165 related articles for article (PubMed ID: 24813348)
1. 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]
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. 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. 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]
5. 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]
6. 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]
7. [Congenital insensitivity to pain].
Inani K; Mernissi F
Pan Afr Med J; 2014; 18():197. PubMed ID: 25419324
[No Abstract] [Full Text] [Related]
8. 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]
9. SCN9A-associated congenital insensitivity to pain and anosmia in an Irish patient.
Bogdanova-Mihaylova P; Alexander MD; Murphy RP; Murphy SM
J Peripher Nerv Syst; 2015 Jun; 20(2):86-7. PubMed ID: 26292973
[No 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. 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]
13. [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]
14. 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]
15. Paroxysmal extreme pain disorder in family with c.3892G > T (p.Val1298Phe) in the SCN9A gene mutation - case report.
Stępień A; Sałacińska D; Staszewski J; Durka-Kęsy M; Dobrogowski J
BMC Neurol; 2020 May; 20(1):182. PubMed ID: 32404070
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
