210 related articles for article (PubMed ID: 34789444)
1. Progression of alternating hemiplegia of childhood-related focal epilepsy to electrical status epilepticus in sleep with reversible encephalopathy.
Neupert D; Abbassi P; Prange L; Flamini R; Mikati MA
Epileptic Disord; 2022 Feb; 24(1):183-190. PubMed ID: 34789444
[TBL] [Abstract][Full Text] [Related]
2. Epileptic encephalopathy with features of rapid-onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation.
Tran L; Richards J; McDonald M; McConkie-Rosell A; Stong N; Jasien J; Shashi V; Mikati MA
Epileptic Disord; 2020 Feb; 22(1):103-109. PubMed ID: 32043468
[TBL] [Abstract][Full Text] [Related]
3. The epileptology of alternating hemiplegia of childhood.
Uchitel J; Helseth A; Prange L; McLean M; Ghusayni R; Sachdev M; Hunanyan A; Mikati MA
Neurology; 2019 Sep; 93(13):e1248-e1259. PubMed ID: 31484714
[TBL] [Abstract][Full Text] [Related]
4. Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations.
Marzin P; Mignot C; Dorison N; Dufour L; Ville D; Kaminska A; Panagiotakaki E; Dienpendaele AS; Penniello MJ; Nougues MC; Keren B; Depienne C; Nava C; Milh M; Villard L; Richelme C; Rivier C; Whalen S; Heron D; Lesca G; Doummar D
Brain Dev; 2018 Oct; 40(9):768-774. PubMed ID: 29861155
[TBL] [Abstract][Full Text] [Related]
5. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.
Sweney MT; Newcomb TM; Swoboda KJ
Pediatr Neurol; 2015 Jan; 52(1):56-64. PubMed ID: 25447930
[TBL] [Abstract][Full Text] [Related]
6. ATP1A3-related epileptic encephalopathy responding to ketogenic diet.
Schirinzi T; Graziola F; Cusmai R; Fusco L; Nicita F; Elia M; Travaglini L; Bertini E; Curatolo P; Vigevano F; Capuano A
Brain Dev; 2018 May; 40(5):433-438. PubMed ID: 29395663
[TBL] [Abstract][Full Text] [Related]
7. Faulty cardiac repolarization reserve in alternating hemiplegia of childhood broadens the phenotype.
Jaffer F; Avbersek A; Vavassori R; Fons C; Campistol J; Stagnaro M; De Grandis E; Veneselli E; Rosewich H; Gianotta M; Zucca C; Ragona F; Granata T; Nardocci N; Mikati M; Helseth AR; Boelman C; Minassian BA; Johns S; Garry SI; Scheffer IE; Gourfinkel-An I; Carrilho I; Aylett SE; Parton M; Hanna MG; Houlden H; Neville B; Kurian MA; Novy J; Sander JW; Lambiase PD; Behr ER; Schyns T; Arzimanoglou A; Cross JH; Kaski JP; Sisodiya SM
Brain; 2015 Oct; 138(Pt 10):2859-74. PubMed ID: 26297560
[TBL] [Abstract][Full Text] [Related]
8. Alternating hemiplegia of childhood and a pathogenic variant of ATP1A3: a case report and pathophysiological considerations.
Pavlidis E; Uldall P; Gøbel Madsen C; Nikanorova M; Fabricius M; Høgenhaven H; Pisani F; Møller RS; Gardella E; Rubboli G
Epileptic Disord; 2017 Jun; 19(2):226-230. PubMed ID: 28637637
[TBL] [Abstract][Full Text] [Related]
9. Alternating hemiplegia of childhood in Denmark: clinical manifestations and ATP1A3 mutation status.
Hoei-Hansen CE; Dali CÍ; Lyngbye TJ; Duno M; Uldall P
Eur J Paediatr Neurol; 2014 Jan; 18(1):50-4. PubMed ID: 24100174
[TBL] [Abstract][Full Text] [Related]
10. 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
Neurobiol Dis; 2018 Nov; 119():100-112. PubMed ID: 30071271
[TBL] [Abstract][Full Text] [Related]
11. Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2.
Pavone P; Pappalardo XG; Incorpora G; Falsaperla R; Marino SD; Corsello G; Parano E; Ruggieri M
Eur J Med Genet; 2020 Aug; 63(8):103957. PubMed ID: 32454213
[TBL] [Abstract][Full Text] [Related]
12. De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis.
Kanemasa H; Fukai R; Sakai Y; Torio M; Miyake N; Lee S; Ono H; Akamine S; Nishiyama K; Sanefuji M; Ishizaki Y; Torisu H; Saitsu H; Matsumoto N; Hara T
BMC Neurol; 2016 Sep; 16():174. PubMed ID: 27634470
[TBL] [Abstract][Full Text] [Related]
13. Alternating hemiplegia of childhood.
Ananthavarathan P; Kamourieh S
Handb Clin Neurol; 2023; 198():221-227. PubMed ID: 38043964
[TBL] [Abstract][Full Text] [Related]
14. 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;
Brain; 2021 Jun; 144(5):1435-1450. PubMed ID: 33880529
[TBL] [Abstract][Full Text] [Related]
15. [Genotype-phenotype correlation in patients with alternating hemiplegia of childhood].
Li SP; Zhang YH; Yang XL; Chen JY; Zeng Q; Zhang J; Wu XR
Zhonghua Er Ke Za Zhi; 2018 Nov; 56(11):811-817. PubMed ID: 30392204
[No Abstract] [Full Text] [Related]
16. ATP1A3 mutation in a Chinese girl with alternating hemiplegia of childhood--Potential target of treatment?
Wong VC; Kwong AK
Brain Dev; 2015 Oct; 37(9):907-10. PubMed ID: 25662428
[TBL] [Abstract][Full Text] [Related]
17. Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review.
Pavone P; Pappalardo XG; Ruggieri M; Falsaperla R; Parano E
Medicine (Baltimore); 2022 Aug; 101(31):e29413. PubMed ID: 35945798
[TBL] [Abstract][Full Text] [Related]
18. Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.
Viollet L; Glusman G; Murphy KJ; Newcomb TM; Reyna SP; Sweney M; Nelson B; Andermann F; Andermann E; Acsadi G; Barbano RL; Brown C; Brunkow ME; Chugani HT; Cheyette SR; Collins A; DeBrosse SD; Galas D; Friedman J; Hood L; Huff C; Jorde LB; King MD; LaSalle B; Leventer RJ; Lewelt AJ; Massart MB; Mérida MR; Ptáček LJ; Roach JC; Rust RS; Renault F; Sanger TD; Sotero de Menezes MA; Tennyson R; Uldall P; Zhang Y; Zupanc M; Xin W; Silver K; Swoboda KJ
PLoS One; 2015; 10(5):e0127045. PubMed ID: 25996915
[TBL] [Abstract][Full Text] [Related]
19. ATP1A3-related early childhood onset developmental and epileptic encephalopathy responding to corpus callosotomy: A case report.
Moriyama K; Mizuno T; Suzuki T; Inaji M; Maehara T; Fujita A; Kato M; Matsumoto N
Brain Dev; 2023 Jan; 45(1):77-81. PubMed ID: 36114075
[TBL] [Abstract][Full Text] [Related]
20. Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases.
Boonsimma P; Michael Gasser M; Netbaramee W; Wechapinan T; Srichomthong C; Ittiwut C; Wagner M; Krenn M; Zimprich F; Abicht A; Biskup S; Roser T; Borggraefe I; Suphapeetiporn K; Shotelersuk V
Gene; 2020 Jul; 749():144709. PubMed ID: 32339621
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]