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SCA2 family presenting as typical Parkinson's disease: 34 year follow up.
Kim YE, Jeon B, Farrer MJ, Scott E, Guella I, Park SS, Kim JM, Park HY, Kim A, Son YD, Cho ZH. Kim YE, et al. Among authors: farrer mj. Parkinsonism Relat Disord. 2017 Jul;40:69-72. doi: 10.1016/j.parkreldis.2017.04.003. Epub 2017 Apr 12. Parkinsonism Relat Disord. 2017. PMID: 28462804
A family with a tau P301L mutation presenting with parkinsonism.
Walker RH, Friedman J, Wiener J, Hobler R, Gwinn-Hardy K, Adam A, DeWolfe J, Gibbs R, Baker M, Farrer M, Hutton M, Hardy J. Walker RH, et al. Parkinsonism Relat Disord. 2002 Dec;9(2):121-3. doi: 10.1016/s1353-8020(02)00003-2. Parkinsonism Relat Disord. 2002. PMID: 12473404
Sporadic SCA8 mutation resembling corticobasal degeneration.
Baba Y, Uitti RJ, Farrer MJ, Wszolek ZK. Baba Y, et al. Among authors: farrer mj. Parkinsonism Relat Disord. 2005 May;11(3):147-50. doi: 10.1016/j.parkreldis.2004.10.008. Parkinsonism Relat Disord. 2005. PMID: 15823478
Genetic factors influencing age at onset in LRRK2-linked Parkinson disease.
Golub Y, Berg D, Calne DB, Pfeiffer RF, Uitti RJ, Stoessl AJ, Wszolek ZK, Farrer MJ, Mueller JC, Gasser T, Fuchs J. Golub Y, et al. Among authors: farrer mj. Parkinsonism Relat Disord. 2009 Aug;15(7):539-41. doi: 10.1016/j.parkreldis.2008.10.008. Epub 2008 Nov 28. Parkinsonism Relat Disord. 2009. PMID: 19041274
A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction.
Puschmann A, Ross OA, Vilariño-Güell C, Lincoln SJ, Kachergus JM, Cobb SA, Lindquist SG, Nielsen JE, Wszolek ZK, Farrer M, Widner H, van Westen D, Hägerström D, Markopoulou K, Chase BA, Nilsson K, Reimer J, Nilsson C. Puschmann A, et al. Parkinsonism Relat Disord. 2009 Nov;15(9):627-32. doi: 10.1016/j.parkreldis.2009.06.007. Epub 2009 Jul 25. Parkinsonism Relat Disord. 2009. PMID: 19632874 Free PMC article.
449 results