Wszolek ZK - Search Results

1

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease).

Oliveira JR, Spiteri E, Sobrido MJ, Hopfer S, Klepper J, Voit T, Gilbert J, Wszolek ZK, Calne DB, Stoessl AJ, Hutton M, Manyam BV, Boller F, Baquero M, Geschwind DH. Oliveira JR, et al. Among authors: wszolek zk. Neurology. 2004 Dec 14;63(11):2165-7. doi: 10.1212/01.wnl.0000145601.88274.88. Neurology. 2004. PMID: 15596772

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

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

4

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

5

[Hereditary Parkinson disease: report of 3 families with dominant autosomal inheritance].

Wszolek ZK, Cordes M, Calne DB, Münter MD, Cordes I, Pfeifer RF. Wszolek ZK, et al. Nervenarzt. 1993 May;64(5):331-5. Nervenarzt. 1993. PMID: 8321342 German.

6

Genetic linkage studies in autosomal dominantly inherited L-DOPA responsive parkinsonism. Evaluation of candidate genes.

Gasser T, Wszolek Z, Supala A, Trofatter J, Ozelius L, Uitti RJ, Pfeiffer RF, Gusella J, Calne D, Breakefield XO. Gasser T, et al. Adv Neurol. 1996;69:87-95. Adv Neurol. 1996. PMID: 8615189 Clinical Trial. No abstract available.

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

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD. Gasser T, et al. Among authors: wszolek zk. Nat Genet. 1998 Mar;18(3):262-5. doi: 10.1038/ng0398-262. Nat Genet. 1998. PMID: 9500549

10

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17.

Clark LN, Poorkaj P, Wszolek Z, Geschwind DH, Nasreddine ZS, Miller B, Li D, Payami H, Awert F, Markopoulou K, Andreadis A, D'Souza I, Lee VM, Reed L, Trojanowski JQ, Zhukareva V, Bird T, Schellenberg G, Wilhelmsen KC. Clark LN, et al. Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13103-7. doi: 10.1073/pnas.95.22.13103. Proc Natl Acad Sci U S A. 1998. PMID: 9789048 Free PMC article.

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