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24. Andersen-Tawil Syndrome: A Comprehensive Review. Pérez-Riera AR; Barbosa-Barros R; Samesina N; Pastore CA; Scanavacca M; Daminello-Raimundo R; de Abreu LC; Nikus K; Brugada P Cardiol Rev; 2021 Jul-Aug 01; 29(4):165-177. PubMed ID: 32947483 [TBL] [Abstract][Full Text] [Related]
25. Marked reduction in paralytic attacks in a patient with Andersen-Tawil syndrome switched from acetazolamide to dichlorphenamide. Gupta A; Iyadurai S; Roggenbuck J; LoRusso S Neuromuscul Disord; 2021 Jul; 31(7):656-659. PubMed ID: 34078557 [TBL] [Abstract][Full Text] [Related]
26. Electrophysiological mechanisms of ventricular arrhythmias in relation to Andersen-Tawil syndrome under conditions of reduced IK1: a simulation study. Sung RJ; Wu SN; Wu JS; Chang HD; Luo CH Am J Physiol Heart Circ Physiol; 2006 Dec; 291(6):H2597-605. PubMed ID: 16877549 [TBL] [Abstract][Full Text] [Related]
27. Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation. Delannoy E; Sacher F; Maury P; Mabo P; Mansourati J; Magnin I; Camous JP; Tournant G; Rendu E; Kyndt F; Haïssaguerre M; Bézieau S; Guyomarch B; Le Marec H; Fressart V; Denjoy I; Probst V Europace; 2013 Dec; 15(12):1805-11. PubMed ID: 23867365 [TBL] [Abstract][Full Text] [Related]
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30. Novel de novo mutation in the KCNJ2 gene in a patient with Andersen-Tawil syndrome. Kim JB; Chung KW Pediatr Neurol; 2009 Dec; 41(6):464-6. PubMed ID: 19931173 [TBL] [Abstract][Full Text] [Related]
31. Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome? van der Werf-'t Lam AS; van Haeringen A; Rinnen T; Robles de Medina RM; Wilde AAM; Hennekam RC; Barge-Schaapveld DQCM Eur J Med Genet; 2022 Jan; 65(1):104382. PubMed ID: 34748995 [TBL] [Abstract][Full Text] [Related]
32. Andersen-Tawil syndrome: definition of a neurocognitive phenotype. Yoon G; Quitania L; Kramer JH; Fu YH; Miller BL; Ptácek LJ Neurology; 2006 Jun; 66(11):1703-10. PubMed ID: 16769944 [TBL] [Abstract][Full Text] [Related]
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39. Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome. Ördög B; Hategan L; Kovács M; Seprényi G; Kohajda Z; Nagy I; Hegedűs Z; Környei L; Jost N; Katona M; Szekeres M; Forster T; Papp JG; Varró A; Sepp R Can J Physiol Pharmacol; 2015 Jul; 93(7):569-75. PubMed ID: 26103554 [TBL] [Abstract][Full Text] [Related]
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