BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 37231219)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. SCN9A variant in a family of mixed breed dogs with congenital insensitivity to pain.
    Gutierrez-Quintana R; Christen M; Faller KME; Guevar J; Jagannathan V; Leeb T
    J Vet Intern Med; 2023 Jan; 37(1):230-235. PubMed ID: 36630088
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Novel compound heterozygous SCN9A variations causing congenital insensitivity to pain in a patient].
    Bai Y; Sun Y; Wu J; Liu N; Jiao Z; Li Q; Zhao K; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Apr; 39(4):392-396. PubMed ID: 35446973
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Congenital insensitivity to pain: a novel mutation affecting a U12-type intron causes multiple aberrant splicing of SCN9A.
    Marchi M; D'Amato I; Andelic M; Cartelli D; Salvi E; Lombardi R; Gumus E; Lauria G
    Pain; 2022 Jul; 163(7):e882-e887. PubMed ID: 34799533
    [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. 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]  

  • 16. Ocular manifestations among patients with congenital insensitivity to pain due to variants in PRDM12 and SCN9A genes.
    Elsana B; Imtirat A; Yagev R; Gradstein L; Majdalani P; Iny O; Parvari R; Tsumi E
    Am J Med Genet A; 2022 Dec; 188(12):3463-3468. PubMed ID: 36111846
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Charcot ankle, congenital insensitivity to pain and a mutation in the SCN9A gene.
    Chen Z; Zhang H; Dai SM
    QJM; 2022 Jul; 115(7):469-470. PubMed ID: 35512413
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.