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Journal Abstract Search

214 related items for PubMed ID: 19185186

  • 1. Genetics and molecular pathophysiology of Na(v)1.7-related pain syndromes.
    Dib-Hajj SD, Yang Y, Waxman SG.
    Adv Genet; 2008; 63():85-110. PubMed ID: 19185186
    [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. Na(V)1.7 mutant A863P in erythromelalgia: effects of altered activation and steady-state inactivation on excitability of nociceptive dorsal root ganglion neurons.
    Harty TP, Dib-Hajj SD, Tyrrell L, Blackman R, Hisama FM, Rose JB, Waxman SG.
    J Neurosci; 2006 Nov 29; 26(48):12566-75. PubMed ID: 17135418
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. 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]

  • 6. Pain disorders and erythromelalgia caused by voltage-gated sodium channel mutations.
    Dabby R.
    Curr Neurol Neurosci Rep; 2012 Feb 29; 12(1):76-83. PubMed ID: 21984269
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. 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]

  • 9. Voltage-gated sodium channels: therapeutic targets for pain.
    Dib-Hajj SD, Black JA, Waxman SG.
    Pain Med; 2009 Oct 02; 10(7):1260-9. PubMed ID: 19818036
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Familial pain syndromes from mutations of the NaV1.7 sodium channel.
    Fischer TZ, Waxman SG.
    Ann N Y Acad Sci; 2010 Jan 24; 1184():196-207. PubMed ID: 20146699
    [Abstract] [Full Text] [Related]

  • 12. Small nerve fibres, small hands and small feet: a new syndrome of pain, dysautonomia and acromesomelia in a kindred with a novel NaV1.7 mutation.
    Hoeijmakers JG, Han C, Merkies IS, Macala LJ, Lauria G, Gerrits MM, Dib-Hajj SD, Faber CG, Waxman SG.
    Brain; 2012 Feb 24; 135(Pt 2):345-58. PubMed ID: 22286749
    [Abstract] [Full Text] [Related]

  • 13. Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgia.
    Choi JS, Cheng X, Foster E, Leffler A, Tyrrell L, Te Morsche RH, Eastman EM, Jansen HJ, Huehne K, Nau C, Dib-Hajj SD, Drenth JP, Waxman SG.
    Brain; 2010 Jun 24; 133(Pt 6):1823-35. PubMed ID: 20478850
    [Abstract] [Full Text] [Related]

  • 14. From genes to pain: Na v 1.7 and human pain disorders.
    Dib-Hajj SD, Cummins TR, Black JA, Waxman SG.
    Trends Neurosci; 2007 Nov 24; 30(11):555-63. PubMed ID: 17950472
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Alternative splicing of Na(V)1.7 exon 5 increases the impact of the painful PEPD mutant channel I1461T.
    Jarecki BW, Sheets PL, Xiao Y, Jackson JO, Cummins TR.
    Channels (Austin); 2009 Jan 02; 3(4):259-67. PubMed ID: 19633428
    [Abstract] [Full Text] [Related]

  • 17. Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders.
    Drenth JP, Waxman SG.
    J Clin Invest; 2007 Dec 02; 117(12):3603-9. PubMed ID: 18060017
    [Abstract] [Full Text] [Related]

  • 18. Treatment of Na(v)1.7-mediated pain in inherited erythromelalgia using a novel sodium channel blocker.
    Goldberg YP, Price N, Namdari R, Cohen CJ, Lamers MH, Winters C, Price J, Young CE, Verschoof H, Sherrington R, Pimstone SN, Hayden MR.
    Pain; 2012 Jan 02; 153(1):80-85. PubMed ID: 22035805
    [Abstract] [Full Text] [Related]

  • 19. Inherited erythromelalgia due to mutations in SCN9A: natural history, clinical phenotype and somatosensory profile.
    McDonnell A, Schulman B, Ali Z, Dib-Hajj SD, Brock F, Cobain S, Mainka T, Vollert J, Tarabar S, Waxman SG.
    Brain; 2016 Apr 02; 139(Pt 4):1052-65. PubMed ID: 26920677
    [Abstract] [Full Text] [Related]

  • 20. 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]

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