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47. A skeletal muscle sodium channel mutation in a Japanese family with paramyotonia congenita. Yamada T; Ochi H; Hara H; Yoshimura T; Kobayashi T J Neurol Sci; 1995 Nov; 133(1-2):192-3. PubMed ID: 8583225 [No Abstract] [Full Text] [Related]
48. Myotonia congenita with painful muscle cramps. Sunohara N; Tomi H; Nakamura A; Arahata K; Nonaka I Intern Med; 1996 Jun; 35(6):507-11. PubMed ID: 8835606 [TBL] [Abstract][Full Text] [Related]
49. Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita. McClatchey AI; Van den Bergh P; Pericak-Vance MA; Raskind W; Verellen C; McKenna-Yasek D; Rao K; Haines JL; Bird T; Brown RH Cell; 1992 Feb; 68(4):769-74. PubMed ID: 1310898 [TBL] [Abstract][Full Text] [Related]
50. [A case of paramyotonia congenita]. Arai J; Miyake S; Hayashi M; Iwamoto H; Misugi N No To Hattatsu; 1985 Nov; 17(6):583-7. PubMed ID: 4084423 [No Abstract] [Full Text] [Related]
51. [Electromyographic study of 2 cases of von Eulenburg's paramyotonia congenita]. Isch F; Isch-Treussard C; Jésel M; Warter JM Rev Neurol (Paris); 1968 Jun; 118(6):536-42. PubMed ID: 5724664 [No Abstract] [Full Text] [Related]
52. Myotonia Congenita (Thomsen's disease). Kim C; Yamada S Hawaii Med J; 1974 Jan; 33(1):15-8. PubMed ID: 4811601 [No Abstract] [Full Text] [Related]
53. Treatment of paramyotonia congenita with acetazolamide. Benstead TJ; Camfield PR; King DB Can J Neurol Sci; 1987 May; 14(2):156-8. PubMed ID: 3607618 [TBL] [Abstract][Full Text] [Related]
54. Dosage effect of a dominant CLCN1 mutation: a novel syndrome. Bernard G; Poulin C; Puymirat J; Sternberg D; Shevell M J Child Neurol; 2008 Feb; 23(2):163-6. PubMed ID: 18263754 [TBL] [Abstract][Full Text] [Related]
55. Dystrophia myotonica and myotonia congenita concurring in one family. A clinical and genetic study. Höweler CJ; Busch HF; Bernini LF; van Loghem E; Meera Khan P; Nijenhuis LE Brain; 1980 Sep; 103(3):497-513. PubMed ID: 7417778 [TBL] [Abstract][Full Text] [Related]