454 related articles for article (PubMed ID: 1686388)
21. 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]
22. Lack of cold sensitivity in hyperkalemic periodic paralysis.
Subramony SH; Wee AS; Mishra SK
Muscle Nerve; 1986 Oct; 9(8):700-3. PubMed ID: 3785280
[TBL] [Abstract][Full Text] [Related]
23. A novel muscle sodium channel mutation causes painful congenital myotonia.
Rosenfeld J; Sloan-Brown K; George AL
Ann Neurol; 1997 Nov; 42(5):811-4. PubMed ID: 9392583
[TBL] [Abstract][Full Text] [Related]
24. Primary periodic paralyses.
Finsterer J
Acta Neurol Scand; 2008 Mar; 117(3):145-58. PubMed ID: 18031562
[TBL] [Abstract][Full Text] [Related]
25. A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification.
Ferriby D; Stojkovic T; Sternberg D; Hurtevent JF; Hurtevent JP; Vermersch P
Neuromuscul Disord; 2006 May; 16(5):321-4. PubMed ID: 16624558
[TBL] [Abstract][Full Text] [Related]
26. The myotonias: their diagnosis and treatment.
Moxley RT
Compr Ther; 1996 Jan; 22(1):8-21. PubMed ID: 8654027
[No Abstract] [Full Text] [Related]
27. Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.
Ptacek LJ; Tyler F; Trimmer JS; Agnew WS; Leppert M
Am J Hum Genet; 1991 Aug; 49(2):378-82. PubMed ID: 1651050
[TBL] [Abstract][Full Text] [Related]
28. [Molecular genetics of sodium channel myopathies].
Ruscák J
Bratisl Lek Listy; 1997 Dec; 98(12):701-7. PubMed ID: 9525070
[TBL] [Abstract][Full Text] [Related]
29. Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) family.
Sansone V; Rotondo G; Ptacek LJ; Meola G
Ital J Neurol Sci; 1994 Dec; 15(9):473-80. PubMed ID: 7721550
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Human disease hyperkalemic periodic paralysis is due to mutation in sodium channel alpha-subunit gene.
Kumar S
Indian J Exp Biol; 1991 May; 29(5):499. PubMed ID: 1655643
[No Abstract] [Full Text] [Related]
32. Hyperkalemic periodic paralysis associated with thyrotoxicosis.
Ahlawat SK; Gupta S
J Assoc Physicians India; 1993 Nov; 41(11):763-5. PubMed ID: 8005951
[No Abstract] [Full Text] [Related]
33. [Congenital paramyotonia, adynamia episodica hereditaria, or familial periodic paralysis with paramyotonia and hyperkalemia (author's transl)].
Serratrice G; Desnuelle C
Sem Hop; 1982 Apr; 58(14):841-8. PubMed ID: 6281896
[TBL] [Abstract][Full Text] [Related]
34. Normokalemic periodic paralysis revisited: does it exist?
Chinnery PF; Walls TJ; Hanna MG; Bates D; Fawcett PR
Ann Neurol; 2002 Aug; 52(2):251-2. PubMed ID: 12210802
[TBL] [Abstract][Full Text] [Related]
35. Paralysis periodica paramyotonica caused by SCN4A Arg1448Cys mutation.
Hsu WC; Huang YC; Wang CW; Hsueh CH; Lai LP; Yeh JH
J Formos Med Assoc; 2006 Jun; 105(6):503-7. PubMed ID: 16801039
[TBL] [Abstract][Full Text] [Related]
36. Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica.
Kim J; Hahn Y; Sohn EH; Lee YJ; Yun JH; Kim JM; Chung JH
J Neurol Neurosurg Psychiatry; 2001 May; 70(5):618-23. PubMed ID: 11309455
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Periodic paralysis, myotonia congenita and sarcolemmal ion channels: a success of the candidate gene approach.
Fontaine B
Neuromuscul Disord; 1993 Mar; 3(2):101-7. PubMed ID: 7689379
[TBL] [Abstract][Full Text] [Related]
39. Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family.
de Silva SM; Kuncl RW; Griffin JW; Cornblath DR; Chavoustie S
Muscle Nerve; 1990 Jan; 13(1):21-6. PubMed ID: 2325698
[TBL] [Abstract][Full Text] [Related]
40. Genetic approaches to the nosology of muscular disease: myotonias and similar diseases.
Becker PE
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):52-62. PubMed ID: 5293617
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
