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 *

188 related articles for article (PubMed ID: 20628234)

  • 1. A nonsense mutation in the SCN9A gene in congenital insensitivity to pain.
    Kurban M; Wajid M; Shimomura Y; Christiano AM
    Dermatology; 2010; 221(2):179-83. PubMed ID: 20628234
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. Novel SCN9A variant associated with congenital insensitivity to pain.
    Yammine T; Aprahamian R; Souaid M; Salem N; Awwad J; Farra C
    Mol Biol Rep; 2023 Jul; 50(7):6293-6298. PubMed ID: 37231219
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Infrequent SCN9A mutations in congenital insensitivity to pain and erythromelalgia.
    Klein CJ; Wu Y; Kilfoyle DH; Sandroni P; Davis MD; Gavrilova RH; Low PA; Dyck PJ
    J Neurol Neurosurg Psychiatry; 2013 Apr; 84(4):386-91. PubMed ID: 23129781
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Identification of founder and novel mutations that cause congenital insensitivity to pain (CIP) in palestinian patients.
    Khaled B; Alzahayqa M; Jaffal A; Sallam H; Thawabta R; Mansour M; Alian A; Salah Z
    BMC Med Genomics; 2023 May; 16(1):120. PubMed ID: 37248554
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Biallelic truncating SCN9A mutation identified in four families with congenital insensitivity to pain from Pakistan.
    Sawal HA; Harripaul R; Mikhailov A; Dad R; Ayub M; Jawad Hassan M; Vincent JB
    Clin Genet; 2016 Dec; 90(6):563-565. PubMed ID: 27747863
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two novel SCN9A gene heterozygous mutations may cause partial deletion of pain perception.
    Yuan R; Zhang X; Deng Q; Si D; Wu Y; Gao F; Zhou B
    Pain Med; 2011 Oct; 12(10):1510-4. PubMed ID: 21939494
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel SCN9A mutations underlying extreme pain phenotypes: unexpected electrophysiological and clinical phenotype correlations.
    Emery EC; Habib AM; Cox JJ; Nicholas AK; Gribble FM; Woods CG; Reimann F
    J Neurosci; 2015 May; 35(20):7674-81. PubMed ID: 25995458
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusia.
    Marchi M; Provitera V; Nolano M; Romano M; Maccora S; D'Amato I; Salvi E; Gerrits M; Santoro L; Lauria G
    J Peripher Nerv Syst; 2018 Sep; 23(3):202-206. PubMed ID: 29978519
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel mutation in the SCN9A gene associated with congenital insensitivity to pain, anhidrosis, and mild cognitive impairment.
    Romagnuolo M; Moltrasio C; Cavalli R; Brena M; Tadini G
    Pediatr Dermatol; 2024; 41(1):80-83. PubMed ID: 37345838
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SCN9A channelopathy associated autosomal recessive Congenital Indifference to Pain. A case report.
    Rajasekharan S; Martens L; Domingues L; Cauwels R
    Eur J Paediatr Dent; 2017 Mar; 18(1):66-68. PubMed ID: 28494607
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Functional confirmation that the R1488* variant in SCN9A results in complete loss-of-function of Na
    He W; Young GT; Zhang B; Cox PJ; Cho LT; John S; Paciga SA; Wood LS; Danziger N; Scollen S; Vangjeli C
    BMC Med Genet; 2018 Jul; 19(1):124. PubMed ID: 30037327
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Channelopathy: a novel mutation in the SCN9A gene causes insensitivity to pain and autonomic dysregulation.
    Bartholomew F; Lazar J; Marqueling A; Lee-Messer C; Jaradeh S; Teng JM
    Br J Dermatol; 2014 Nov; 171(5):1268-70. PubMed ID: 24813348
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.