These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 19304393)

  • 1. Two novel SCN9A mutations causing insensitivity to pain.
    Nilsen KB; Nicholas AK; Woods CG; Mellgren SI; Nebuchennykh M; Aasly J
    Pain; 2009 May; 143(1-2):155-8. PubMed ID: 19304393
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations.
    Goldberg YP; MacFarlane J; MacDonald ML; Thompson J; Dube MP; Mattice M; Fraser R; Young C; Hossain S; Pape T; Payne B; Radomski C; Donaldson G; Ives E; Cox J; Younghusband HB; Green R; Duff A; Boltshauser E; Grinspan GA; Dimon JH; Sibley BG; Andria G; Toscano E; Kerdraon J; Bowsher D; Pimstone SN; Samuels ME; Sherrington R; Hayden MR
    Clin Genet; 2007 Apr; 71(4):311-9. PubMed ID: 17470132
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel mutation in SCN9A in a child with congenital insensitivity to pain.
    Shorer Z; Wajsbrot E; Liran TH; Levy J; Parvari R
    Pediatr Neurol; 2014 Jan; 50(1):73-6. PubMed ID: 24188911
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Bilateral congenital corneal anesthesia in a patient with SCN9A mutation, confirmed primary erythromelalgia, and paroxysmal extreme pain disorder.
    Kim DT; Rossignol E; Najem K; Ospina LH
    J AAPOS; 2015 Oct; 19(5):478-9. PubMed ID: 26486037
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Link between pain and olfaction in an inherited sodium channelopathy.
    Zufall F; Pyrski M; Weiss J; Leinders-Zufall T
    Arch Neurol; 2012 Sep; 69(9):1119-23. PubMed ID: 22733046
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Painful Na-channelopathies: an expanding universe.
    Waxman SG
    Trends Mol Med; 2013 Jul; 19(7):406-9. PubMed ID: 23664154
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A stop codon mutation in SCN9A causes lack of pain sensation.
    Ahmad S; Dahllund L; Eriksson AB; Hellgren D; Karlsson U; Lund PE; Meijer IA; Meury L; Mills T; Moody A; Morinville A; Morten J; O'donnell D; Raynoschek C; Salter H; Rouleau GA; Krupp JJ
    Hum Mol Genet; 2007 Sep; 16(17):2114-21. PubMed ID: 17597096
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Chronic non-paroxysmal neuropathic pain - Novel phenotype of mutation in the sodium channel SCN9A gene.
    Dabby R; Sadeh M; Gilad R; Lampl Y; Cohen S; Inbar S; Leshinsky-Silver E
    J Neurol Sci; 2011 Feb; 301(1-2):90-2. PubMed ID: 21094958
    [TBL] [Abstract][Full Text] [Related]  

  • 9. No mutations in the voltage-gated NaV1.7 sodium channel alpha1 subunit gene SCN9A in familial complex regional pain syndrome.
    de Rooij AM; Gosso MF; Alsina-Sanchis E; Marinus J; van Hilten JJ; van den Maagdenberg AM
    Eur J Neurol; 2010 Jun; 17(6):808-14. PubMed ID: 20074229
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel nonsense mutation in SCN9A in a Moroccan child with congenital insensitivity to pain.
    Mansouri M; Chafai Elalaoui S; Ouled Amar Bencheikh B; El Alloussi M; Dion PA; Sefiani A; Rouleau GA
    Pediatr Neurol; 2014 Nov; 51(5):741-4. PubMed ID: 25439579
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two novel mutations of SCN9A (Nav1.7) are associated with partial congenital insensitivity to pain.
    Staud R; Price DD; Janicke D; Andrade E; Hadjipanayis AG; Eaton WT; Kaplan L; Wallace MR
    Eur J Pain; 2011 Mar; 15(3):223-30. PubMed ID: 20692858
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel
    Sun J; Li L; Yang L; Duan G; Ma T; Li N; Liu Y; Yao J; Liu JY; Zhang X
    Mol Pain; 2020; 16():1744806920923881. PubMed ID: 32420800
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. Abnormal expression of voltage-gated sodium channels Nav1.7, Nav1.3 and Nav1.8 in trigeminal neuralgia.
    Siqueira SR; Alves B; Malpartida HM; Teixeira MJ; Siqueira JT
    Neuroscience; 2009 Dec; 164(2):573-7. PubMed ID: 19699781
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Treatment with carbamazepine and gabapentin of a patient with primary erythermalgia (erythromelalgia) identified to have a mutation in the SCN9A gene, encoding a voltage-gated sodium channel.
    Natkunarajah J; Atherton D; Elmslie F; Mansour S; Mortimer P
    Clin Exp Dermatol; 2009 Dec; 34(8):e640-2. PubMed ID: 19549232
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An SCN9A channelopathy causes congenital inability to experience pain.
    Cox JJ; Reimann F; Nicholas AK; Thornton G; Roberts E; Springell K; Karbani G; Jafri H; Mannan J; Raashid Y; Al-Gazali L; Hamamy H; Valente EM; Gorman S; Williams R; McHale DP; Wood JN; Gribble FM; Woods CG
    Nature; 2006 Dec; 444(7121):894-8. PubMed ID: 17167479
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Linkage analysis and functional evaluation of inherited clinical pain conditions.
    Krupp JJ; Hellgren D; Eriksson AB
    Methods Mol Biol; 2010; 617():309-25. PubMed ID: 20336431
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human Mendelian pain disorders: a key to discovery and validation of novel analgesics.
    Goldberg YP; Pimstone SN; Namdari R; Price N; Cohen C; Sherrington RP; Hayden MR
    Clin Genet; 2012 Oct; 82(4):367-73. PubMed ID: 22845492
    [TBL] [Abstract][Full Text] [Related]  

  • 19. How do mutant Nav1.1 sodium channels cause epilepsy?
    Ragsdale DS
    Brain Res Rev; 2008 Jun; 58(1):149-59. PubMed ID: 18342948
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital insensitivity to pain: novel SCN9A missense and in-frame deletion mutations.
    Cox JJ; Sheynin J; Shorer Z; Reimann F; Nicholas AK; Zubovic L; Baralle M; Wraige E; Manor E; Levy J; Woods CG; Parvari R
    Hum Mutat; 2010 Sep; 31(9):E1670-86. PubMed ID: 20635406
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.