197 related articles for article (PubMed ID: 1822800)
21. Progressive myopathy in hyperkalemic periodic paralysis.
Bradley WG; Taylor R; Rice DR; Hausmanowa-Petruzewicz I; Adelman LS; Jenkison M; Jedrzejowska H; Drac H; Pendlebury WW
Arch Neurol; 1990 Sep; 47(9):1013-7. PubMed ID: 2396930
[TBL] [Abstract][Full Text] [Related]
22. Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysis.
Lehmann-Horn F; Iaizzo PA; Hatt H; Franke C
Pflugers Arch; 1991 Apr; 418(3):297-9. PubMed ID: 1649995
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. A proposed mutation, Val781Ile, associated with hyperkalemic periodic paralysis and cardiac dysrhythmia is a benign polymorphism.
Green DS; Hayward LJ; George AL; Cannon SC
Ann Neurol; 1997 Aug; 42(2):253-6. PubMed ID: 9266738
[TBL] [Abstract][Full Text] [Related]
25. [Current status of clinical and molecular-biological research on familial periodic paralysis].
Shishiba Y
Nihon Rinsho; 1997 Dec; 55(12):3239-46. PubMed ID: 9436444
[TBL] [Abstract][Full Text] [Related]
26. Biphasic periodic paralysis.
Chesson AL; Schochet SS; Peters BH
Arch Neurol; 1979 Nov; 36(11):700-4. PubMed ID: 508128
[TBL] [Abstract][Full Text] [Related]
27. Identification of a Thr-to-Met mutation in the skeletal muscle sodium channel gene in hyperkalemic periodic paralysis of a Japanese family.
Arahata K; Wang J; Feero WG; Hayakawa H; Honda K; Sugita H; Hoffman EP
Ann N Y Acad Sci; 1993 Dec; 707():342-5. PubMed ID: 9137564
[No Abstract] [Full Text] [Related]
28. Hereditary nondystrophic myotonias and periodic paralyses.
Lehmann-Horn F; Rüdel R
Curr Opin Neurol; 1995 Oct; 8(5):402-10. PubMed ID: 8542048
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?
Baquero JL; Ayala RA; Wang J; Curless RG; Feero WG; Hoffman EP; Ebeid MR
Ann Neurol; 1995 Mar; 37(3):408-11. PubMed ID: 7695243
[TBL] [Abstract][Full Text] [Related]
31. Familial hyperkalemic periodic paralysis and bipolar disorder: a linkage and treatment study.
Pope HG; Hudson JI; Poskanzer DC; Yurgelun-Todd D
Biol Psychiatry; 1984 Oct; 19(10):1449-59. PubMed ID: 6440598
[TBL] [Abstract][Full Text] [Related]
32. Pathophysiologic and anesthetic considerations for patients with myotonia congenita or periodic paralyses.
Bandschapp O; Iaizzo PA
Paediatr Anaesth; 2013 Sep; 23(9):824-33. PubMed ID: 23802937
[TBL] [Abstract][Full Text] [Related]
33. Genotype-phenotype correlations in human skeletal muscle sodium channel diseases.
Rüdel R; Ricker K; Lehmann-Horn F
Arch Neurol; 1993 Nov; 50(11):1241-8. PubMed ID: 8215982
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Muscle channelopathies and electrophysiological approach.
Cherian A; Baheti NN; Kuruvilla A
Ann Indian Acad Neurol; 2008 Jan; 11(1):20-7. PubMed ID: 19966974
[TBL] [Abstract][Full Text] [Related]
36. [Recent findings on the genealogy, clinical aspects and histology of a family with periodic hyperkalemic paralysis].
Thomas C; Scwheitzer R; Isch F; Collin H; Fardeau M
Rev Neurol (Paris); 1978 Jan; 134(1):45-58. PubMed ID: 674985
[TBL] [Abstract][Full Text] [Related]
37. Familial hypokalemic periodic paralysis. 50-year follow-up of a large family.
Buruma OJ; Bots GT; Went LN
Arch Neurol; 1985 Jan; 42(1):28-31. PubMed ID: 3855357
[TBL] [Abstract][Full Text] [Related]
38. Primary periodic paralyses.
Finsterer J
Acta Neurol Scand; 2008 Mar; 117(3):145-58. PubMed ID: 18031562
[TBL] [Abstract][Full Text] [Related]
39. PROGRESSIVE NEUROLOGICAL DISORDER AND MYOTONIA CONGENITA ASSOCIATED WITH PARAMYOTONIA.
HUDSON AJ
Brain; 1963 Dec; 86():811-26. PubMed ID: 14090531
[No Abstract] [Full Text] [Related]
40. Correlating phenotype and genotype in the periodic paralyses.
Miller TM; Dias da Silva MR; Miller HA; Kwiecinski H; Mendell JR; Tawil R; McManis P; Griggs RC; Angelini C; Servidei S; Petajan J; Dalakas MC; Ranum LP; Fu YH; Ptácek LJ
Neurology; 2004 Nov; 63(9):1647-55. PubMed ID: 15534250
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]