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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1946 1
1947 1
1983 2
1993 3
1995 1
1996 3
1997 3
1998 3
1999 5
2000 3
2001 4
2002 2
2003 2
2004 7
2005 3
2006 1
2007 2
2008 5
2009 3
2010 2
2011 3
2012 7
2013 4
2014 6
2015 5
2016 4
2017 7
2018 9
2019 7
2020 12
2021 10
2022 5
2023 1
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124 results
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Page 1
ATP1A3-Related Neurologic Disorders.
Brashear A, Sweadner KJ, Cook JF, Swoboda KJ, Ozelius L. Brashear A, et al. 2008 Feb 7 [updated 2018 Feb 22]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. 2008 Feb 7 [updated 2018 Feb 22]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2023. PMID: 20301294 Free Books & Documents. Review.
Commentary.
Brashear A. Brashear A. Mov Disord. 2013 Dec;28(14):1939. doi: 10.1002/mds.25774. Mov Disord. 2013. PMID: 24323532 No abstract available.
Spasticity.
Brashear A, Lambeth K. Brashear A, et al. Curr Treat Options Neurol. 2009 May;11(3):153-61. doi: 10.1007/s11940-009-0018-4. Curr Treat Options Neurol. 2009. PMID: 19364449
Population genomics in neglected malaria parasites.
Brashear AM, Cui L. Brashear AM, et al. Front Microbiol. 2022 Sep 8;13:984394. doi: 10.3389/fmicb.2022.984394. eCollection 2022. Front Microbiol. 2022. PMID: 36160257 Free PMC article. Review.
Saving neurology: Once more with feeling.
Schor NF, Brashear A. Schor NF, et al. Among authors: brashear a. Neurology. 2019 Dec 3;93(23):989-990. doi: 10.1212/WNL.0000000000008569. Epub 2019 Nov 5. Neurology. 2019. PMID: 31690683 No abstract available.
A Multi-center Genome-wide Association Study of Cervical Dystonia.
Sun YV, Li C, Hui Q, Huang Y, Barbano R, Rodriguez R, Malaty IA, Reich S, Bambarger K, Holmes K, Jankovic J, Patel NJ, Roze E, Vidailhet M, Berman BD, LeDoux MS, Espay AJ, Agarwal P, Pirio-Richardson S, Frank SA, Ondo WG, Saunders-Pullman R, Chouinard S, Natividad S, Berardelli A, Pantelyat AY, Brashear A, Fox SH, Kasten M, Krämer UM, Neis M, Bäumer T, Loens S, Borsche M, Zittel S, Maurer A, Gelderblom M, Volkmann J, Odorfer T, Kühn AA, Borngräber F, König IR, Cruchaga C, Cotton AC, Kilic-Berkmen G, Freeman A, Factor SA, Scorr L, Bremner JD, Vaccarino V, Quyyumi AA, Klein C, Perlmutter JS, Lohmann K, Jinnah HA. Sun YV, et al. Among authors: brashear a. Mov Disord. 2021 Dec;36(12):2795-2801. doi: 10.1002/mds.28732. Epub 2021 Jul 28. Mov Disord. 2021. PMID: 34320236 Free PMC article.
Rapid-onset dystonia-parkinsonism.
Dobyns WB, Ozelius LJ, Kramer PL, Brashear A, Farlow MR, Perry TR, Walsh LE, Kasarskis EJ, Butler IJ, Breakefield XO. Dobyns WB, et al. Among authors: brashear a. Neurology. 1993 Dec;43(12):2596-602. doi: 10.1212/wnl.43.12.2596. Neurology. 1993. PMID: 8255463
Distinct neurological disorders with ATP1A3 mutations.
Heinzen EL, Arzimanoglou A, Brashear A, Clapcote SJ, Gurrieri F, Goldstein DB, Jóhannesson SH, Mikati MA, Neville B, Nicole S, Ozelius LJ, Poulsen H, Schyns T, Sweadner KJ, van den Maagdenberg A, Vilsen B; ATP1A3 Working Group. Heinzen EL, et al. Among authors: brashear a. Lancet Neurol. 2014 May;13(5):503-14. doi: 10.1016/S1474-4422(14)70011-0. Lancet Neurol. 2014. PMID: 24739246 Free PMC article. Review.
ATP1A3 mutations: what is the phenotype?
Brashear A, Ozelius LJ, Sweadner KJ. Brashear A, et al. Neurology. 2014 Feb 11;82(6):468-9. doi: 10.1212/WNL.0000000000000113. Epub 2014 Jan 15. Neurology. 2014. PMID: 24431297 No abstract available.
124 results