Wszolek Z - Search Results

1

First appraisal of brain pathology owing to A30P mutant alpha-synuclein.

Seidel K, Schöls L, Nuber S, Petrasch-Parwez E, Gierga K, Wszolek Z, Dickson D, Gai WP, Bornemann A, Riess O, Rami A, Den Dunnen WF, Deller T, Rüb U, Krüger R. Seidel K, et al. Among authors: wszolek z. Ann Neurol. 2010 May;67(5):684-9. doi: 10.1002/ana.21966. Ann Neurol. 2010. PMID: 20437567

2

Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.

Kobayashi H, Krüger R, Markopoulou K, Wszolek Z, Chase B, Taka H, Mineki R, Murayama K, Riess O, Mizuno Y, Hattori N. Kobayashi H, et al. Among authors: wszolek z. Brain. 2003 Jan;126(Pt 1):32-42. doi: 10.1093/brain/awg010. Brain. 2003. PMID: 12477695

3

Atrophy of superior cerebellar peduncle in progressive supranuclear palsy.

Tsuboi Y, Slowinski J, Josephs KA, Honer WG, Wszolek ZK, Dickson DW. Tsuboi Y, et al. Among authors: wszolek zk. Neurology. 2003 Jun 10;60(11):1766-9. doi: 10.1212/01.wnl.0000068011.21396.f4. Neurology. 2003. PMID: 12796528

4

Tau pathology in the olfactory bulb correlates with Braak stage, Lewy body pathology and apolipoprotein epsilon4.

Tsuboi Y, Wszolek ZK, Graff-Radford NR, Cookson N, Dickson DW. Tsuboi Y, et al. Among authors: wszolek zk. Neuropathol Appl Neurobiol. 2003 Oct;29(5):503-10. doi: 10.1046/j.1365-2990.2003.00453.x. Neuropathol Appl Neurobiol. 2003. PMID: 14507342

5

Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.

Farrer M, Kachergus J, Forno L, Lincoln S, Wang DS, Hulihan M, Maraganore D, Gwinn-Hardy K, Wszolek Z, Dickson D, Langston JW. Farrer M, et al. Among authors: wszolek z. Ann Neurol. 2004 Feb;55(2):174-9. doi: 10.1002/ana.10846. Ann Neurol. 2004. PMID: 14755720

6

Autosomal dominant parkinsonism associated with variable synuclein and tau pathology.

Wszolek ZK, Pfeiffer RF, Tsuboi Y, Uitti RJ, McComb RD, Stoessl AJ, Strongosky AJ, Zimprich A, Müller-Myhsok B, Farrer MJ, Gasser T, Calne DB, Dickson DW. Wszolek ZK, et al. Neurology. 2004 May 11;62(9):1619-22. doi: 10.1212/01.wnl.0000125015.06989.db. Neurology. 2004. PMID: 15136696

7

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.

Zimprich A, Biskup S, Leitner P, Lichtner P, Farrer M, Lincoln S, Kachergus J, Hulihan M, Uitti RJ, Calne DB, Stoessl AJ, Pfeiffer RF, Patenge N, Carbajal IC, Vieregge P, Asmus F, Müller-Myhsok B, Dickson DW, Meitinger T, Strom TM, Wszolek ZK, Gasser T. Zimprich A, et al. Neuron. 2004 Nov 18;44(4):601-7. doi: 10.1016/j.neuron.2004.11.005. Neuron. 2004. PMID: 15541309 Free article.

8

Frontotemporal dementia and parkinsonism linked to chromosome 17.

Wszołek ZK, Słowiński J, Golan M, Dickson DW. Wszołek ZK, et al. Folia Neuropathol. 2005;43(4):258-70. Folia Neuropathol. 2005. PMID: 16416390 Free article. Review.

9

Lrrk2 and Lewy body disease.

Ross OA, Toft M, Whittle AJ, Johnson JL, Papapetropoulos S, Mash DC, Litvan I, Gordon MF, Wszolek ZK, Farrer MJ, Dickson DW. Ross OA, et al. Ann Neurol. 2006 Feb;59(2):388-93. doi: 10.1002/ana.20731. Ann Neurol. 2006. PMID: 16437559

10

Absence of rapid eye movement sleep behavior disorder in 11 members of the pallidopontonigral degeneration kindred.

Boeve BF, Lin SC, Strongosky A, Dickson DW, Wszolek ZK. Boeve BF, et al. Arch Neurol. 2006 Feb;63(2):268-72. doi: 10.1001/archneur.63.2.268. Arch Neurol. 2006. PMID: 16476816

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

723 results

Search Page

Filters