Wszolek ZK - Search Results

1

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.

Theuns J, Verstraeten A, Sleegers K, Wauters E, Gijselinck I, Smolders S, Crosiers D, Corsmit E, Elinck E, Sharma M, Krüger R, Lesage S, Brice A, Chung SJ, Kim MJ, Kim YJ, Ross OA, Wszolek ZK, Rogaeva E, Xi Z, Lang AE, Klein C, Weissbach A, Mellick GD, Silburn PA, Hadjigeorgiou GM, Dardiotis E, Hattori N, Ogaki K, Tan EK, Zhao Y, Aasly J, Valente EM, Petrucci S, Annesi G, Quattrone A, Ferrarese C, Brighina L, Deutschländer A, Puschmann A, Nilsson C, Garraux G, LeDoux MS, Pfeiffer RF, Boczarska-Jedynak M, Opala G, Maraganore DM, Engelborghs S, De Deyn PP, Cras P, Cruts M, Van Broeckhoven C; GEO-PD Consortium. Theuns J, et al. Among authors: wszolek zk. Neurology. 2014 Nov 18;83(21):1906-13. doi: 10.1212/WNL.0000000000001012. Epub 2014 Oct 17. Neurology. 2014. PMID: 25326098 Free PMC article.

2

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration.

Wszolek ZK, Pfeiffer RF, Bhatt MH, Schelper RL, Cordes M, Snow BJ, Rodnitzky RL, Wolters EC, Arwert F, Calne DB. Wszolek ZK, et al. Ann Neurol. 1992 Sep;32(3):312-20. doi: 10.1002/ana.410320303. Ann Neurol. 1992. PMID: 1416801

3

Genetic considerations in movement disorders.

Wszolek ZK, Pfeiffer RF. Wszolek ZK, et al. Curr Opin Neurol Neurosurg. 1992 Jun;5(3):324-30. Curr Opin Neurol Neurosurg. 1992. PMID: 1623259 Review.

4

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

5

Western Nebraska family (family D) with autosomal dominant parkinsonism.

Wszolek ZK, Pfeiffer B, Fulgham JR, Parisi JE, Thompson BM, Uitti RJ, Calne DB, Pfeiffer RF. Wszolek ZK, et al. Neurology. 1995 Mar;45(3 Pt 1):502-5. doi: 10.1212/wnl.45.3.502. Neurology. 1995. PMID: 7898705

6

Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes.

Gasser T, Wszolek ZK, Trofatter J, Ozelius L, Uitti RJ, Lee CS, Gusella J, Pfeiffer RF, Calne DB, Breakefield XO. Gasser T, et al. Among authors: wszolek zk. Ann Neurol. 1994 Sep;36(3):387-96. doi: 10.1002/ana.410360310. Ann Neurol. 1994. PMID: 7915897

7

Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration family.

Kishore A, Wszolek ZK, Snow BJ, de la Fuente-Fernandez R, Arwert F, Wijker M, Schulzer M, Calne DB, Vingerhoets FJ. Kishore A, et al. Among authors: wszolek zk. Neurology. 1996 Dec;47(6):1588-90. doi: 10.1212/wnl.47.6.1588. Neurology. 1996. PMID: 8960754

8

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

9

Familial parkinsonism, dementia, and Lewy body disease: study of family G.

Denson MA, Wszolek ZK, Pfeiffer RF, Wszolek EK, Paschall TM, McComb RD. Denson MA, et al. Among authors: wszolek zk, wszolek ek. Ann Neurol. 1997 Oct;42(4):638-43. doi: 10.1002/ana.410420415. Ann Neurol. 1997. PMID: 9382476

10

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

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