Wszolek Z - Search Results

1

Clustering of Parkinson disease: shared cause or coincidence?

Kumar A, Calne SM, Schulzer M, Mak E, Wszolek Z, Van Netten C, Tsui JK, Stoessl AJ, Calne DB. Kumar A, et al. Among authors: wszolek z. Arch Neurol. 2004 Jul;61(7):1057-60. doi: 10.1001/archneur.61.7.1057. Arch Neurol. 2004. PMID: 15262735

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. Among authors: wszolek z. 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

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

9

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

10

Positron emission tomography in pallido-ponto-nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene).

Pal PK, Wszolek ZK, Kishore A, de la Fuente-Fernandez R, Sossi V, Uitti RJ, Dobko T, Stoessl AJ. Pal PK, et al. Among authors: wszolek zk. Parkinsonism Relat Disord. 2001 Apr;7(2):81-88. doi: 10.1016/s1353-8020(00)00026-2. Parkinsonism Relat Disord. 2001. PMID: 11248587

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

722 results

Search Page

Filters