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There are 142274 results for: content related to: Erythromelalgia

  1. No mutations in the voltage-gated NaV1.7 sodium channel α1 subunit gene SCN9A in familial complex regional pain syndrome

    European Journal of Neurology

    Volume 17, Issue 6, June 2010, Pages: 808–814, A. M. De Rooij, M. F. Gosso, E. Alsina-Sanchis, J. Marinus, J. J. Van Hilten and A. M. J. M. Van Den Maagdenberg

    Version of Record online : 13 JAN 2010, DOI: 10.1111/j.1468-1331.2009.02931.x

  2. Abnormal Pain Conditions in Humans Related to Genetic Mutations

    Pain Genetics: Basic to Translational Science

    Inna Belfer, Luda Diatchenko, Pages: 61–77, 2013

    Published Online : 22 NOV 2013, DOI: 10.1002/9781118398890.ch5

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    Human Mendelian pain disorders: a key to discovery and validation of novel analgesics

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 367–373, YP Goldberg, SN Pimstone, R Namdari, N Price, C Cohen, RP Sherrington and MR Hayden

    Version of Record online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01942.x

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    A Nav1.7 channel mutation associated with hereditary erythromelalgia contributes to neuronal hyperexcitability and displays reduced lidocaine sensitivity

    The Journal of Physiology

    Volume 581, Issue 3, June 2007, Pages: 1019–1031, Patrick L. Sheets, James O. Jackson II, Stephen G. Waxman, Sulayman D. Dib-Hajj and Theodore R. Cummins

    Version of Record online : 6 JUN 2007, DOI: 10.1113/jphysiol.2006.127027

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    Genetic aspects of sodium channelopathy in small fiber neuropathy

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 351–358, JGJ Hoeijmakers, ISJ Merkies, MM Gerrits, SG Waxman and CG Faber

    Version of Record online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01937.x

  6. An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorder

    Muscle & Nerve

    Volume 49, Issue 1, January 2014, Pages: 134–138, Inge Anita Meijer, Michel Vanasse, Sonia Nizard, Yves Robitaille and Elsa Rossignol

    Version of Record online : 22 NOV 2013, DOI: 10.1002/mus.23968

  7. Erythromelalgia with a linear pattern in a 12-year-old girl

    Pediatrics International

    Volume 57, Issue 4, August 2015, Pages: 706–708, Seokwon Huh, Mo Kyung Jung, Lucy Youngmin Eun, Jo Won Jung and Jae Young Choi

    Version of Record online : 28 AUG 2015, DOI: 10.1111/ped.12661

  8. Recurrent Facial Erythema with Burning Sensation and Increased Temperature: A Variant of Erythromelalgia or a New Entity?

    Pain Medicine

    Volume 15, Issue 6, June 2014, Pages: 1007–1010, Di-Qing Luo, Yu-Kun Zhao, Qing-Fang Xu, Xiang-Qun He and Liang-Cai Wu

    Version of Record online : 16 JAN 2014, DOI: 10.1111/pme.12343

  9. You have full text access to this OnlineOpen article
    Na+ current properties in islet α- and β-cells reflect cell-specific Scn3a and Scn9a expression

    The Journal of Physiology

    Volume 592, Issue 21, 1 November 2014, Pages: 4677–4696, Quan Zhang, Margarita V. Chibalina, Martin Bengtsson, Lukas N. Groschner, Reshma Ramracheya, Nils J. G. Rorsman, Veronika Leiss, Mohammed A. Nassar, Andrea Welling, Fiona M. Gribble, Frank Reimann, Franz Hofmann, John N. Wood, Frances M. Ashcroft and Patrik Rorsman

    Version of Record online : 31 OCT 2014, DOI: 10.1113/jphysiol.2014.274209

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    Voltage-Gated Sodium Channels: Therapeutic Targets for Pain

    Pain Medicine

    Volume 10, Issue 7, October 2009, Pages: 1260–1269, Sulayman D. Dib-Hajj, Joel A. Black and Stephen G. Waxman

    Version of Record online : 6 OCT 2009, DOI: 10.1111/j.1526-4637.2009.00719.x

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    Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome


    Volume 54, Issue 9, September 2013, Pages: e122–e126, John C. Mulley, Bree Hodgson, Jacinta M. McMahon, Xenia Iona, Susannah Bellows, Saul A Mullen, Kevin Farrell, Mark Mackay, Lynette Sadleir, Andrew Bleasel, Deepak Gill, Richard Webster, Elaine C. Wirrell, Michael Harbord, Sanyjay Sisodiya, Eva Andermann, Sara Kivity, Samuel F. Berkovic, Ingrid E. Scheffer and Leanne M. Dibbens

    Version of Record online : 29 JUL 2013, DOI: 10.1111/epi.12323

  12. Two Novel SCN9A Gene Heterozygous Mutations May Cause Partial Deletion of Pain Perception

    Pain Medicine

    Volume 12, Issue 10, October 2011, Pages: 1510–1514, Ruimei Yuan, Xianwei Zhang, Qian Deng, Dayong Si, Yuan Wu, Feng Gao and Biyun Zhou

    Version of Record online : 21 SEP 2011, DOI: 10.1111/j.1526-4637.2011.01237.x

  13. You have full text access to this OnlineOpen article
    Mexiletine as a treatment for primary erythromelalgia: normalization of biophysical properties of mutant L858F NaV1.7 sodium channels

    British Journal of Pharmacology

    Volume 171, Issue 19, October 2014, Pages: 4455–4463, R Cregg, J J Cox, D L H Bennett, J N Wood and R Werdehausen

    Version of Record online : 29 AUG 2014, DOI: 10.1111/bph.12788

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    Paroxysmal extreme pain disorder mutations within the D3/S4–S5 linker of Nav1.7 cause moderate destabilization of fast inactivation

    The Journal of Physiology

    Volume 586, Issue 17, September 2008, Pages: 4137–4153, Brian W. Jarecki, Patrick L. Sheets, James O. Jackson II and Theodore R. Cummins

    Version of Record online : 10 SEP 2008, DOI: 10.1113/jphysiol.2008.154906

  15. A sodium channel gene SCN9A polymorphism that increases nociceptor excitability

    Annals of Neurology

    Volume 66, Issue 6, December 2009, Pages: 862–866, Mark Estacion, T. Patrick Harty, Jin-Sung Choi, Lynda Tyrrell, Sulayman D. Dib-Hajj and Stephen G. Waxman

    Version of Record online : 13 OCT 2009, DOI: 10.1002/ana.21895

  16. Erythromelalgia: A hereditary pain syndrome enters the molecular era

    Annals of Neurology

    Volume 57, Issue 6, June 2005, Pages: 785–788, Stephen G. Waxman and Sulayman D. Dib-Hajj

    Version of Record online : 31 MAY 2005, DOI: 10.1002/ana.20511

  17. Channelopathy: a novel mutation in the SCN9A gene causes insensitivity to pain and autonomic dysregulation

    British Journal of Dermatology

    Volume 171, Issue 5, November 2014, Pages: 1268–1270, F. Bartholomew, J. Lazar, A. Marqueling, C. Lee-Messer, S. Jaradeh and J. M. C. Teng

    Version of Record online : 19 OCT 2014, DOI: 10.1111/bjd.13096


    International Journal of Dermatology

    Volume 34, Issue 2, February 1995, Pages: 97–100, JAN JACQUES MICHIELS, JOOST P.H. DRENTH and PERRY J.J. VAN GENDEREN

    Version of Record online : 31 MAY 2007, DOI: 10.1111/j.1365-4362.1995.tb03587.x

  19. Familial pain syndromes from mutations of the Nav1.7 sodium channel

    Annals of the New York Academy of Sciences

    Volume 1184, Issue 1, January 2010, Pages: 196–207, Tanya Z. Fischer and Stephen G. Waxman

    Version of Record online : 24 NOV 2009, DOI: 10.1111/j.1749-6632.2009.05110.x

  20. Treatment of familial erythromelalgia with venlafaxine

    Journal of the European Academy of Dermatology and Venereology

    Volume 21, Issue 6, July 2007, Pages: 836–837, D Firmin, AM Roguedas, M Greco, C Morvan, D Legoupil, C Fleuret and L Misery

    Version of Record online : 9 JAN 2007, DOI: 10.1111/j.1468-3083.2006.02039.x