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27. Paramyotonia congenita and hyperkalemic periodic paralysis associated with a Met 1592 Val substitution in the skeletal muscle sodium channel alpha subunit--a large kindred with a novel phenotype. Kelly P; Yang WS; Costigan D; Farrell MA; Murphy S; Hardiman O Neuromuscul Disord; 1997 Mar; 7(2):105-11. PubMed ID: 9131651 [TBL] [Abstract][Full Text] [Related]
28. A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene. Schoser BG; Schröder JM; Grimm T; Sternberg D; Kress W Muscle Nerve; 2007 May; 35(5):599-606. PubMed ID: 17212350 [TBL] [Abstract][Full Text] [Related]
29. A case of paramyotonia congenita in pregnancy. Brooks EK; Schweitzer D; Robinson HL Obstet Med; 2020 Dec; 13(4):192-194. PubMed ID: 33343696 [TBL] [Abstract][Full Text] [Related]
30. A case of paramyotonia congenita without periodic paralysis: electrophysiological and molecular genetic studies. Park JH; Lee YW; Park SA; Lee TK; Rho HJ; Sung KB Neurologist; 2010 May; 16(3):203-5. PubMed ID: 20445432 [TBL] [Abstract][Full Text] [Related]
31. [Periodic paramyotonic paralysis]. Badalian LO; Iadgarov IS; Temin PA; Arkhipov BA; Bulaeva NV Zh Nevropatol Psikhiatr Im S S Korsakova; 1988; 88(11):3-7. PubMed ID: 2975906 [TBL] [Abstract][Full Text] [Related]
32. Potassium uptake in muscle during paramyotonic weakness. Moxley RT; Ricker K; Kingston WJ; Böhlen R Neurology; 1989 Jul; 39(7):952-5. PubMed ID: 2500620 [TBL] [Abstract][Full Text] [Related]
33. Linkage of atypical myotonia congenita to a sodium channel locus. Ptacek LJ; Tawil R; Griggs RC; Storvick D; Leppert M Neurology; 1992 Feb; 42(2):431-3. PubMed ID: 1310531 [TBL] [Abstract][Full Text] [Related]
34. Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17. Koch MC; Ricker K; Otto M; Grimm T; Bender K; Zoll B; Harper PS; Lehmann-Horn F; Rüdel R; Hoffman EP Hum Genet; 1991 Nov; 88(1):71-4. PubMed ID: 1660029 [TBL] [Abstract][Full Text] [Related]
35. A novel N440K sodium channel mutation causes myotonia with exercise-induced weakness--exclusion of CLCN1 exon deletion/duplication by MLPA. Lehmann-Horn F; Orth M; Kuhn M; Jurkat-Rott K Acta Myol; 2011 Oct; 30(2):133-7. PubMed ID: 22106717 [TBL] [Abstract][Full Text] [Related]
36. [A family with heat-sensitive myotonia alternating with hypokalemic periodic paralysis]. Aoki T; Sugiura Y; Sugiyama Y; Ogata M; Hida C; Honma M; Yamamoto T Rinsho Shinkeigaku; 2000 Apr; 40(4):358-63. PubMed ID: 10967653 [TBL] [Abstract][Full Text] [Related]
37. Distinguishing paramyotonia congenita and myotonia congenita by electromyography. Subramony SH; Malhotra CP; Mishra SK Muscle Nerve; 1983 Jun; 6(5):374-9. PubMed ID: 6888415 [TBL] [Abstract][Full Text] [Related]
38. Myotonia not aggravated by cooling. Force and relaxation of the adductor pollicis in normal subjects and in myotonia as compared to paramyotonia. Ricker K; Hertel G; Langscheid K; Stodieck G J Neurol; 1977 Aug; 216(1):9-20. PubMed ID: 72799 [TBL] [Abstract][Full Text] [Related]