A, Markopoulou K, Wszolek ZK, Sossi V, Dobko T, Mak E, Calne DB, Stoessl AJ. Samii A, et al. Among authors: wszolek zk. Neurology. 1999 Dec 10;53(9):2097-102. doi: 10.1212/wnl.53.9.2097. Neurology. 1999. PMID: 10599788

5

Olfactory dysfunction in Parkinson's disease.

Wszolek ZK, Markopoulou K. Wszolek ZK, et al. Clin Neurosci. 1998;5(2):94-101. Clin Neurosci. 1998. PMID: 10785834 Review.

6

Familial Parkinson's disease and related conditions. Clinical genetics.

Wszolek ZK, Uitti RJ, Markopoulou K. Wszolek ZK, et al. Adv Neurol. 2001;86:33-43. Adv Neurol. 2001. PMID: 11553993 Review. No abstract available.

7

Identifying genetic factors in Parkinson disease.

Farrer M, Hardy J, Hutton M, Maraganore D, Tsuboi Y, Wszolek ZK. Farrer M, et al. Among authors: wszolek zk. JAMA. 2002 Feb 13;287(6):715-6. doi: 10.1001/jama.287.6.715-a. JAMA. 2002. PMID: 11851532 No abstract available.

8

Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.

Kobayashi H, Krüger R, Markopoulou K, Wszolek Z, Chase B, Taka H, Mineki R, Murayama K, Riess O, Mizuno Y, Hattori N. Kobayashi H, et al. Brain. 2003 Jan;126(Pt 1):32-42. doi: 10.1093/brain/awg010. Brain. 2003. PMID: 12477695

9

Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.

Farrer M, Kachergus J, Forno L, Lincoln S, Wang DS, Hulihan M, Maraganore D, Gwinn-Hardy K, Wszolek Z, Dickson D, Langston JW. Farrer M, et al. Ann Neurol. 2004 Feb;55(2):174-9. doi: 10.1002/ana.10846. Ann Neurol. 2004. PMID: 14755720

10

Parkinsonism, FXTAS, and FMR1 premutations.

Toft M, Aasly J, Bisceglio G, Adler CH, Uitti RJ, Krygowska-Wajs A, Lynch T, Wszolek ZK, Farrer MJ. Toft M, et al. Among authors: wszolek zk. Mov Disord. 2005 Feb;20(2):230-3. doi: 10.1002/mds.20297. Mov Disord. 2005. PMID: 15390127

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