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Results: 1-8 |
Results: 8
Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis
Authors: Bendahhou, S Cummins, TR Griggs, RC Fu, YH Ptacek, LJ
Citation: S. Bendahhou et al., Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis, ANN NEUROL, 50(3), 2001, pp. 417-420
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
Authors: Plaster, NM Tawil, R Tristani-Firouzi, M Canun, S Bendahhou, S Tsunoda, A Donaldson, MR Iannaccone, ST Brunt, E Barohn, R Clark, J Deymeer, F George, AL Fish, FA Hahn, A Nitu, A Ozdemir, C Serdaroglu, P Subramony, SH Wolfe, G Fu, YH Ptacek, LJ
Citation: Nm. Plaster et al., Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome, CELL, 105(4), 2001, pp. 511-519
MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis
Authors: Abbott, GW Butler, MH Bendahhou, S Dalakas, MC Ptacek, LJ Goldstein, SAN
Citation: Gw. Abbott et al., MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis, CELL, 104(2), 2001, pp. 217-231
Functional consequences of chloride channel gene (CLCN1) mutations causingmyotonia congenita
Authors: Zhang, J Bendahhou, S Sanguinetti, MC Ptacek, LJ
Citation: J. Zhang et al., Functional consequences of chloride channel gene (CLCN1) mutations causingmyotonia congenita, NEUROLOGY, 54(4), 2000, pp. 937-942
A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation
Authors: Bendahhou, S Cummins, TR Hahn, AF Langlois, S Waxman, SG Ptacek, LJ
Citation: S. Bendahhou et al., A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation, J CLIN INV, 106(3), 2000, pp. 431-438
Activation and inactivation of the voltage-gated sodium channel: Role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation
Authors: Bendahhou, S Cummins, TR Tawil, R Waxman, SG Ptacek, LJ
Citation: S. Bendahhou et al., Activation and inactivation of the voltage-gated sodium channel: Role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation, J NEUROSC, 19(12), 1999, pp. 4762-4771
Characterization of a new sodium channel mutation at arginine 1448 associated with moderate paramyotonia, congenita in humans
Authors: Bendahhou, S Cummins, TR Kwiecinski, H Waxman, SG Ptacek, LJ
Citation: S. Bendahhou et al., Characterization of a new sodium channel mutation at arginine 1448 associated with moderate paramyotonia, congenita in humans, J PHYSL LON, 518(2), 1999, pp. 337-344
Sodium channel fragments: Contributions to voltage sensitivity and ion selectivity
Authors: Duclohier, H Helluin, O Cosette, P Bendahhou, S
Citation: H. Duclohier et al., Sodium channel fragments: Contributions to voltage sensitivity and ion selectivity, BIOSCI REP, 18(6), 1998, pp. 279-286
Risultati: 1-8 |