270 related articles for article (PubMed ID: 26746779)
21. 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]
22. Painful and painless channelopathies.
Bennett DL; Woods CG
Lancet Neurol; 2014 Jun; 13(6):587-99. PubMed ID: 24813307
[TBL] [Abstract][Full Text] [Related]
23. Congenital insensitivity to pain with anhidrosis (CIPA): the spectrum of radiological findings.
Schulman H; Tsodikow V; Einhorn M; Levy Y; Shorer Z; Hertzanu Y
Pediatr Radiol; 2001 Oct; 31(10):701-5. PubMed ID: 11685437
[TBL] [Abstract][Full Text] [Related]
24. Congenital insensitivity to pain in one family.
Svec A; Feldinszka J; Kokavec M
J Pediatr Orthop B; 2018 Jul; 27(4):369-374. PubMed ID: 27941533
[TBL] [Abstract][Full Text] [Related]
25. Case Report: Mutant
Xie XH; Tang JG; Liu ZH; Peng SJ; Yuan ZZ; Gu H; Hu YQ; Tan ZP
Front Neurosci; 2021; 15():697167. PubMed ID: 34335171
[TBL] [Abstract][Full Text] [Related]
26. The phenotype of congenital insensitivity to pain due to the NaV1.9 variant p.L811P.
Woods CG; Babiker MO; Horrocks I; Tolmie J; Kurth I
Eur J Hum Genet; 2015 May; 23(5):561-3. PubMed ID: 25118027
[No Abstract] [Full Text] [Related]
27. Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant.
Leipold E; Hanson-Kahn A; Frick M; Gong P; Bernstein JA; Voigt M; Katona I; Oliver Goral R; Altmüller J; Nürnberg P; Weis J; Hübner CA; Heinemann SH; Kurth I
Nat Commun; 2015 Dec; 6():10049. PubMed ID: 26645915
[TBL] [Abstract][Full Text] [Related]
28. Alcohol-aggravated episodic pain in humans with SCN11A mutation and ALDH2 polymorphism.
Yang L; Li L; Tang H; Ma T; Li Y; Zhang X; Shi X; Liu JY
Pain; 2020 Jul; 161(7):1470-1482. PubMed ID: 32132394
[TBL] [Abstract][Full Text] [Related]
29. Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7).
Whyte MP; Campeau PM; McAlister WH; Roodman GD; Kurihara N; Nenninger A; Duan S; Gottesman GS; Bijanki VN; Sedighi H; Veis DJ; Mumm S
Bone; 2020 Aug; 137():115364. PubMed ID: 32298837
[TBL] [Abstract][Full Text] [Related]
30. [Paroxysmal limb intolerable pain (infantile pain episodes associated with novel Nav1.9 mutations in familial episodic pain syndrome)].
Noguchi A; Takahashi T; Okuda H; Kobayashi H; Koizumi A
Nihon Rinsho; 2017 Apr; 75(4):641-651. PubMed ID: 30549873
[TBL] [Abstract][Full Text] [Related]
31. A de novo gain-of-function mutation in SCN11A causes loss of pain perception.
Leipold E; Liebmann L; Korenke GC; Heinrich T; Giesselmann S; Baets J; Ebbinghaus M; Goral RO; Stödberg T; Hennings JC; Bergmann M; Altmüller J; Thiele H; Wetzel A; Nürnberg P; Timmerman V; De Jonghe P; Blum R; Schaible HG; Weis J; Heinemann SH; Hübner CA; Kurth I
Nat Genet; 2013 Nov; 45(11):1399-404. PubMed ID: 24036948
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. 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]
34. 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]
35. 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]
36. 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]
37. [Osteoarticular lesions in pain perception deficit disorders in children].
Fauré C; Sagui M
J Radiol; 1983 Dec; 64(12):667-74. PubMed ID: 6198516
[TBL] [Abstract][Full Text] [Related]
38. Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation.
Rickels MR; Zhang X; Mumm S; Whyte MP
J Bone Miner Res; 2005 May; 20(5):878-85. PubMed ID: 15824861
[TBL] [Abstract][Full Text] [Related]
39. Gain-of-function mutation p.Arg225Cys in SCN11A causes familial episodic pain and contributes to essential tremor.
Leng XR; Qi XH; Zhou YT; Wang YP
J Hum Genet; 2017 Jun; 62(6):641-646. PubMed ID: 28298626
[TBL] [Abstract][Full Text] [Related]
40. Familial episodic limb pain in kindreds with novel Nav1.9 mutations.
Kabata R; Okuda H; Noguchi A; Kondo D; Fujiwara M; Hata K; Kato Y; Ishikawa K; Tanaka M; Sekine Y; Hishikawa N; Mizukami T; Ito J; Akasaka M; Sakurai K; Yoshida T; Minoura H; Hayashi T; Inoshita K; Matsuyama M; Kinjo N; Cao Y; Inoue S; Kobayashi H; Harada KH; Youssefian S; Takahashi T; Koizumi A
PLoS One; 2018; 13(12):e0208516. PubMed ID: 30557356
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
