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

Year Number of Results
1991 1
1993 1
1996 1
1997 2
1998 1
2002 2
2003 2
2004 3
2005 1
2006 1
2007 2
2008 1
2009 4
2010 2
2011 3
2012 4
2013 8
2014 14
2015 15
2016 19
2017 14
2018 16
2019 12
2020 20
2021 25
2022 19
2023 6
2024 1

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Similar articles for PMID: 27378932

171 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, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2008 Feb 7 [updated 2018 Feb 22]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301294 Free Books & Documents. Review.
Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity.
Lazarov E, Hillebrand M, Schröder S, Ternka K, Hofhuis J, Ohlenbusch A, Barrantes-Freer A, Pardo LA, Fruergaard MU, Nissen P, Brockmann K, Gärtner J, Rosewich H. Lazarov E, et al. Neurobiol Dis. 2020 Sep;143:105012. doi: 10.1016/j.nbd.2020.105012. Epub 2020 Jul 10. Neurobiol Dis. 2020. PMID: 32653672 Free article.
ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum.
Salles PA, Mata IF, Brünger T, Lal D, Fernandez HH. Salles PA, et al. Front Neurol. 2021 Apr 1;12:637890. doi: 10.3389/fneur.2021.637890. eCollection 2021. Front Neurol. 2021. PMID: 33868146 Free PMC article. Review.
The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.
Tranebjærg L, Strenzke N, Lindholm S, Rendtorff ND, Poulsen H, Khandelia H, Kopec W, Lyngbye TJB, Hamel C, Delettre C, Bocquet B, Bille M, Owen HH, Bek T, Jensen H, Østergaard K, Möller C, Luxon L, Carr L, Wilson L, Rajput K, Sirimanna T, Harrop-Griffiths K, Rahman S, Vona B, Doll J, Haaf T, Bartsch O, Rosewich H, Moser T, Bitner-Glindzicz M. Tranebjærg L, et al. Hum Genet. 2018 Feb;137(2):111-127. doi: 10.1007/s00439-017-1862-z. Epub 2018 Jan 5. Hum Genet. 2018. PMID: 29305691
171 results