227 related articles for article (PubMed ID: 32219415)
1. Understanding the genetic basis of congenital insensitivity to pain.
Drissi I; Woods WA; Woods CG
Br Med Bull; 2020 May; 133(1):65-78. PubMed ID: 32219415
[TBL] [Abstract][Full Text] [Related]
2. New Mendelian Disorders of Painlessness.
Nahorski MS; Chen YC; Woods CG
Trends Neurosci; 2015 Nov; 38(11):712-724. PubMed ID: 26549885
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Defining the Functional Role of Na
McDermott LA; Weir GA; Themistocleous AC; Segerdahl AR; Blesneac I; Baskozos G; Clark AJ; Millar V; Peck LJ; Ebner D; Tracey I; Serra J; Bennett DL
Neuron; 2019 Mar; 101(5):905-919.e8. PubMed ID: 30795902
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Loss of Prdm12 during development, but not in mature nociceptors, causes defects in pain sensation.
Landy MA; Goyal M; Casey KM; Liu C; Lai HC
Cell Rep; 2021 Mar; 34(13):108913. PubMed ID: 33789102
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Molecular genetic analysis in 21 Chinese families with congenital insensitivity to pain with or without anhidrosis.
Zhao F; Mao B; Geng X; Ren X; Wang Y; Guan Y; Li S; Li L; Zhang S; You Y; Cao Y; Yang T; Zhao X
Eur J Neurol; 2020 Aug; 27(8):1697-1705. PubMed ID: 32219930
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. [Congenital insensitivity to pain].
Danziger N; Willer JC
Rev Neurol (Paris); 2009 Feb; 165(2):129-36. PubMed ID: 18808773
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Structural analysis of TrkA mutations in patients with congenital insensitivity to pain reveals PLCγ as an analgesic drug target.
Moraes BC; Ribeiro-Filho HV; Roldão AP; Toniolo EF; Carretero GPB; Sgro GG; Batista FAH; Berardi DE; Oliveira VRS; Tomasin R; Vieceli FM; Pramio DT; Cardoso AB; Figueira ACM; Farah SC; Devi LA; Dale CS; de Oliveira PSL; Schechtman D
Sci Signal; 2022 Apr; 15(731):eabm6046. PubMed ID: 35471943
[TBL] [Abstract][Full Text] [Related]
16. Understanding pain perception through genetic painlessness diseases: The role of NGF and proNGF.
Testa G; Cattaneo A; Capsoni S
Pharmacol Res; 2021 Jul; 169():105662. PubMed ID: 34000361
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Pharmacological characterization of a rat Nav1.7 loss-of-function model with insensitivity to pain.
Chen L; Effraim PR; Carrara J; Zhao P; Dib-Hajj FB; Dib-Hajj SD; Waxman SG
Pain; 2020 Jun; 161(6):1350-1360. PubMed ID: 31977939
[TBL] [Abstract][Full Text] [Related]
20. Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9.
Phatarakijnirund V; Mumm S; McAlister WH; Novack DV; Wenkert D; Clements KL; Whyte MP
Bone; 2016 Mar; 84():289-298. PubMed ID: 26746779
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
