Wszolek ZK - Search Results

1

A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction.

Puschmann A, Ross OA, Vilariño-Güell C, Lincoln SJ, Kachergus JM, Cobb SA, Lindquist SG, Nielsen JE, Wszolek ZK, Farrer M, Widner H, van Westen D, Hägerström D, Markopoulou K, Chase BA, Nilsson K, Reimer J, Nilsson C. Puschmann A, et al. Among authors: wszolek zk. Parkinsonism Relat Disord. 2009 Nov;15(9):627-32. doi: 10.1016/j.parkreldis.2009.06.007. Epub 2009 Jul 25. Parkinsonism Relat Disord. 2009. PMID: 19632874 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

Olfactory dysfunction in familial parkinsonism.

Markopoulou K, Larsen KW, Wszolek EK, Denson MA, Lang AE, Pfeiffer RF, Wszolek ZK. Markopoulou K, et al. Among authors: wszolek zk, wszolek ek. Neurology. 1997 Nov;49(5):1262-7. doi: 10.1212/wnl.49.5.1262. Neurology. 1997. PMID: 9371905

4

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD).

Vaughan JR, Farrer MJ, Wszolek ZK, Gasser T, Durr A, Agid Y, Bonifati V, DeMichele G, Volpe G, Lincoln S, Breteler M, Meco G, Brice A, Marsden CD, Hardy J, Wood NW. Vaughan JR, et al. Among authors: wszolek zk. Hum Mol Genet. 1998 Apr;7(4):751-3. doi: 10.1093/hmg/7.4.751. Hum Mol Genet. 1998. PMID: 9499430

5

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

6

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

7

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.

8

Positron emission tomography of dopamine pathways in familial Parkinsonian syndromes.

Pal PK, Wszolek ZK, Uitti R, Markopoulou K, Calne SM, Stoessl AJ, Calne DB. Pal PK, et al. Among authors: wszolek zk. Parkinsonism Relat Disord. 2001 Sep;8(1):51-6. doi: 10.1016/s1353-8020(01)00008-6. Parkinsonism Relat Disord. 2001. PMID: 11472880 Review.

9

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.

10

The human sideroflexin 5 (SFXN5) gene: sequence, expression analysis and exclusion as a candidate for PARK3.

Lockhart PJ, Holtom B, Lincoln S, Hussey J, Zimprich A, Gasser T, Wszolek ZK, Hardy J, Farrer MJ. Lockhart PJ, et al. Among authors: wszolek zk. Gene. 2002 Feb 20;285(1-2):229-37. doi: 10.1016/s0378-1119(02)00402-x. Gene. 2002. PMID: 12039050

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