636 related articles for article (PubMed ID: 26036855)
21. Sodium Channelopathies of Skeletal Muscle.
Cannon SC
Handb Exp Pharmacol; 2018; 246():309-330. PubMed ID: 28939973
[TBL] [Abstract][Full Text] [Related]
22. Clinical comparison and functional study of the L703P: a recurrent mutation in human SCN4A that causes sodium channel myotonia.
Ke Q; Zhao Y; Li Y; Ye J; Tang S; He F; Ji F; Dai X; Ni J; Li Y; Griggs RC; Cheng X
Neuromuscul Disord; 2022 Oct; 32(10):811-819. PubMed ID: 36050252
[TBL] [Abstract][Full Text] [Related]
23. Functional and Structural Characterization of ClC-1 and Na
Brenes O; Barbieri R; Vásquez M; Vindas-Smith R; Roig J; Romero A; Valle GD; Bermúdez-Guzmán L; Bertelli S; Pusch M; Morales F
Cells; 2021 Feb; 10(2):. PubMed ID: 33670307
[TBL] [Abstract][Full Text] [Related]
24. A SCN4A mutation causing paramyotonia congenita.
Palma C; Prior C; Gómez-González C; Rodríguez-Antolin C; Martínez-Montero P; Pérez de Ayala L; Pascual SI; Molano Mateos J
Neuromuscul Disord; 2017 Dec; 27(12):1123-1125. PubMed ID: 29111379
[TBL] [Abstract][Full Text] [Related]
25. "Status myotonicus" in Na
Rempe T; Subramony SH
Neuromuscul Disord; 2020 May; 30(5):424-426. PubMed ID: 32327288
[TBL] [Abstract][Full Text] [Related]
26. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.
Pambrun T; Mercier A; Chatelier A; Patri S; Schott JJ; Le Scouarnec S; Chahine M; Degand B; Bois P
Heart Rhythm; 2014 Aug; 11(8):1393-400. PubMed ID: 24768612
[TBL] [Abstract][Full Text] [Related]
27. Changes of Resurgent Na
Huang CW; Lai HJ; Lin PC; Lee MJ
Int J Mol Sci; 2020 Apr; 21(7):. PubMed ID: 32276507
[TBL] [Abstract][Full Text] [Related]
28. [Clinical and molecular genetic analysis of a family with normokalemic periodic paralysis].
Wei CJ; Wang D; Wang S; Jiao H; Hong DJ; Pu LH; Xiong H
Zhonghua Er Ke Za Zhi; 2013 Jan; 51(1):47-51. PubMed ID: 23527931
[TBL] [Abstract][Full Text] [Related]
29. Myotonic discharges discriminate chloride from sodium muscle channelopathies.
Drost G; Stunnenberg BC; Trip J; Borm G; McGill KC; Ginjaar IH; van der Kooi AW; Zwarts MJ; van Engelen BG; Faber CG; Stegeman DF; Lateva Z
Neuromuscul Disord; 2015 Jan; 25(1):73-80. PubMed ID: 25454733
[TBL] [Abstract][Full Text] [Related]
30. Non-dystrophic myotonia: prospective study of objective and patient reported outcomes.
Trivedi JR; Bundy B; Statland J; Salajegheh M; Rayan DR; Venance SL; Wang Y; Fialho D; Matthews E; Cleland J; Gorham N; Herbelin L; Cannon S; Amato A; Griggs RC; Hanna MG; Barohn RJ;
Brain; 2013 Jul; 136(Pt 7):2189-200. PubMed ID: 23771340
[TBL] [Abstract][Full Text] [Related]
31. Pathological findings in a patient with non-dystrophic myotonia with a mutation of the SCN4A gene; a case report.
Hata T; Nagasaka T; Koh K; Tsuchiya M; Ichinose Y; Nan H; Shindo K; Takiyama Y
BMC Neurol; 2019 Jun; 19(1):125. PubMed ID: 31189464
[TBL] [Abstract][Full Text] [Related]
32. Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients.
Brugnoni R; Maggi L; Canioni E; Verde F; Gallone A; Ariatti A; Filosto M; Petrelli C; Logullo FO; Esposito M; Ruggiero L; Tonin P; Riguzzi P; Pegoraro E; Torri F; Ricci G; Siciliano G; Silani V; Merlini L; De Pasqua S; Liguori R; Pini A; Mariotti C; Moroni I; Imbrici P; Desaphy JF; Mantegazza R; Bernasconi P
Neuromuscul Disord; 2021 Apr; 31(4):336-347. PubMed ID: 33573884
[TBL] [Abstract][Full Text] [Related]
33. New phenotype and neonatal onset of sodium channel myotonia in a child with a novel mutation of SCN4A gene.
Fusco C; Frattini D; Salerno GG; Canali E; Bernasconi P; Maggi L
Brain Dev; 2015 Oct; 37(9):891-3. PubMed ID: 25735906
[TBL] [Abstract][Full Text] [Related]
34. A Novel De Novo Heterozygous SCN4a Mutation Causing Congenital Myopathy, Myotonia and Multiple Congenital Anomalies.
Waldrop M; Amornvit J; Pierson CR; Boue DR; Sahenk Z
J Neuromuscul Dis; 2019; 6(4):467-473. PubMed ID: 31609695
[TBL] [Abstract][Full Text] [Related]
35. Flecainide-Induced Brugada Syndrome in a Patient With Skeletal Muscle Sodium Channelopathy: A Case Report With Critical Therapeutical Implications and Review of the Literature.
Cavalli M; Fossati B; Vitale R; Brigonzi E; Ricigliano VAG; Saraceno L; Cardani R; Pappone C; Meola G
Front Neurol; 2018; 9():385. PubMed ID: 29899727
[TBL] [Abstract][Full Text] [Related]
36. Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy.
Zaharieva IT; Thor MG; Oates EC; van Karnebeek C; Hendson G; Blom E; Witting N; Rasmussen M; Gabbett MT; Ravenscroft G; Sframeli M; Suetterlin K; Sarkozy A; D'Argenzio L; Hartley L; Matthews E; Pitt M; Vissing J; Ballegaard M; Krarup C; Slørdahl A; Halvorsen H; Ye XC; Zhang LH; Løkken N; Werlauff U; Abdelsayed M; Davis MR; Feng L; Phadke R; Sewry CA; Morgan JE; Laing NG; Vallance H; Ruben P; Hanna MG; Lewis S; Kamsteeg EJ; Männikkö R; Muntoni F
Brain; 2016 Mar; 139(Pt 3):674-91. PubMed ID: 26700687
[TBL] [Abstract][Full Text] [Related]
37. SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype.
Bugiardini E; Rivolta I; Binda A; Soriano Caminero A; Cirillo F; Cinti A; Giovannoni R; Botta A; Cardani R; Wicklund MP; Meola G
Neuromuscul Disord; 2015 Apr; 25(4):301-7. PubMed ID: 25660391
[TBL] [Abstract][Full Text] [Related]
38. Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.
Wahbi K; Algalarrondo V; Bécane HM; Fressart V; Beldjord C; Azibi K; Lazarus A; Berber N; Radvanyi-Hoffman H; Stojkovic T; Béhin A; Laforêt P; Eymard B; Hatem S; Duboc D
Arch Cardiovasc Dis; 2013 Dec; 106(12):635-43. PubMed ID: 24140416
[TBL] [Abstract][Full Text] [Related]
39. Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation.
Zhao C; Tang D; Huang H; Tang H; Yang Y; Yang M; Luo Y; Tao H; Tang J; Zhou X; Shi X
PLoS One; 2020; 15(5):e0233017. PubMed ID: 32407401
[TBL] [Abstract][Full Text] [Related]
40. A C-terminal skeletal muscle sodium channel mutation associated with myotonia disrupts fast inactivation.
Wu FF; Gordon E; Hoffman EP; Cannon SC
J Physiol; 2005 Jun; 565(Pt 2):371-80. PubMed ID: 15774523
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
