260 related articles for article (PubMed ID: 28033318)
1. A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies.
Plassais J; Lagoutte L; Correard S; Paradis M; Guaguère E; Hédan B; Pommier A; Botherel N; Cadiergues MC; Pilorge P; Silversides D; Bizot M; Samuels M; Arnan C; Johnson R; Hitte C; Salbert G; Méreau A; Quignon P; Derrien T; André C
PLoS Genet; 2016 Dec; 12(12):e1006482. PubMed ID: 28033318
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Congenital insensitivity to pain: an update.
Nagasako EM; Oaklander AL; Dworkin RH
Pain; 2003 Feb; 101(3):213-219. PubMed ID: 12583863
[No Abstract] [Full Text] [Related]
5. Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiological examinations.
Hilz MJ
Clin Auton Res; 2002 May; 12 Suppl 1():I33-43. PubMed ID: 12102461
[TBL] [Abstract][Full Text] [Related]
6. Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.
Elhennawy K; Reda S; Finke C; Graul-Neumann L; Jost-Brinkmann PG; Bartzela T
J Med Case Rep; 2017 Aug; 11(1):233. PubMed ID: 28807049
[TBL] [Abstract][Full Text] [Related]
7. Canine neuropathies: powerful spontaneous models for human hereditary sensory neuropathies.
Correard S; Plassais J; Lagoutte L; Botherel N; Thibaud JL; Hédan B; Richard L; Lia AS; Delague V; Mège C; Mathis S; Guaguère E; Paradis M; Vallat JM; Quignon P; André C
Hum Genet; 2019 May; 138(5):455-466. PubMed ID: 30955094
[TBL] [Abstract][Full Text] [Related]
8. Hereditary sensory and autonomic neuropathy in a family of mixed breed dogs associated with a novel RETREG1 variant.
Gutierrez-Quintana R; Mellersh C; Wessmann A; Ortega M; Penderis J; Sharpe S; Freeman E; Stevenson L; Burmeister L
J Vet Intern Med; 2021 Sep; 35(5):2306-2314. PubMed ID: 34387380
[TBL] [Abstract][Full Text] [Related]
9. Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies.
Lischka A; Eggermann K; Record CJ; Dohrn MF; Laššuthová P; Kraft F; Begemann M; Dey D; Eggermann T; Beijer D; Šoukalová J; Laura M; Rossor AM; Mazanec R; Van Lent J; Tomaselli PJ; Ungelenk M; Debus KY; Feely SME; Gläser D; Jagadeesh S; Martin M; Govindaraj GM; Singhi P; Baineni R; Biswal N; Ibarra-Ramírez M; Bonduelle M; Gess B; Romero Sánchez J; Suthar R; Udani V; Nalini A; Unnikrishnan G; Marques W; Mercier S; Procaccio V; Bris C; Suresh B; Reddy V; Skorupinska M; Bonello-Palot N; Mochel F; Dahl G; Sasidharan K; Devassikutty FM; Nampoothiri S; Rodovalho Doriqui MJ; Müller-Felber W; Vill K; Haack TB; Dufke A; Abele M; Stucka R; Siddiqi S; Ullah N; Spranger S; Chiabrando D; Bolgül BS; Parman Y; Seeman P; Lampert A; Schulz JB; Wood JN; Cox JJ; Auer-Grumbach M; Timmerman V; de Winter J; Themistocleous AC; Shy M; Bennett DL; Baets J; Hübner CA; Leipold E; Züchner S; Elbracht M; Çakar A; Senderek J; Hornemann T; Woods CG; Reilly MM; Kurth I
Brain; 2023 Dec; 146(12):4880-4890. PubMed ID: 37769650
[TBL] [Abstract][Full Text] [Related]
10. ARL6IP1 mutation causes congenital insensitivity to pain, acromutilation and spastic paraplegia.
Nizon M; Küry S; Péréon Y; Besnard T; Quinquis D; Boisseau P; Marsaud T; Magot A; Mussini JM; Mayrargue E; Barbarot S; Bézieau S; Isidor B
Clin Genet; 2018 Jan; 93(1):169-172. PubMed ID: 28471035
[TBL] [Abstract][Full Text] [Related]
11. Insensitivity to Pain, Self-mutilation, and Neuropathy Associated With PRDM12.
Kaur J; Singanamalla B; Suresh RG; Saini AG
Pediatr Neurol; 2020 Sep; 110():95-96. PubMed ID: 32409124
[No Abstract] [Full Text] [Related]
12. [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]
13. 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]
14. Assessment of the functionality of genome-wide canine SNP arrays and implications for canine disease association studies.
Ke X; Kennedy LJ; Short AD; Seppälä EH; Barnes A; Clements DN; Wood SH; Carter SD; Happ GM; Lohi H; Ollier WE
Anim Genet; 2011 Apr; 42(2):181-90. PubMed ID: 21070295
[TBL] [Abstract][Full Text] [Related]
15. A novel biallelic single base insertion in WNK1 in a Pakistani family with congenital insensitivity to pain.
Pastore S; Harripaul R; Azam M; Vincent JB
J Hum Genet; 2020 May; 65(5):493-496. PubMed ID: 32127623
[TBL] [Abstract][Full Text] [Related]
16. Norrbottnian congenital insensitivity to pain.
Minde JK
Acta Orthop Suppl; 2006 Apr; 77(321):2-32. PubMed ID: 16768023
[TBL] [Abstract][Full Text] [Related]
17. Animal models of chronic pain: their possible validation from human experience with posterior rhizotomy and congenital analgesia (Part I of the second John J. Bonica lecture).
Sweet WH
Pain; 1981 Jun; 10(3):275-295. PubMed ID: 6168994
[No Abstract] [Full Text] [Related]
18. A novel human pain insensitivity disorder caused by a point mutation in ZFHX2.
Habib AM; Matsuyama A; Okorokov AL; Santana-Varela S; Bras JT; Aloisi AM; Emery EC; Bogdanov YD; Follenfant M; Gossage SJ; Gras M; Humphrey J; Kolesnikov A; Le Cann K; Li S; Minett MS; Pereira V; Ponsolles C; Sikandar S; Torres JM; Yamaoka K; Zhao J; Komine Y; Yamamori T; Maniatis N; Panov KI; Houlden H; Ramirez JD; Bennett DLH; Marsili L; Bachiocco V; Wood JN; Cox JJ
Brain; 2018 Feb; 141(2):365-376. PubMed ID: 29253101
[TBL] [Abstract][Full Text] [Related]
19. Acral mutilation and analgesia in 13 French spaniels.
Paradis M; de Jaham C; Page N; Sauve F; Helie P
Vet Dermatol; 2005 Apr; 16(2):87-93. PubMed ID: 15842538
[TBL] [Abstract][Full Text] [Related]
20. Inherited autonomic neuropathies.
Axelrod FB; Hilz MJ
Semin Neurol; 2003 Dec; 23(4):381-90. PubMed ID: 15088259
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]