Wszolek ZK - Search Results

1

Latent trait modeling of tau neuropathology in progressive supranuclear palsy.

Kouri N, Murray ME, Reddy JS, Serie DJ, Soto-Beasley A, Allen M, Carrasquillo MM, Wang X, Castanedes MC, Baker MC, Rademakers R, Uitti RJ, Graff-Radford NR, Wszolek ZK, Schellenberg GD, Crook JE, Ertekin-Taner N, Ross OA, Dickson DW. Kouri N, et al. Among authors: wszolek zk. Acta Neuropathol. 2021 May;141(5):667-680. doi: 10.1007/s00401-021-02289-0. Epub 2021 Feb 26. Acta Neuropathol. 2021. PMID: 33635380 Free PMC article.

2

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

Hong M, Zhukareva V, Vogelsberg-Ragaglia V, Wszolek Z, Reed L, Miller BI, Geschwind DH, Bird TD, McKeel D, Goate A, Morris JC, Wilhelmsen KC, Schellenberg GD, Trojanowski JQ, Lee VM. Hong M, et al. Science. 1998 Dec 4;282(5395):1914-7. doi: 10.1126/science.282.5395.1914. Science. 1998. PMID: 9836646

3

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

Wszolek ZK, Uitti RJ, Hutton M. Wszolek ZK, et al. Neurology. 2000 May 23;54(10):2028-30. doi: 10.1212/wnl.54.10.2028. Neurology. 2000. PMID: 10822460 No abstract available.

4

Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene.

Wszolek ZK, Tsuboi Y, Uitti RJ, Reed L. Wszolek ZK, et al. Neurology. 2000 Dec 26;55(12):1939. doi: 10.1212/wnl.55.12.1939. Neurology. 2000. PMID: 11134413 No abstract available.

5

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.

6

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.

7

Familial Parkinson's disease and related conditions. Clinical genetics.

Wszolek ZK, Uitti RJ, Markopoulou K. Wszolek ZK, et al. Adv Neurol. 2001;86:33-43. Adv Neurol. 2001. PMID: 11553993 Review. No abstract available.

8

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

9

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

10

Hereditary tauopathies and parkinsonism.

Wszolek ZK, Tsuboi Y, Farrer M, Uitti RJ, Hutton ML. Wszolek ZK, et al. Adv Neurol. 2003;91:153-63. Adv Neurol. 2003. PMID: 12442674 Review. No abstract available.

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