Uitti RJ - Search Results

1

Association study between multiple system atrophy and TREM2 p.R47H.

Ogaki K, Heckman MG, Koga S, Martens YA, Labbé C, Lorenzo-Betancor O, Walton RL, Soto AI, Vargas ER, Fujioka S, Uitti RJ, van Gerpen JA, Cheshire WP, Younkin SG, Wszolek ZK, Low PA, Singer W, Bu G, Dickson DW, Ross OA. Ogaki K, et al. Among authors: uitti rj. Neurol Genet. 2018 Aug 1;4(4):e257. doi: 10.1212/NXG.0000000000000257. eCollection 2018 Aug. Neurol Genet. 2018. PMID: 30109269 Free PMC article.

2

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. Among authors: uitti rj. Neurology. 1995 Mar;45(3 Pt 1):502-5. doi: 10.1212/wnl.45.3.502. Neurology. 1995. PMID: 7898705

3

No evidence for systemic oxidant stress in Parkinson's or Alzheimer's disease.

Ahlskog JE, Uitti RJ, Low PA, Tyce GM, Nickander KK, Petersen RC, Kokmen E. Ahlskog JE, et al. Among authors: uitti rj. Mov Disord. 1995 Sep;10(5):566-73. doi: 10.1002/mds.870100507. Mov Disord. 1995. PMID: 8552107

4

Levodopa and deprenyl treatment effects on peripheral indices of oxidant stress in Parkinson's disease.

Ahlskog JE, Uitti RJ, Low PA, Tyce GM, O'Brien JF, Nickander KK. Ahlskog JE, et al. Among authors: uitti rj. Neurology. 1996 Mar;46(3):796-801. doi: 10.1212/wnl.46.3.796. Neurology. 1996. PMID: 8618686

5

Widespread alterations of alpha-synuclein in multiple system atrophy.

Dickson DW, Liu W, Hardy J, Farrer M, Mehta N, Uitti R, Mark M, Zimmerman T, Golbe L, Sage J, Sima A, D'Amato C, Albin R, Gilman S, Yen SH. Dickson DW, et al. Am J Pathol. 1999 Oct;155(4):1241-51. doi: 10.1016/s0002-9440(10)65226-1. Am J Pathol. 1999. PMID: 10514406 Free PMC article.

6

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

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

7

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. Among authors: uitti rj. Neurology. 2000 Dec 26;55(12):1939. doi: 10.1212/wnl.55.12.1939. Neurology. 2000. PMID: 11134413 No abstract available.

8

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. Among authors: uitti rj. Brain. 2001 Aug;124(Pt 8):1666-70. doi: 10.1093/brain/124.8.1666. Brain. 2001. PMID: 11459757 No abstract available.

9

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

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

10

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: uitti rj. Acta Neuropathol. 2002 Apr;103(4):344-50. doi: 10.1007/s00401-001-0474-8. Epub 2001 Dec 8. Acta Neuropathol. 2002. PMID: 11904753

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