240 related articles for article (PubMed ID: 18808773)
1. [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]
2. Is pain the price of empathy? The perception of others' pain in patients with congenital insensitivity to pain.
Danziger N; Prkachin KM; Willer JC
Brain; 2006 Sep; 129(Pt 9):2494-507. PubMed ID: 16799175
[TBL] [Abstract][Full Text] [Related]
3. [Pain and analgesia : Mutations of voltage-gated sodium channels].
Eberhardt MJ; Leffler A
Schmerz; 2017 Feb; 31(1):14-22. PubMed ID: 27402262
[TBL] [Abstract][Full Text] [Related]
4. [Hereditary sensory and autonomic neuropathies. The neurophysiological and pathological aspects of two cases with congenital insensitivity to pain].
Esteban-García A; Salinero-Paniagua E; Traba A; Prieto-Montalvo J; Polo-Arrondo AP; Godes-Medrano B; Fernández-Lorente J
Rev Neurol; 2004 Sep 16-30; 39(6):525-9. PubMed ID: 15467989
[TBL] [Abstract][Full Text] [Related]
5. Haploinsufficiency of the nerve growth factor beta gene in a 1p13 deleted female child with an insensitivity to pain.
Fitzgibbon GJ; Kingston H; Needham M; Gaunt L
Dev Med Child Neurol; 2009 Oct; 51(10):833-7. PubMed ID: 19183217
[TBL] [Abstract][Full Text] [Related]
6. A mutation in the nerve growth factor beta gene (NGFB) causes loss of pain perception.
Einarsdottir E; Carlsson A; Minde J; Toolanen G; Svensson O; Solders G; Holmgren G; Holmberg D; Holmberg M
Hum Mol Genet; 2004 Apr; 13(8):799-805. PubMed ID: 14976160
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Two brothers with a variant of hereditary sensory neuropathy.
Pavone L; Huttenlocher P; Siciliano L; Micali G; Rizzo R; Anastasi M; Maimone D; Woolmann R
Neuropediatrics; 1992 Apr; 23(2):92-5. PubMed ID: 1376446
[TBL] [Abstract][Full Text] [Related]
9. Single-Fiber Recordings of Nociceptive Fibers in Patients With HSAN Type V With Congenital Insensitivity to Pain.
Sagafos D; Kleggetveit IP; Helås T; Schmidt R; Minde J; Namer B; Schmelz M; Jørum E
Clin J Pain; 2016 Jul; 32(7):636-42. PubMed ID: 27270876
[TBL] [Abstract][Full Text] [Related]
10. [Clinical and genetic aspects of congenital insensitivity to pain with anhidrosis].
Schwarzkopf R; Pinsk V; Weisel Y; Atar D; Gorzak Y
Harefuah; 2005 Jun; 144(6):433-7, 453, 452. PubMed ID: 15999564
[TBL] [Abstract][Full Text] [Related]
11. [Sensory and autonomic neuropathies and pain-related channelopathies].
Kurth I
Schmerz; 2015 Aug; 29(4):445-57. PubMed ID: 26219509
[TBL] [Abstract][Full Text] [Related]
12. Dominantly transmitted congenital indifference to pain.
Landrieu P; Said G; Allaire C
Ann Neurol; 1990 May; 27(5):574-8. PubMed ID: 1694419
[TBL] [Abstract][Full Text] [Related]
13. Dorsal root ganglia, sodium channels, and fibromyalgia sympathetic pain.
Martinez-Lavin M; Solano C
Med Hypotheses; 2009 Jan; 72(1):64-6. PubMed ID: 18845401
[TBL] [Abstract][Full Text] [Related]
14. Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.
Indo Y
Hum Mutat; 2001 Dec; 18(6):462-71. PubMed ID: 11748840
[TBL] [Abstract][Full Text] [Related]
15. Tension-type headache as the unique pain experience of a patient with congenital insensitivity to pain.
Danziger N; Willer CJ
Pain; 2005 Oct; 117(3):478-483. PubMed ID: 16154693
[TBL] [Abstract][Full Text] [Related]
16. Congenital insensitivity to pain (hereditary sensory and autonomic neuropathy type V): a rare case report.
Singla S; Marwah N; Dutta S
J Dent Child (Chic); 2008; 75(2):207-11. PubMed ID: 18647521
[TBL] [Abstract][Full Text] [Related]
17. Erythromelalgia: a hereditary pain syndrome enters the molecular era.
Waxman SG; Dib-Hajj SD
Ann Neurol; 2005 Jun; 57(6):785-8. PubMed ID: 15929046
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Congenital insensitivity to pain with anhidrosis: morphological and morphometrical studies on the skin and peripheral nerves.
Itoh Y; Yagishita S; Nakajima S; Nakano T; Kawada H
Neuropediatrics; 1986 May; 17(2):103-10. PubMed ID: 2425284
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]