PubMed (Bookshelf cited) for id: 318633

Year	Number of Results
1991	1
1993	2
1994	1
1996	1
1999	2
2001	1
2002	2
2003	3
2004	4
2005	5
2006	3
2007	4
2008	2
2009	3
2010	4
2012	5
2013	6
2014	16
2015	12
2016	9
2017	8
2018	1
2024	0

1

A Distinct Phenotype in a Novel ATP1A3 Mutation: Connecting the Two Ends of a Spectrum.

Pereira P, Guerreiro A, Fonseca M, Halpern C, Pinto-Basto J, Monteiro JP. Pereira P, et al. Mov Disord Clin Pract. 2015 Nov 28;3(4):398-401. doi: 10.1002/mdc3.12263. eCollection 2016 Jul-Aug. Mov Disord Clin Pract. 2015. PMID: 30713930 Free PMC article. No abstract available.

2

Failure of Pallidal Deep Brain Stimulation in a Case of Rapid-Onset Dystonia Parkinsonism (DYT12).

Brücke C, Horn A, Huppke P, Kupsch A, Schneider GH, Kühn AA. Brücke C, et al. Mov Disord Clin Pract. 2014 Dec 30;2(1):76-78. doi: 10.1002/mdc3.12124. eCollection 2015 Mar. Mov Disord Clin Pract. 2014. PMID: 30713884 Free PMC article. No abstract available.

3

Beyond Dystonia-Parkinsonism: Chorea and Ataxia with ATP1A3 Mutations.

de Gusmao CM, Dy M, Sharma N. de Gusmao CM, et al. Mov Disord Clin Pract. 2016 Jan 29;3(4):402-404. doi: 10.1002/mdc3.12317. eCollection 2016 Jul-Aug. Mov Disord Clin Pract. 2016. PMID: 30363590 Free PMC article.

4

Novel pregnancy-triggered episodes of CAPOS syndrome.

Chang IJ, Adam MP, Jayadev S, Bird TD, Natarajan N, Glass IA. Chang IJ, et al. Am J Med Genet A. 2018 Jan;176(1):235-240. doi: 10.1002/ajmg.a.38502. Epub 2017 Nov 1. Am J Med Genet A. 2018. PMID: 29090527 Free PMC article. Review.

5

Fever-Induced Paroxysmal Weakness and Encephalopathy, a New Phenotype of ATP1A3 Mutation.

Yano ST, Silver K, Young R, DeBrosse SD, Ebel RS, Swoboda KJ, Acsadi G. Yano ST, et al. Pediatr Neurol. 2017 Aug;73:101-105. doi: 10.1016/j.pediatrneurol.2017.04.022. Epub 2017 Apr 29. Pediatr Neurol. 2017. PMID: 28647130

6

Early Diagnosis of CAPOS Syndrome Before Acute-Onset Ataxia-Review of the Literature and a New Family.

Duat Rodriguez A, Prochazkova M, Santos Santos S, Rubio Cabezas O, Cantarin Extremera V, Gonzalez-Gutierrez-Solana L. Duat Rodriguez A, et al. Pediatr Neurol. 2017 Jun;71:60-64. doi: 10.1016/j.pediatrneurol.2017.01.009. Epub 2017 Jan 25. Pediatr Neurol. 2017. PMID: 28483396 Review.

7

Familial childhood-onset progressive cerebellar syndrome associated with the ATP1A3 mutation.

Jaffer F, Fawcett K, Sims D, Heger A, Houlden H, Hanna MG, Kingston H, Sisodiya SM. Jaffer F, et al. Neurol Genet. 2017 Mar 27;3(2):e145. doi: 10.1212/NXG.0000000000000145. eCollection 2017 Apr. Neurol Genet. 2017. PMID: 28382329 Free PMC article. No abstract available.

8

Research conference summary from the 2014 International Task Force on ATP1A3-Related Disorders.

Rosewich H, Sweney MT, DeBrosse S, Ess K, Ozelius L, Andermann E, Andermann F, Andrasco G, Belgrade A, Brashear A, Ciccodicola S, Egan L, George AL Jr, Lewelt A, Magelby J, Merida M, Newcomb T, Platt V, Poncelin D, Reyna S, Sasaki M, Sotero de Menezes M, Sweadner K, Viollet L, Zupanc M, Silver K, Swoboda K. Rosewich H, et al. Neurol Genet. 2017 Mar 2;3(2):e139. doi: 10.1212/NXG.0000000000000139. eCollection 2017 Apr. Neurol Genet. 2017. PMID: 28293679 Free PMC article.

9

Alternating Hemiplegia of Childhood: Pharmacological treatment of 30 Italian patients.

Pisciotta L, Gherzi M, Stagnaro M, Calevo MG, Giannotta M, Vavassori MR, Veneselli E; I.B.AHC Consortium; De Grandis E. Pisciotta L, et al. Brain Dev. 2017 Jun;39(6):521-528. doi: 10.1016/j.braindev.2017.02.001. Epub 2017 Feb 27. Brain Dev. 2017. PMID: 28249736

10

Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases.

Westenberger A, Max C, Brüggemann N, Domingo A, Grütz K, Pawlack H, Weissbach A, Kühn AA, Spiegler J, Lang AE, Sperner J, Fung VSC, Schallner J, Gillessen-Kaesbach G, Münchau A, Klein C. Westenberger A, et al. J Pediatr. 2017 Feb;181:306-308.e1. doi: 10.1016/j.jpeds.2016.10.079. Epub 2016 Dec 6. J Pediatr. 2017. PMID: 27931826

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