PubMed (GeneRIF) for id: 477

Year	Number of Results
2001	1
2002	1
2003	6
2004	10
2005	6
2006	6
2007	9
2008	13
2009	9
2010	6
2011	5
2012	6
2013	10
2014	8
2015	3
2016	2
2017	1
2018	3
2019	2
2020	3
2021	6
2022	1
2023	1
2024	0

1

The clinical spectrum associated with ATP1A2 variants in Chinese pediatric patients.

Dai L, Ding C, Tian X, Liu M, Ma Y, Chen C, Ren X, Li H. Dai L, et al. Brain Dev. 2023 Sep;45(8):422-431. doi: 10.1016/j.braindev.2023.04.003. Epub 2023 May 2. Brain Dev. 2023. PMID: 37142513

2

Hemiplegic migraine type 2 with new mutation of the ATP1A2 gene in Japanese cases.

Oda I, Danno D, Saigoh K, Wolf J, Kawashita N, Hirano M, Samukawa M, Kitamura S, Kikui S, Takeshima T, Mitsui Y, Kusunoki S, Nagai Y. Oda I, et al. Neurosci Res. 2022 Jul;180:83-89. doi: 10.1016/j.neures.2022.03.002. Epub 2022 Mar 4. Neurosci Res. 2022. PMID: 35257835

3

Functional correlation of ATP1A2 mutations with phenotypic spectrum: from pure hemiplegic migraine to its variant forms.

Li Y, Tang W, Kang L, Kong S, Dong Z, Zhao D, Liu R, Yu S. Li Y, et al. J Headache Pain. 2021 Aug 12;22(1):92. doi: 10.1186/s10194-021-01309-4. J Headache Pain. 2021. PMID: 34384358 Free PMC article.

4

Hemiplegic migraine type 2 caused by a novel variant within the P-type ATPase motif in ATP1A2 concomitant with a CACNA1A variant.

Kubota T, Nabatame S, Sato R, Hama M, Nishiike U, Mochizuki H, Takahashi MP, Takeshima T. Kubota T, et al. Brain Dev. 2021 Oct;43(9):952-957. doi: 10.1016/j.braindev.2021.05.011. Epub 2021 Jun 3. Brain Dev. 2021. PMID: 34092402

5

ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria.

Vetro A, Nielsen HN, Holm R, Hevner RF, Parrini E, Powis Z, Møller RS, Bellan C, Simonati A, Lesca G, Helbig KL, Palmer EE, Mei D, Ballardini E, Van Haeringen A, Syrbe S, Leuzzi V, Cioni G, Curry CJ, Costain G, Santucci M, Chong K, Mancini GMS, Clayton-Smith J, Bigoni S, Scheffer IE, Dobyns WB, Vilsen B, Guerrini R; ATP1A2/A3-collaborators. Vetro A, et al. Brain. 2021 Jun 22;144(5):1435-1450. doi: 10.1093/brain/awab052. Brain. 2021. PMID: 33880529

6

Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2.

Antonaci F, Ravaglia S, Grieco GS, Gagliardi S, Cereda C, Costa A. Antonaci F, et al. J Headache Pain. 2021 Mar 12;22(1):12. doi: 10.1186/s10194-021-01221-x. J Headache Pain. 2021. PMID: 33711927 Free PMC article.

7

A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients.

Calame DG, Houck K, Lotze T, Emrick L, Parnes M. Calame DG, et al. Eur J Paediatr Neurol. 2021 Mar;31:21-26. doi: 10.1016/j.ejpn.2021.01.004. Epub 2021 Jan 16. Eur J Paediatr Neurol. 2021. PMID: 33578253

8

Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations.

Moya-Mendez ME, Mueller DM, Pratt M, Bonner M, Elliott C, Hunanyan A, Kucera G, Bock C, Prange L, Jasien J, Keough K, Shashi V, McDonald M, Mikati MA. Moya-Mendez ME, et al. Epilepsy Behav. 2021 Mar;116:107732. doi: 10.1016/j.yebeh.2020.107732. Epub 2021 Jan 23. Epilepsy Behav. 2021. PMID: 33493807 Free PMC article.

9

Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2.

Tang C, Unekawa M, Shibata M, Tomita Y, Izawa Y, Sugimoto H, Ikeda K, Kawakami K, Suzuki N, Nakahara J. Tang C, et al. Cephalalgia. 2020 Oct;40(11):1177-1190. doi: 10.1177/0333102420929028. Epub 2020 Jun 2. Cephalalgia. 2020. PMID: 32484063

10

Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine.

Rasmussen AH, Olofsson I, Chalmer MA, Olesen J, Hansen TF. Rasmussen AH, et al. J Med Genet. 2020 Sep;57(9):610-616. doi: 10.1136/jmedgenet-2019-106640. Epub 2020 Jan 24. J Med Genet. 2020. PMID: 31980564 Free PMC article.

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