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PARK8 LRRK2 parkinsonism.
Haugarvoll K, Wszolek ZK. Haugarvoll K, et al. Among authors: wszolek zk. Curr Neurol Neurosci Rep. 2006 Jul;6(4):287-94. doi: 10.1007/s11910-006-0020-0. Curr Neurol Neurosci Rep. 2006. PMID: 16822348 Review.
LRRK2 gene and tremor-dominant parkinsonism.
Haugarvoll K, Uitti RJ, Farrer MJ, Wszolek ZK. Haugarvoll K, et al. Among authors: wszolek zk. Arch Neurol. 2006 Sep;63(9):1346-7. doi: 10.1001/archneur.63.9.1346-b. Arch Neurol. 2006. PMID: 16966525 No abstract available.
Clinical features of LRRK2 parkinsonism.
Haugarvoll K, Wszolek ZK. Haugarvoll K, et al. Among authors: wszolek zk. Parkinsonism Relat Disord. 2009 Dec;15 Suppl 3:S205-8. doi: 10.1016/S1353-8020(09)70815-6. Parkinsonism Relat Disord. 2009. PMID: 20082991 Review.
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
Haugarvoll K, Rademakers R, Kachergus JM, Nuytemans K, Ross OA, Gibson JM, Tan EK, Gaig C, Tolosa E, Goldwurm S, Guidi M, Riboldazzi G, Brown L, Walter U, Benecke R, Berg D, Gasser T, Theuns J, Pals P, Cras P, De Deyn PP, Engelborghs S, Pickut B, Uitti RJ, Foroud T, Nichols WC, Hagenah J, Klein C, Samii A, Zabetian CP, Bonifati V, Van Broeckhoven C, Farrer MJ, Wszolek ZK. Haugarvoll K, et al. Among authors: wszolek zk. Neurology. 2008 Apr 15;70(16 Pt 2):1456-60. doi: 10.1212/01.wnl.0000304044.22253.03. Epub 2008 Mar 12. Neurology. 2008. PMID: 18337586 Free PMC article.
ELAVL4, PARK10, and the Celts.
Haugarvoll K, Toft M, Ross OA, Stone JT, Heckman MG, White LR, Lynch T, Gibson JM, Wszolek ZK, Uitti RJ, Aasly JO, Farrer MJ. Haugarvoll K, et al. Among authors: wszolek zk. Mov Disord. 2007 Mar 15;22(4):585-7. doi: 10.1002/mds.21336. Mov Disord. 2007. PMID: 17230446
Phactr2 and Parkinson's disease.
Wider C, Lincoln SJ, Heckman MG, Diehl NN, Stone JT, Haugarvoll K, Aasly JO, Gibson JM, Lynch T, Rajput A, Rajput ML, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA. Wider C, et al. Among authors: wszolek zk. Neurosci Lett. 2009 Mar 27;453(1):9-11. doi: 10.1016/j.neulet.2009.02.009. Epub 2009 Feb 10. Neurosci Lett. 2009. PMID: 19429005 Free PMC article.
Genomewide association, Parkinson disease, and PARK10.
Farrer MJ, Haugarvoll K, Ross OA, Stone JT, Milkovic NM, Cobb SA, Whittle AJ, Lincoln SJ, Hulihan MM, Heckman MG, White LR, Aasly JO, Gibson JM, Gosal D, Lynch T, Wszolek ZK, Uitti RJ, Toft M. Farrer MJ, et al. Among authors: wszolek zk. Am J Hum Genet. 2006 Jun;78(6):1084-8; author reply 1092-4. doi: 10.1086/504728. Am J Hum Genet. 2006. PMID: 16685661 Free PMC article. No abstract available.
The genetics of frontotemporal dementia.
Haugarvoll K, Wszolek ZK, Hutton M. Haugarvoll K, et al. Among authors: wszolek zk. Neurol Clin. 2007 Aug;25(3):697-715, vi. doi: 10.1016/j.ncl.2007.03.002. Neurol Clin. 2007. PMID: 17659186 Review.
Reported mutations in GIGYF2 are not a common cause of Parkinson's disease.
Vilariño-Güell C, Ross OA, Soto AI, Farrer MJ, Haugarvoll K, Aasly JO, Uitti RJ, Wszolek ZK. Vilariño-Güell C, et al. Among authors: wszolek zk. Mov Disord. 2009 Mar 15;24(4):619-20. doi: 10.1002/mds.22451. Mov Disord. 2009. PMID: 19133664 No abstract available.
701 results