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.
159 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]
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]