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Journal Abstract Search

348 related items for PubMed ID: 18803825

  • 1. Paroxysmal extreme pain disorder M1627K mutation in human Nav1.7 renders DRG neurons hyperexcitable.
    Dib-Hajj SD, Estacion M, Jarecki BW, Tyrrell L, Fischer TZ, Lawden M, Cummins TR, Waxman SG.
    Mol Pain; 2008 Sep 19; 4():37. PubMed ID: 18803825
    [Abstract] [Full Text] [Related]

  • 2. NaV1.7 gain-of-function mutations as a continuum: A1632E displays physiological changes associated with erythromelalgia and paroxysmal extreme pain disorder mutations and produces symptoms of both disorders.
    Estacion M, Dib-Hajj SD, Benke PJ, Te Morsche RH, Eastman EM, Macala LJ, Drenth JP, Waxman SG.
    J Neurosci; 2008 Oct 22; 28(43):11079-88. PubMed ID: 18945915
    [Abstract] [Full Text] [Related]

  • 3. Mutations at opposite ends of the DIII/S4-S5 linker of sodium channel Na V 1.7 produce distinct pain disorders.
    Cheng X, Dib-Hajj SD, Tyrrell L, Wright DA, Fischer TZ, Waxman SG.
    Mol Pain; 2010 Apr 29; 6():24. PubMed ID: 20429905
    [Abstract] [Full Text] [Related]

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  • 5. The Domain II S4-S5 Linker in Nav1.9: A Missense Mutation Enhances Activation, Impairs Fast Inactivation, and Produces Human Painful Neuropathy.
    Han C, Yang Y, de Greef BT, Hoeijmakers JG, Gerrits MM, Verhamme C, Qu J, Lauria G, Merkies IS, Faber CG, Dib-Hajj SD, Waxman SG.
    Neuromolecular Med; 2015 Jun 29; 17(2):158-69. PubMed ID: 25791876
    [Abstract] [Full Text] [Related]

  • 6. Nav1.7-A1632G Mutation from a Family with Inherited Erythromelalgia: Enhanced Firing of Dorsal Root Ganglia Neurons Evoked by Thermal Stimuli.
    Yang Y, Huang J, Mis MA, Estacion M, Macala L, Shah P, Schulman BR, Horton DB, Dib-Hajj SD, Waxman SG.
    J Neurosci; 2016 Jul 13; 36(28):7511-22. PubMed ID: 27413160
    [Abstract] [Full Text] [Related]

  • 7. Inherited pain: sodium channel Nav1.7 A1632T mutation causes erythromelalgia due to a shift of fast inactivation.
    Eberhardt M, Nakajima J, Klinger AB, Neacsu C, Hühne K, O'Reilly AO, Kist AM, Lampe AK, Fischer K, Gibson J, Nau C, Winterpacht A, Lampert A.
    J Biol Chem; 2014 Jan 24; 289(4):1971-80. PubMed ID: 24311784
    [Abstract] [Full Text] [Related]

  • 8. Paroxysmal extreme pain disorder mutations within the D3/S4-S5 linker of Nav1.7 cause moderate destabilization of fast inactivation.
    Jarecki BW, Sheets PL, Jackson JO, Cummins TR.
    J Physiol; 2008 Sep 01; 586(17):4137-53. PubMed ID: 18599537
    [Abstract] [Full Text] [Related]

  • 9. Depolarized inactivation overcomes impaired activation to produce DRG neuron hyperexcitability in a Nav1.7 mutation in a patient with distal limb pain.
    Huang J, Yang Y, Dib-Hajj SD, van Es M, Zhao P, Salomon J, Drenth JP, Waxman SG.
    J Neurosci; 2014 Sep 10; 34(37):12328-40. PubMed ID: 25209274
    [Abstract] [Full Text] [Related]

  • 10. Small-fiber neuropathy Nav1.8 mutation shifts activation to hyperpolarized potentials and increases excitability of dorsal root ganglion neurons.
    Huang J, Yang Y, Zhao P, Gerrits MM, Hoeijmakers JG, Bekelaar K, Merkies IS, Faber CG, Dib-Hajj SD, Waxman SG.
    J Neurosci; 2013 Aug 28; 33(35):14087-97. PubMed ID: 23986244
    [Abstract] [Full Text] [Related]

  • 11. Distinct repriming and closed-state inactivation kinetics of Nav1.6 and Nav1.7 sodium channels in mouse spinal sensory neurons.
    Herzog RI, Cummins TR, Ghassemi F, Dib-Hajj SD, Waxman SG.
    J Physiol; 2003 Sep 15; 551(Pt 3):741-50. PubMed ID: 12843211
    [Abstract] [Full Text] [Related]

  • 12. Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7.
    Estacion M, Han C, Choi JS, Hoeijmakers JG, Lauria G, Drenth JP, Gerrits MM, Dib-Hajj SD, Faber CG, Merkies IS, Waxman SG.
    Mol Pain; 2011 Dec 02; 7():92. PubMed ID: 22136189
    [Abstract] [Full Text] [Related]

  • 13. The Novel Activity of Carbamazepine as an Activation Modulator Extends from NaV1.7 Mutations to the NaV1.8-S242T Mutant Channel from a Patient with Painful Diabetic Neuropathy.
    Han C, Themistocleous AC, Estacion M, Dib-Hajj FB, Blesneac I, Macala L, Fratter C, Bennett DL, Waxman SG, Dib-Hajj SD.
    Mol Pharmacol; 2018 Nov 02; 94(5):1256-1269. PubMed ID: 30135145
    [Abstract] [Full Text] [Related]

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  • 15. Genetics and molecular pathophysiology of Na(v)1.7-related pain syndromes.
    Dib-Hajj SD, Yang Y, Waxman SG.
    Adv Genet; 2008 Nov 02; 63():85-110. PubMed ID: 19185186
    [Abstract] [Full Text] [Related]

  • 16. Differential effect of D623N variant and wild-type Na(v)1.7 sodium channels on resting potential and interspike membrane potential of dorsal root ganglion neurons.
    Ahn HS, Vasylyev DV, Estacion M, Macala LJ, Shah P, Faber CG, Merkies IS, Dib-Hajj SD, Waxman SG.
    Brain Res; 2013 Sep 05; 1529():165-77. PubMed ID: 23850641
    [Abstract] [Full Text] [Related]

  • 17. p.L1612P, a novel voltage-gated sodium channel Nav1.7 mutation inducing a cold sensitive paroxysmal extreme pain disorder.
    Suter MR, Bhuiyan ZA, Laedermann CJ, Kuntzer T, Schaller M, Stauffacher MW, Roulet E, Abriel H, Decosterd I, Wider C.
    Anesthesiology; 2015 Feb 05; 122(2):414-23. PubMed ID: 25285947
    [Abstract] [Full Text] [Related]

  • 18. Effects of ranolazine on wild-type and mutant hNav1.7 channels and on DRG neuron excitability.
    Estacion M, Waxman SG, Dib-Hajj SD.
    Mol Pain; 2010 Jun 08; 6():35. PubMed ID: 20529343
    [Abstract] [Full Text] [Related]

  • 19. Ca2+ toxicity due to reverse Na+/Ca2+ exchange contributes to degeneration of neurites of DRG neurons induced by a neuropathy-associated Nav1.7 mutation.
    Estacion M, Vohra BP, Liu S, Hoeijmakers J, Faber CG, Merkies IS, Lauria G, Black JA, Waxman SG.
    J Neurophysiol; 2015 Sep 08; 114(3):1554-64. PubMed ID: 26156380
    [Abstract] [Full Text] [Related]

  • 20. Mutation I136V alters electrophysiological properties of the Na(v)1.7 channel in a family with onset of erythromelalgia in the second decade.
    Cheng X, Dib-Hajj SD, Tyrrell L, Waxman SG.
    Mol Pain; 2008 Jan 02; 4():1. PubMed ID: 18171466
    [Abstract] [Full Text] [Related]

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