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

Year Number of Results
2017 2
2018 1
2019 4
2020 6
2021 4
2022 2
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18 results
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Page 1
Diagnosis and Treatment of Alternating Hemiplegia of Childhood.
Masoud M, Prange L, Wuchich J, Hunanyan A, Mikati MA. Masoud M, et al. Among authors: prange l. Curr Treat Options Neurol. 2017 Feb;19(2):8. doi: 10.1007/s11940-017-0444-7. Curr Treat Options Neurol. 2017. PMID: 28337648 Review.
Social impairments in alternating hemiplegia of childhood.
Uchitel J, Abdelnour E, Boggs A, Prange L, Pratt M, Bonner M, Jasien J, Dawson G, Abrahamsen T, Mikati MA. Uchitel J, et al. Among authors: prange l. Dev Med Child Neurol. 2020 Jul;62(7):820-826. doi: 10.1111/dmcn.14473. Epub 2020 Feb 7. Dev Med Child Neurol. 2020. PMID: 32031250 Free 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: prange l. Neurology. 2019 Sep 24;93(13):e1248-e1259. doi: 10.1212/WNL.0000000000008159. Epub 2019 Sep 4. Neurology. 2019. PMID: 31484714
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. Neurol Genet. 2020 Aug 4;6(5):e466. doi: 10.1212/NXG.0000000000000466. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 32802951 Free PMC article.
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: prange l. Brain Commun. 2021 Jun 4;3(3):fcab128. doi: 10.1093/braincomms/fcab128. eCollection 2021. Brain Commun. 2021. PMID: 34396101 Free PMC article.
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: prange l. Neurology. 2020 Nov 24;95(21):e2866-e2879. doi: 10.1212/WNL.0000000000010794. Epub 2020 Sep 10. Neurology. 2020. PMID: 32913013 Free PMC article.
ATP1A3-Encoded Sodium-Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by Bradycardia.
Moya-Mendez ME, Ogbonna C, Ezekian JE, Rosamilia MB, Prange L, de la Uz C, Kim JJ, Howard T, Garcia J, Nussbaum R, Truty R, Callis TE, Funk E, Heyes M, Dear GL, Carboni MP, Idriss SF, Mikati MA, Landstrom AP. Moya-Mendez ME, et al. Among authors: prange l. J Am Heart Assoc. 2021 Sep 7;10(17):e019887. doi: 10.1161/JAHA.120.019887. Epub 2021 Aug 28. J Am Heart Assoc. 2021. PMID: 34459253 Free PMC article.
18 results