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4. Enhanced slow inactivation by V445M: a sodium channel mutation associated with myotonia. Takahashi MP; Cannon SC Biophys J; 1999 Feb; 76(2):861-8. PubMed ID: 9929487 [TBL] [Abstract][Full Text] [Related]
5. Sodium channel defects in myotonia and periodic paralysis. Cannon SC Annu Rev Neurosci; 1996; 19():141-64. PubMed ID: 8833439 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Mexiletine block of disease-associated mutations in S6 segments of the human skeletal muscle Na(+) channel. Takahashi MP; Cannon SC J Physiol; 2001 Dec; 537(Pt 3):701-14. PubMed ID: 11744749 [TBL] [Abstract][Full Text] [Related]
8. A global defect in scaling relationship between electrical activity and availability of muscle sodium channels in hyperkalemic periodic paralysis. Melamed-Frank M; Marom S Pflugers Arch; 1999 Jul; 438(2):213-7. PubMed ID: 10370108 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Loss of Na+ channel inactivation by anemone toxin (ATX II) mimics the myotonic state in hyperkalaemic periodic paralysis. Cannon SC; Corey DP J Physiol; 1993 Jul; 466():501-20. PubMed ID: 8105077 [TBL] [Abstract][Full Text] [Related]
11. A C-terminal skeletal muscle sodium channel mutation associated with myotonia disrupts fast inactivation. Wu FF; Gordon E; Hoffman EP; Cannon SC J Physiol; 2005 Jun; 565(Pt 2):371-80. PubMed ID: 15774523 [TBL] [Abstract][Full Text] [Related]
12. Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation. Bendahhou S; Cummins TR; Tawil R; Waxman SG; Ptácek LJ J Neurosci; 1999 Jun; 19(12):4762-71. PubMed ID: 10366610 [TBL] [Abstract][Full Text] [Related]
14. Human sodium channel gating defects caused by missense mutations in S6 segments associated with myotonia: S804F and V1293I. Green DS; George AL; Cannon SC J Physiol; 1998 Aug; 510 ( Pt 3)(Pt 3):685-94. PubMed ID: 9660885 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]