221 related articles for article (PubMed ID: 18317596)
1. Targeted mutation of mouse skeletal muscle sodium channel produces myotonia and potassium-sensitive weakness.
Hayward LJ; Kim JS; Lee MY; Zhou H; Kim JW; Misra K; Salajegheh M; Wu FF; Matsuda C; Reid V; Cros D; Hoffman EP; Renaud JM; Cannon SC; Brown RH
J Clin Invest; 2008 Apr; 118(4):1437-49. PubMed ID: 18317596
[TBL] [Abstract][Full Text] [Related]
2. Contractile abnormalities of mouse muscles expressing hyperkalemic periodic paralysis mutant NaV1.4 channels do not correlate with Na+ influx or channel content.
Lucas B; Ammar T; Khogali S; DeJong D; Barbalinardo M; Nishi C; Hayward LJ; Renaud JM
Physiol Genomics; 2014 Jun; 46(11):385-97. PubMed ID: 24714718
[TBL] [Abstract][Full Text] [Related]
3. Na+,K+-pump stimulation improves contractility in isolated muscles of mice with hyperkalemic periodic paralysis.
Clausen T; Nielsen OB; Clausen JD; Pedersen TH; Hayward LJ
J Gen Physiol; 2011 Jul; 138(1):117-30. PubMed ID: 21708955
[TBL] [Abstract][Full Text] [Related]
4. Understanding the physiology of the asymptomatic diaphragm of the M1592V hyperkalemic periodic paralysis mouse.
Ammar T; Lin W; Higgins A; Hayward LJ; Renaud JM
J Gen Physiol; 2015 Dec; 146(6):509-25. PubMed ID: 26621775
[TBL] [Abstract][Full Text] [Related]
5. Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis.
Jurkat-Rott K; Lehmann-Horn F
Neurotherapeutics; 2007 Apr; 4(2):216-24. PubMed ID: 17395131
[TBL] [Abstract][Full Text] [Related]
6. A sodium channel knockin mutant (NaV1.4-R669H) mouse model of hypokalemic periodic paralysis.
Wu F; Mi W; Burns DK; Fu Y; Gray HF; Struyk AF; Cannon SC
J Clin Invest; 2011 Oct; 121(10):4082-94. PubMed ID: 21881211
[TBL] [Abstract][Full Text] [Related]
7. Cold-induced defects of sodium channel gating in atypical periodic paralysis plus myotonia.
Webb J; Cannon SC
Neurology; 2008 Mar; 70(10):755-61. PubMed ID: 17898326
[TBL] [Abstract][Full Text] [Related]
8. Spectrum of sodium channel disturbances in the nondystrophic myotonias and periodic paralyses.
Cannon SC
Kidney Int; 2000 Mar; 57(3):772-9. PubMed ID: 10720928
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker.
Hayward LJ; Brown RH; Cannon SC
J Gen Physiol; 1996 May; 107(5):559-76. PubMed ID: 8740371
[TBL] [Abstract][Full Text] [Related]
11. A Mixed Periodic Paralysis & Myotonia Mutant, P1158S, Imparts pH-Sensitivity in Skeletal Muscle Voltage-gated Sodium Channels.
Ghovanloo MR; Abdelsayed M; Peters CH; Ruben PC
Sci Rep; 2018 Apr; 8(1):6304. PubMed ID: 29674667
[TBL] [Abstract][Full Text] [Related]
12. Skeletal muscle channelopathies.
Jurkat-Rott K; Lerche H; Lehmann-Horn F
J Neurol; 2002 Nov; 249(11):1493-502. PubMed ID: 12420087
[TBL] [Abstract][Full Text] [Related]
13. The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation.
Struyk AF; Scoggan KA; Bulman DE; Cannon SC
J Neurosci; 2000 Dec; 20(23):8610-7. PubMed ID: 11102465
[TBL] [Abstract][Full Text] [Related]
14. Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis.
Hayward LJ; Brown RH; Cannon SC
Biophys J; 1997 Mar; 72(3):1204-19. PubMed ID: 9138567
[TBL] [Abstract][Full Text] [Related]
15. Mechanisms of a human skeletal myotonia produced by mutation in the C-terminus of NaV1.4: is Ca2+ regulation defective?
Biswas S; DiSilvestre DA; Dong P; Tomaselli GF
PLoS One; 2013; 8(12):e81063. PubMed ID: 24324661
[TBL] [Abstract][Full Text] [Related]
16. Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis.
Ptáĉek LJ; Tawil R; Griggs RC; Meola G; McManis P; Barohn RJ; Mendell JR; Harris C; Spitzer R; Santiago F
Neurology; 1994 Aug; 44(8):1500-3. PubMed ID: 8058156
[TBL] [Abstract][Full Text] [Related]
17. Muscle Na+ channelopathies: MRI detects intracellular 23Na accumulation during episodic weakness.
Weber MA; Nielles-Vallespin S; Essig M; Jurkat-Rott K; Kauczor HU; Lehmann-Horn F
Neurology; 2006 Oct; 67(7):1151-8. PubMed ID: 16931510
[TBL] [Abstract][Full Text] [Related]
18. K(+)-aggravated myotonia: destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation.
Mitrović N; George AL; Heine R; Wagner S; Pika U; Hartlaub U; Zhou M; Lerche H; Fahlke C; Lehmann-Horn F
J Physiol; 1994 Aug; 478 Pt 3(Pt 3):395-402. PubMed ID: 7965854
[TBL] [Abstract][Full Text] [Related]
19. Disappearance of episodic weakness during pregnancy in hyperkalemic periodic paralysis from the SCNA4 mutation T704M.
Finsterer J
Neurologist; 2009 Sep; 15(5):289-90. PubMed ID: 19741438
[TBL] [Abstract][Full Text] [Related]
20. Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5.
Bendahhou S; Cummins TR; Kula RW; Fu YH; Ptácek LJ
Neurology; 2002 Apr; 58(8):1266-72. PubMed ID: 11971097
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]