278 related articles for article (PubMed ID: 21891927)
1. Expression patterns of two potassium channel genes in skeletal muscle cells of patients with familial hypokalemic periodic paralysis.
Kim JB; Lee GM; Kim SJ; Yoon DH; Lee YH
Neurol India; 2011; 59(4):527-31. PubMed ID: 21891927
[TBL] [Abstract][Full Text] [Related]
2. Reduced expression and abnormal localization of the K(ATP) channel subunit SUR2A in patients with familial hypokalemic periodic paralysis.
Kim SJ; Lee YJ; Kim JB
Biochem Biophys Res Commun; 2010 Jan; 391(1):974-8. PubMed ID: 19962959
[TBL] [Abstract][Full Text] [Related]
3. Mutation screening in Chinese hypokalemic periodic paralysis patients.
Wang W; Jiang L; Ye L; Zhu N; Su T; Guan L; Li X; Ning G
Mol Genet Metab; 2006 Apr; 87(4):359-63. PubMed ID: 16386935
[TBL] [Abstract][Full Text] [Related]
4. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.
Ke T; Gomez CR; Mateus HE; Castano JA; Wang QK
J Hum Genet; 2009 Nov; 54(11):660-4. PubMed ID: 19779499
[TBL] [Abstract][Full Text] [Related]
5. The large-conductance calcium-activated potassium channel holds the key to the conundrum of familial hypokalemic periodic paralysis.
Kim JB; Kim SJ; Kang SY; Yi JW; Kim SM
Korean J Pediatr; 2014 Oct; 57(10):445-50. PubMed ID: 25379045
[TBL] [Abstract][Full Text] [Related]
6. [From gene to diseases; hypokalemic periodic paralysis].
Links TP; Ginjaar HB; van der Hoeven JH
Ned Tijdschr Geneeskd; 2004 May; 148(21):1035-8. PubMed ID: 15185439
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family.
Incecik F; Hergüner MO; Altunbaşak S; Lehman-Horn F
Turk J Pediatr; 2010; 52(4):409-10. PubMed ID: 21043388
[TBL] [Abstract][Full Text] [Related]
9. Molecular basis for hyperkalemic periodic paralysis.
Brown RH
Int J Neurol; 1991-1992; 25-26():89-96. PubMed ID: 11980067
[TBL] [Abstract][Full Text] [Related]
10. Enhancement of K+ conductance improves in vitro the contraction force of skeletal muscle in hypokalemic periodic paralysis.
Grafe P; Quasthoff S; Strupp M; Lehmann-Horn F
Muscle Nerve; 1990 May; 13(5):451-7. PubMed ID: 2345562
[TBL] [Abstract][Full Text] [Related]
11. Insulin acts in hypokalemic periodic paralysis by reducing inward rectifier K+ current.
Ruff RL
Neurology; 1999 Oct; 53(7):1556-63. PubMed ID: 10534267
[TBL] [Abstract][Full Text] [Related]
12. Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis.
Kil TH; Kim JB
Eur J Paediatr Neurol; 2010 May; 14(3):278-81. PubMed ID: 19822448
[TBL] [Abstract][Full Text] [Related]
13. Muscle weakness in a Japanese family of Arg1239His mutation hypokalemic periodic paralysis.
Kusumi M; Kumada H; Adachi Y; Nakashima K
Psychiatry Clin Neurosci; 2001 Oct; 55(5):539-41. PubMed ID: 11555352
[TBL] [Abstract][Full Text] [Related]
14. A novel mutation in the calcium channel gene in a family with hypokalemic periodic paralysis.
Hirano M; Kokunai Y; Nagai A; Nakamura Y; Saigoh K; Kusunoki S; Takahashi MP
J Neurol Sci; 2011 Oct; 309(1-2):9-11. PubMed ID: 21855088
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Extracellular potassium homeostasis: insights from hypokalemic periodic paralysis.
Cheng CJ; Kuo E; Huang CL
Semin Nephrol; 2013 May; 33(3):237-47. PubMed ID: 23953801
[TBL] [Abstract][Full Text] [Related]
17. Hypokalemic periodic paralysis as a manifestation of thyrotoxicosis.
Paiboonpol S
J Med Assoc Thai; 2008 Sep; 91(9):1331-5. PubMed ID: 18843860
[TBL] [Abstract][Full Text] [Related]
18. A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis.
Dias Da Silva MR; Cerutti JM; Arnaldi LA; Maciel RM
J Clin Endocrinol Metab; 2002 Nov; 87(11):4881-4. PubMed ID: 12414843
[TBL] [Abstract][Full Text] [Related]
19. Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current.
Jurkat-Rott K; Mitrovic N; Hang C; Kouzmekine A; Iaizzo P; Herzog J; Lerche H; Nicole S; Vale-Santos J; Chauveau D; Fontaine B; Lehmann-Horn F
Proc Natl Acad Sci U S A; 2000 Aug; 97(17):9549-54. PubMed ID: 10944223
[TBL] [Abstract][Full Text] [Related]
20. INa and IKir are reduced in Type 1 hypokalemic and thyrotoxic periodic paralysis.
Puwanant A; Ruff RL
Muscle Nerve; 2010 Sep; 42(3):315-27. PubMed ID: 20589886
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]