131 related articles for article (PubMed ID: 32670189)
21. Treatment in myotonia and periodic paralysis.
Meola G; Sansone V
Rev Neurol (Paris); 2004 May; 160(5 Pt 2):S55-69. PubMed ID: 15269662
[TBL] [Abstract][Full Text] [Related]
22. Therapy in myotonic disorders and in muscle channelopathies.
Meola G; Sansone V
Neurol Sci; 2000; 21(5 Suppl):S953-61. PubMed ID: 11382195
[TBL] [Abstract][Full Text] [Related]
23. Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians.
Dupré N; Chrestian N; Bouchard JP; Rossignol E; Brunet D; Sternberg D; Brais B; Mathieu J; Puymirat J
Neuromuscul Disord; 2009 May; 19(5):330-4. PubMed ID: 18337100
[TBL] [Abstract][Full Text] [Related]
24. Multiple sclerosis and non-dystrophic myotonias: do they share a common pathophysiology?
Portaro S; Naro A; Russo M; Bramanti P; Lauria P; D'Aleo G; La Rosa G; Bramanti A; Calabrò RS
Funct Neurol; 2018; 33(4):194-199. PubMed ID: 30663965
[TBL] [Abstract][Full Text] [Related]
25. In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotonia.
Trip J; Drost G; Verbove DJ; van der Kooi AJ; Kuks JB; Notermans NC; Verschuuren JJ; de Visser M; van Engelen BG; Faber CG; Ginjaar IB
Eur J Hum Genet; 2008 Aug; 16(8):921-9. PubMed ID: 18337730
[TBL] [Abstract][Full Text] [Related]
26. Identification of novel mutations of the CLCN1 gene for myotonia congenital in China.
Meng YX; Zhao Z; Shen HR; Bing Q; Hu J
Neurol Res; 2016 Jan; 38(1):40-4. PubMed ID: 27118449
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. N1366S mutation of human skeletal muscle sodium channel causes paramyotonia congenita.
Ke Q; Ye J; Tang S; Wang J; Luo B; Ji F; Zhang X; Yu Y; Cheng X; Li Y
J Physiol; 2017 Nov; 595(22):6837-6850. PubMed ID: 28940424
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 gene.
Nagamitsu S; Matsuura T; Khajavi M; Armstrong R; Gooch C; Harati Y; Ashizawa T
Neurology; 2000 Dec; 55(11):1697-703. PubMed ID: 11113225
[TBL] [Abstract][Full Text] [Related]
31. Imaging alterations in skeletal muscle channelopathies: a study in 15 patients.
Maggi L; Brugnoni R; Canioni E; Maccagnano E; Bernasconi P; Morandi L
Acta Myol; 2015 Dec; 34(2-3):109-15. PubMed ID: 27199537
[TBL] [Abstract][Full Text] [Related]
32. Phenotypic variability and molecular genetics in proximal myotonic myopathy.
Papadimas GK; Kekou K; Papadopoulos C; Kararizou E; Kanavakis E; Manta P
Muscle Nerve; 2015 May; 51(5):686-91. PubMed ID: 25186227
[TBL] [Abstract][Full Text] [Related]
33. Transient muscular weakness in severe recessive myotonia congenita. Improvement of isometric muscle force by drugs relieving myotomic stiffness.
Ricker K; Haass A; Hertel G; Mertens HG
J Neurol; 1978 Aug; 218(4):253-62. PubMed ID: 81274
[TBL] [Abstract][Full Text] [Related]
34. Mouse models of non-dystrophic and dystrophic myotonia exhibit nociplastic pain-like behaviors.
Nelson TS; Duran P; Calderon-Rivera A; Gomez K; Loya-Lopez S; Khanna R
bioRxiv; 2024 Jun; ():. PubMed ID: 38948724
[TBL] [Abstract][Full Text] [Related]
35. Use of Clinical and Electrical Myotonia to Differentiate Childhood Myopathies.
Ghosh PS; Sorenson EJ
J Child Neurol; 2015 Sep; 30(10):1300-6. PubMed ID: 25637645
[TBL] [Abstract][Full Text] [Related]
36. Phenotypic variability in childhood of skeletal muscle sodium channelopathies.
Yoshinaga H; Sakoda S; Shibata T; Akiyama T; Oka M; Yuan JH; Takashima H; Takahashi MP; Kitamura T; Murakami N; Kobayashi K
Pediatr Neurol; 2015 May; 52(5):504-8. PubMed ID: 25724373
[TBL] [Abstract][Full Text] [Related]
37. Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene.
Morales F; Cuenca P; del Valle G; Vásquez M; Brian R; Sittenfeld M; Johnson K; Lin X; Ashizawa T
Rev Biol Trop; 2008 Mar; 56(1):1-11. PubMed ID: 18624224
[TBL] [Abstract][Full Text] [Related]
38. Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in
Maggi L; Brugnoni R; Canioni E; Tonin P; Saletti V; Sola P; Piccinelli SC; Colleoni L; Ferrigno P; Pini A; Masson R; Manganelli F; Lietti D; Vercelli L; Ricci G; Bruno C; Tasca G; Pizzuti A; Padovani A; Fusco C; Pegoraro E; Ruggiero L; Ravaglia S; Siciliano G; Morandi L; Dubbioso R; Mongini T; Filosto M; Tramacere I; Mantegazza R; Bernasconi P
Front Neurol; 2020; 11():646. PubMed ID: 32849172
[No Abstract] [Full Text] [Related]
39. Myotonia congenita: mutation spectrum of
Milla CP; De Castro CP; Gómez-González C; Martínez-Montero P; Pascual Pascual SI; Molano Mateos J
J Genet; 2019 Sep; 98():. PubMed ID: 31544778
[TBL] [Abstract][Full Text] [Related]
40. Influences of Pregnancy on Different Genetic Subtypes of Non-Dystrophic Myotonia and Periodic Paralysis.
Rudnik-Schöneborn S; Witsch-Baumgartner M; Zerres K
Gynecol Obstet Invest; 2016; 81(5):472-6. PubMed ID: 27300293
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
