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

Year Number of Results
2004 1
2007 1
2009 1
2010 2
2011 2
2012 1
2013 2
2014 2
2015 2
2016 1
2017 1
2018 2
2019 1
2020 2
2021 3
2022 1
2023 0
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23 results
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Page 1
Neuronal mechanism of a BK channelopathy in absence epilepsy and dyskinesia.
Dong P, Zhang Y, Hunanyan AS, Mikati MA, Cui J, Yang H. Dong P, et al. Among authors: hunanyan as. Proc Natl Acad Sci U S A. 2022 Mar 22;119(12):e2200140119. doi: 10.1073/pnas.2200140119. Epub 2022 Mar 14. Proc Natl Acad Sci U S A. 2022. PMID: 35286197 Free PMC article.
Diagnosis and Treatment of Alternating Hemiplegia of Childhood.
Masoud M, Prange L, Wuchich J, Hunanyan A, Mikati MA. Masoud M, et al. Among authors: hunanyan a. Curr Treat Options Neurol. 2017 Feb;19(2):8. doi: 10.1007/s11940-017-0444-7. Curr Treat Options Neurol. 2017. PMID: 28337648 Review.
Alternating hemiplegia of childhood: evolution over time and mouse model corroboration.
Uchitel J, Wallace K, Tran L, Abrahamsen T, Hunanyan A, Prange L, Jasien J, Caligiuri L, Pratt M, Rikard B, Fons C, De Grandis E, Vezyroglou A, Heinzen EL, Goldstein DB, Vavassori R, Papadopoulou MT, Cocco I, Moré R; Duke AHC Research Group; French AHC Consortium; Arzimanoglou A, Panagiotakaki E, Mikati MA. Uchitel J, et al. Among authors: hunanyan a. Brain Commun. 2021 Jun 4;3(3):fcab128. doi: 10.1093/braincomms/fcab128. eCollection 2021. Brain Commun. 2021. PMID: 34396101 Free PMC article.
D-DEMØ, a distinct phenotype caused by ATP1A3 mutations.
Prange L, Pratt M, Herman K, Schiffmann R, Mueller DM, McLean M, Mendez MM, Walley N, Heinzen EL, Goldstein D, Shashi V, Hunanyan A, Pagadala V, Mikati MA. Prange L, et al. Among authors: hunanyan a. Neurol Genet. 2020 Aug 4;6(5):e466. doi: 10.1212/NXG.0000000000000466. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 32802951 Free PMC article.
The epileptology of alternating hemiplegia of childhood.
Uchitel J, Helseth A, Prange L, McLean M, Ghusayni R, Sachdev M, Hunanyan A, Mikati MA. Uchitel J, et al. Among authors: hunanyan a. Neurology. 2019 Sep 24;93(13):e1248-e1259. doi: 10.1212/WNL.0000000000008159. Epub 2019 Sep 4. Neurology. 2019. PMID: 31484714
Novel E815K knock-in mouse model of alternating hemiplegia of childhood.
Helseth AR, Hunanyan AS, Adil S, Linabarger M, Sachdev M, Abdelnour E, Arehart E, Szabo M, Richardson J, Wetsel WC, Hochgeschwender U, Mikati MA. Helseth AR, et al. Among authors: hunanyan as. Neurobiol Dis. 2018 Nov;119:100-112. doi: 10.1016/j.nbd.2018.07.028. Epub 2018 Jul 30. Neurobiol Dis. 2018. PMID: 30071271
Cardiac phenotype in ATP1A3-related syndromes: A multicenter cohort study.
Balestrini S, Mikati MA, Álvarez-García-Rovés R, Carboni M, Hunanyan AS, Kherallah B, McLean M, Prange L, De Grandis E, Gagliardi A, Pisciotta L, Stagnaro M, Veneselli E, Campistol J, Fons C, Pias-Peleteiro L, Brashear A, Miller C, Samões R, Brankovic V, Padiath QS, Potic A, Pilch J, Vezyroglou A, Bye AME, Davis AM, Ryan MM, Semsarian C, Hollingsworth G, Scheffer IE, Granata T, Nardocci N, Ragona F, Arzimanoglou A, Panagiotakaki E, Carrilho I, Zucca C, Novy J, Dzieżyc K, Parowicz M, Mazurkiewicz-Bełdzińska M, Weckhuysen S, Pons R, Groppa S, Sinden DS, Pitt GS, Tinker A, Ashworth M, Michalak Z, Thom M, Cross JH, Vavassori R, Kaski JP, Sisodiya SM. Balestrini S, et al. Among authors: hunanyan as. Neurology. 2020 Nov 24;95(21):e2866-e2879. doi: 10.1212/WNL.0000000000010794. Epub 2020 Sep 10. Neurology. 2020. PMID: 32913013 Free PMC article.
23 results