172 related articles for article (PubMed ID: 19593630)
1. Developments in autonomic research: a review of the latest literature.
Macefield VG
Clin Auton Res; 2009 Aug; 19(4):193-6. PubMed ID: 19593630
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [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]
5. Neurobiology of pain, interoception and emotional response: lessons from nerve growth factor-dependent neurons.
Indo Y
Eur J Neurosci; 2014 Feb; 39(3):375-91. PubMed ID: 24494678
[TBL] [Abstract][Full Text] [Related]
6. Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis.
Indo Y
Clin Genet; 2012 Oct; 82(4):341-50. PubMed ID: 22882139
[TBL] [Abstract][Full Text] [Related]
7. Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor.
Indo Y
Clin Auton Res; 2002 May; 12 Suppl 1():I20-32. PubMed ID: 12102460
[TBL] [Abstract][Full Text] [Related]
8. In vitro receptor binding properties of a "painless" NGF mutein, linked to hereditary sensory autonomic neuropathy type V.
Covaceuszach S; Capsoni S; Marinelli S; Pavone F; Ceci M; Ugolini G; Vignone D; Amato G; Paoletti F; Lamba D; Cattaneo A
Biochem Biophys Res Commun; 2010 Jan; 391(1):824-9. PubMed ID: 19945432
[TBL] [Abstract][Full Text] [Related]
9. Nerve growth factor, pain, itch and inflammation: lessons from congenital insensitivity to pain with anhidrosis.
Indo Y
Expert Rev Neurother; 2010 Nov; 10(11):1707-24. PubMed ID: 20977328
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
14. Mutations in sodium-channel gene SCN9A cause a spectrum of human genetic pain disorders.
Drenth JP; Waxman SG
J Clin Invest; 2007 Dec; 117(12):3603-9. PubMed ID: 18060017
[TBL] [Abstract][Full Text] [Related]
15. Nerve growth factor, interoception, and sympathetic neuron: lesson from congenital insensitivity to pain with anhidrosis.
Indo Y
Auton Neurosci; 2009 May; 147(1-2):3-8. PubMed ID: 19201660
[TBL] [Abstract][Full Text] [Related]
16. Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.
Altassan R; Saud HA; Masoodi TA; Dosssari HA; Khalifa O; Al-Zaidan H; Sakati N; Rhabeeni Z; Al-Hassnan Z; Binamer Y; Alhashemi N; Wade W; Al-Zayed Z; Al-Sayed M; Al-Muhaizea MA; Meyer B; Al-Owain M; Wakil SM
Am J Med Genet A; 2017 Apr; 173(4):1009-1016. PubMed ID: 28328124
[TBL] [Abstract][Full Text] [Related]
17. Whole exome sequencing in congenital pain insensitivity identifies a novel causative intronic NTRK1-mutation due to uniparental disomy.
Kurth I; Baumgartner M; Schabhüttl M; Tomni C; Windhager R; Strom TM; Wieland T; Gremel K; Auer-Grumbach M
Am J Med Genet B Neuropsychiatr Genet; 2016 Sep; 171(6):875-8. PubMed ID: 27184211
[TBL] [Abstract][Full Text] [Related]
18. Insensitivity to Pain upon Adult-Onset Deletion of Nav1.7 or Its Blockade with Selective Inhibitors.
Shields SD; Deng L; Reese RM; Dourado M; Tao J; Foreman O; Chang JH; Hackos DH
J Neurosci; 2018 Nov; 38(47):10180-10201. PubMed ID: 30301756
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. 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]
[Next] [New Search]
