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67. Transitional forms between myotonia congenita, dystrophia myotonica and paramyotonia congenita. Caughey JE N Z Med J; 1968 Mar; 67(429):347-50. PubMed ID: 5239622 [No Abstract] [Full Text] [Related]
69. Diffusely increased insertional activity: "EMG disease" or asymptomatic myotonia congenita? A report of 2 cases. Mitchell CW; Bertorini TE Arch Phys Med Rehabil; 2007 Sep; 88(9):1212-3. PubMed ID: 17826470 [TBL] [Abstract][Full Text] [Related]
70. [Hyperkalemic periodic paralysis: a Spanish family with the p.Thr704Met mutation in the SCN4A gene]. Narberhaus B; Cormand B; Cuenca-León E; Ribasés M; Monells J Neurologia; 2008 Sep; 23(7):427-35. PubMed ID: 18726720 [TBL] [Abstract][Full Text] [Related]
71. Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second gene. Wang J; Zhou J; Todorovic SM; Feero WG; Barany F; Conwit R; Hausmanowa-Petrusewicz I; Fidzianska A; Arahata K; Wessel HB Am J Hum Genet; 1993 Jun; 52(6):1074-84. PubMed ID: 8389097 [TBL] [Abstract][Full Text] [Related]
72. [Congenital paramyotonia: report of a clinicopathological and pedigree study]. Luo DR Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1987 Oct; 20(5):308-10. PubMed ID: 3450492 [No Abstract] [Full Text] [Related]
73. Hypokalemic paralysis in two patients with paramyotonia congenita (PC) and known hyperkalemic/exercise-induced weakness. Streib EW Muscle Nerve; 1989 Nov; 12(11):936-7. PubMed ID: 2608088 [TBL] [Abstract][Full Text] [Related]
74. [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]