Wszolek ZK - Search Results

1

Severe vascular disturbance in a case of familial brain calcinosis.

Miklossy J, Mackenzie IR, Dorovini-Zis K, Calne DB, Wszolek ZK, Klegeris A, McGeer PL. Miklossy J, et al. Among authors: wszolek zk. Acta Neuropathol. 2005 Jun;109(6):643-53. doi: 10.1007/s00401-005-1007-7. Epub 2005 Jun 4. Acta Neuropathol. 2005. PMID: 15937691

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

[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.

4

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

5

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

6

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.

7

SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings.

Furtado S, Farrer M, Tsuboi Y, Klimek ML, de la Fuente-Fernández R, Hussey J, Lockhart P, Calne DB, Suchowersky O, Stoessl AJ, Wszolek ZK. Furtado S, et al. Among authors: wszolek zk. Neurology. 2002 Nov 26;59(10):1625-7. doi: 10.1212/01.wnl.0000035625.19871.dc. Neurology. 2002. PMID: 12451209 Clinical Trial.

8

The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.

Zimprich A, Müller-Myhsok B, Farrer M, Leitner P, Sharma M, Hulihan M, Lockhart P, Strongosky A, Kachergus J, Calne DB, Stoessl J, Uitti RJ, Pfeiffer RF, Trenkwalder C, Homann N, Ott E, Wenzel K, Asmus F, Hardy J, Wszolek Z, Gasser T. Zimprich A, et al. Am J Hum Genet. 2004 Jan;74(1):11-9. doi: 10.1086/380647. Epub 2003 Dec 19. Am J Hum Genet. 2004. PMID: 14691730 Free PMC article.

9

Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).

Furtado S, Payami H, Lockhart PJ, Hanson M, Nutt JG, Singleton AA, Singleton A, Bower J, Utti RJ, Bird TD, de la Fuente-Fernandez R, Tsuboi Y, Klimek ML, Suchowersky O, Hardy J, Calne DB, Wszolek ZK, Farrer M, Gwinn-Hardy K, Stoessl AJ. Furtado S, et al. Among authors: wszolek zk. Mov Disord. 2004 Jun;19(6):622-9. doi: 10.1002/mds.20074. Mov Disord. 2004. PMID: 15197699 Review.

10

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. Arch Neurol. 2004 Jul;61(7):1057-60. doi: 10.1001/archneur.61.7.1057. Arch Neurol. 2004. PMID: 15262735

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