Wszolek ZK - Search Results

1

FTDP-17 with Pick body-like inclusions associated with a novel tau mutation, p.E372G.

Tacik P, DeTure MA, Carlomagno Y, Lin WL, Murray ME, Baker MC, Josephs KA, Boeve BF, Wszolek ZK, Graff-Radford NR, Parisi JE, Petrucelli L, Rademakers R, Isaacson RS, Heilman KM, Petersen RC, Dickson DW, Kouri N. Tacik P, et al. Among authors: wszolek zk. Brain Pathol. 2017 Sep;27(5):612-626. doi: 10.1111/bpa.12428. Epub 2016 Oct 5. Brain Pathol. 2017. PMID: 27529406 Free PMC article.

2

Phenotypic correlations in FTDP-17.

Reed LA, Wszolek ZK, Hutton M. Reed LA, et al. Among authors: wszolek zk. Neurobiol Aging. 2001 Jan-Feb;22(1):89-107. doi: 10.1016/s0197-4580(00)00202-5. Neurobiol Aging. 2001. PMID: 11164280 Review.

3

Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation.

Wszolek ZK, Tsuboi Y, Uitti RJ, Reed L, Hutton ML, Dickson DW. Wszolek ZK, et al. Brain. 2001 Aug;124(Pt 8):1666-70. doi: 10.1093/brain/124.8.1666. Brain. 2001. PMID: 11459757 No abstract available.

4

Recent advances in the understanding of tau protein and movement disorders.

Arvanitakis Z, Wszolek ZK. Arvanitakis Z, et al. Among authors: wszolek zk. Curr Opin Neurol. 2001 Aug;14(4):491-7. doi: 10.1097/00019052-200108000-00010. Curr Opin Neurol. 2001. PMID: 11470966 Review.

5

Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonism.

Wszolek ZK, Gwinn-Hardy K, Wszolek EK, Muenter MD, Pfeiffer RF, Rodnitzky RL, Uitti RJ, McComb RD, Gasser T, Dickson DW. Wszolek ZK, et al. Among authors: wszolek ek. Acta Neuropathol. 2002 Apr;103(4):344-50. doi: 10.1007/s00401-001-0474-8. Epub 2001 Dec 8. Acta Neuropathol. 2002. PMID: 11904753

6

Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.

Tsuboi Y, Uitti RJ, Delisle MB, Ferreira JJ, Brefel-Courbon C, Rascol O, Ghetti B, Murrell JR, Hutton M, Baker M, Wszolek ZK. Tsuboi Y, et al. Among authors: wszolek zk. Arch Neurol. 2002 Jun;59(6):943-50. doi: 10.1001/archneur.59.6.943. Arch Neurol. 2002. PMID: 12056930

7

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17).

Tsuboi Y, Baker M, Hutton ML, Uitti RJ, Rascol O, Delisle MB, Soulages X, Murrell JR, Ghetti B, Yasuda M, Komure O, Kuno S, Arima K, Sunohara N, Kobayashi T, Mizuno Y, Wszolek ZK. Tsuboi Y, et al. Among authors: wszolek zk. Neurology. 2002 Dec 10;59(11):1791-3. doi: 10.1212/01.wnl.0000038909.49164.4b. Neurology. 2002. PMID: 12473774

8

Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17.

Cheshire WP, Tsuboi Y, Wszolek ZK. Cheshire WP, et al. Among authors: wszolek zk. Auton Neurosci. 2002 Nov 29;102(1-2):71-7. doi: 10.1016/s1566-0702(02)00205-9. Auton Neurosci. 2002. PMID: 12492138

9

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

Tsuboi Y, Uitti RJ, Baker M, Hutton ML, Wszolek ZK. Tsuboi Y, et al. Among authors: wszolek zk. Neurology. 2003 Feb 11;60(3):525-6. doi: 10.1212/wnl.60.3.525-b. Neurology. 2003. PMID: 12578950 No abstract available.

10

[Japanese contribution to the understanding of frontotemporal dementia and parkinsonism linked to chromosome 17(FTDP-17)].

Tsuboi Y, Wszolek ZK, Mizuno Y, Kobayashi T, Yasuda M, Yamada T. Tsuboi Y, et al. Among authors: wszolek zk. No To Shinkei. 2003 Feb;55(2):107-19. No To Shinkei. 2003. PMID: 12684990 Review. Japanese.

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