These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
309 related articles for article (PubMed ID: 23831200)
1. [Hereditary sensory and autonomic neuropathy type II A: early neurological and skeletal findings]. Esmer C; Díaz Zambrano S; Santos Díaz MA; González Huerta LM; Cuevas Covarrubias SA; Bravo Oro A An Pediatr (Barc); 2014 Apr; 80(4):254-8. PubMed ID: 23831200 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. Arthropathy-related pain in a patient with congenital impairment of pain sensation due to hereditary sensory and autonomic neuropathy type II with a rare mutation in the WNK1/HSN2 gene: a case report. Yamada K; Yuan J; Mano T; Takashima H; Shibata M BMC Neurol; 2016 Oct; 16(1):201. PubMed ID: 27765018 [TBL] [Abstract][Full Text] [Related]
4. Hereditary sensory and autonomic neuropathy with autonomic crises: a Turkish variant of familial dysautonomia? Koy A; Freynhagen R; Mayatepek E; Tibussek D J Child Neurol; 2012 Feb; 27(2):191-6. PubMed ID: 22140130 [TBL] [Abstract][Full Text] [Related]
5. Atypical hereditary sensory and autonomic neuropathy type IV with neither mental retardation nor pain insensitivity. Jung CL; Ki CS; Kim BJ; Lee JH; Sung KS; Kim JW; Park YS J Child Neurol; 2013 Dec; 28(12):1668-72. PubMed ID: 23112235 [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. Three cousins with chronic foot ulcers from late-onset hereditary sensory and autonomic neuropathies type 2 (HSAN2). Aghaei S; Pakmanesh K Dermatol Online J; 2006 Feb; 12(2):5. PubMed ID: 16638398 [TBL] [Abstract][Full Text] [Related]
8. The painless eye: Neurotrophic keratitis in a child suffering from hereditary sensory autonomic neuropathy type IV. Sethi A; Ramasubramanian S; Swaminathan M Indian J Ophthalmol; 2020 Oct; 68(10):2270-2272. PubMed ID: 32971688 [TBL] [Abstract][Full Text] [Related]
10. A novel homozygous mutation in the WNK1/HSN2 gene causing hereditary sensory neuropathy type 2. Potulska-Chromik A; Kabzińska D; Lipowska M; Kostera-Pruszczyk A; Kochański A Acta Biochim Pol; 2012; 59(3):413-5. PubMed ID: 22910560 [TBL] [Abstract][Full Text] [Related]
11. Hereditary sensory and autosomal peripheral neuropathy-type IV: case series and review of literature. Ashwin DP; Chandan GD; Jasleen HK; Rajkumar GC; Rudresh KB; Prashanth R Oral Maxillofac Surg; 2015 Jun; 19(2):117-23. PubMed ID: 25744033 [TBL] [Abstract][Full Text] [Related]
12. Oral manifestations of hereditary sensory and autonomic neuropathy type IV. Congenital insensitivity to pain with anhidrosis. Amano A; Akiyama S; Ikeda M; Morisaki I Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 1998 Oct; 86(4):425-31. PubMed ID: 9798226 [TBL] [Abstract][Full Text] [Related]
13. Not 'indifference to pain' but varieties of hereditary sensory and autonomic neuropathy. Dyck PJ; Mellinger JF; Reagan TJ; Horowitz SJ; McDonald JW; Litchy WJ; Daube JR; Fealey RD; Go VL; Kao PC; Brimijoin WS; Lambert EH Brain; 1983 Jun; 106 (Pt 2)():373-90. PubMed ID: 6189547 [TBL] [Abstract][Full Text] [Related]
14. Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3. Kornak U; Mademan I; Schinke M; Voigt M; Krawitz P; Hecht J; Barvencik F; Schinke T; Gießelmann S; Beil FT; Pou-Serradell A; Vílchez JJ; Beetz C; Deconinck T; Timmerman V; Kaether C; De Jonghe P; Hübner CA; Gal A; Amling M; Mundlos S; Baets J; Kurth I Brain; 2014 Mar; 137(Pt 3):683-92. PubMed ID: 24459106 [TBL] [Abstract][Full Text] [Related]
15. [Molecular genetics of inherited neuropathies]. Takashima H Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790 [TBL] [Abstract][Full Text] [Related]
17. Recurrent abdominal pain in hereditary sensory autonomic neuropathy type II (HSAN-II). Alkaissi H; Al-Sibahee E; Baher H; Eggermann K; Al-Abayechi A; Kurth I Rev Neurol (Paris); 2021 Dec; 177(10):1307-1309. PubMed ID: 34229871 [No Abstract] [Full Text] [Related]
18. Hereditary insensitivity to pain with anhidrosis. Berkovitch M; Copeliovitch L; Tauber T; Vaknin Z; Lahat E Pediatr Neurol; 1998 Sep; 19(3):227-9. PubMed ID: 9806143 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. The coexistence of a novel WNK1 variant and a copy number variation causes hereditary sensory and autonomic neuropathy type IIA. Wang JJ; Yu B; Li Z BMC Med Genet; 2019 May; 20(1):91. PubMed ID: 31132985 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]