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Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.
Wray S, Self M; NINDS Parkinson's Disease iPSC Consortium; NINDS Huntington's Disease iPSC Consortium; NINDS ALS iPSC Consortium; Lewis PA, Taanman JW, Ryan NS, Mahoney CJ, Liang Y, Devine MJ, Sheerin UM, Houlden H, Morris HR, Healy D, Marti-Masso JF, Preza E, Barker S, Sutherland M, Corriveau RA, D'Andrea M, Schapira AH, Uitti RJ, Guttman M, Opala G, Jasinska-Myga B, Puschmann A, Nilsson C, Espay AJ, Slawek J, Gutmann L, Boeve BF, Boylan K, Stoessl AJ, Ross OA, Maragakis NJ, Van Gerpen J, Gerstenhaber M, Gwinn K, Dawson TM, Isacson O, Marder KS, Clark LN, Przedborski SE, Finkbeiner S, Rothstein JD, Wszolek ZK, Rossor MN, Hardy J. Wray S, et al. Among authors: puschmann a. PLoS One. 2012;7(8):e43099. doi: 10.1371/journal.pone.0043099. Epub 2012 Aug 27. PLoS One. 2012. PMID: 22952635 Free PMC article.
Diagnosing Monogenic Stroke at Younger Age.
Ilinca A, Kafantari E, Wallenius J, Kristoffersson U, Englund E, Puschmann A, Lindgren AG. Ilinca A, et al. Among authors: puschmann a. Stroke. 2024 Dec;55(12):2846-2855. doi: 10.1161/STROKEAHA.124.048044. Epub 2024 Nov 5. Stroke. 2024. PMID: 39498567
Is GBA1 T369M not a risk factor for Parkinson's disease in the Swedish population?
Brolin KA, Bäckström D, Wallenius J, Gan-Or Z, Puschmann A, Hansson O, Swanberg M. Brolin KA, et al. Among authors: puschmann a. medRxiv [Preprint]. 2024 Mar 16:2024.03.15.24304347. doi: 10.1101/2024.03.15.24304347. medRxiv. 2024. Update in: Parkinsonism Relat Disord. 2025 Jan;130:107191. doi: 10.1016/j.parkreldis.2024.107191 PMID: 38559109 Free PMC article. Updated. Preprint.
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.
LRRK2 variation and Parkinson's disease in African Americans.
Ross OA, Wilhoite GJ, Bacon JA, Soto-Ortolaza A, Kachergus J, Cobb SA, Puschmann A, Vilariño-Güell C, Farrer MJ, Graff-Radford N, Meschia JF, Wszolek ZK. Ross OA, et al. Among authors: puschmann a. Mov Disord. 2010 Sep 15;25(12):1973-6. doi: 10.1002/mds.23163. Mov Disord. 2010. PMID: 20669299 Free PMC article.
Diagnosis and treatment of common forms of tremor.
Puschmann A, Wszolek ZK. Puschmann A, et al. Semin Neurol. 2011 Feb;31(1):65-77. doi: 10.1055/s-0031-1271312. Epub 2011 Feb 14. Semin Neurol. 2011. PMID: 21321834 Free PMC article. Review.
Human leukocyte antigen variation and Parkinson's disease.
Puschmann A, Verbeeck C, Heckman MG, Soto-Ortolaza AI, Lynch T, Jasinska-Myga B, Opala G, Krygowska-Wajs A, Barcikowska M, Uitti RJ, Wszolek ZK, Ross OA. Puschmann A, et al. Parkinsonism Relat Disord. 2011 Jun;17(5):376-8. doi: 10.1016/j.parkreldis.2011.03.008. Epub 2011 Apr 11. Parkinsonism Relat Disord. 2011. PMID: 21482477 Free PMC article.
An African-American family with dystonia.
Puschmann A, Xiao J, Bastian RW, Searcy JA, LeDoux MS, Wszolek ZK. Puschmann A, et al. Parkinsonism Relat Disord. 2011 Aug;17(7):547-50. doi: 10.1016/j.parkreldis.2011.04.019. Epub 2011 May 20. Parkinsonism Relat Disord. 2011. PMID: 21601506 Free PMC article.
126 results