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.
121 related articles for article (PubMed ID: 30680846)
21. Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy type II. Davar G; Shalish C; Blumenfeld A; Breakefield XO Pain; 1996 Sep; 67(1):135-139. PubMed ID: 8895241 [TBL] [Abstract][Full Text] [Related]
22. Exclusion of serine palmitoyltransferase long chain base subunit 2 (SPTLC2) as a common cause for hereditary sensory neuropathy. Dawkins JL; Brahmbhatt S; Auer-Grumbach M; Wagner K; Hartung HP; Verhoeven K; Timmerman V; De Jonghe P; Kennerson M; LeGuern E; Nicholson GA Neuromuscul Disord; 2002 Oct; 12(7-8):656-8. PubMed ID: 12207934 [TBL] [Abstract][Full Text] [Related]
23. Hereditary sensory and autonomic neuropathies. Auer-Grumbach M Handb Clin Neurol; 2013; 115():893-906. PubMed ID: 23931820 [TBL] [Abstract][Full Text] [Related]
24. SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I. Verhoeven K; Coen K; De Vriendt E; Jacobs A; Van Gerwen V; Smouts I; Pou-Serradell A; Martin JJ; Timmerman V; De Jonghe P Neurology; 2004 Mar; 62(6):1001-2. PubMed ID: 15037712 [TBL] [Abstract][Full Text] [Related]
25. Ulcero-mutilating neuropathy in an Austrian kinship without linkage to hereditary motor and sensory neuropathy IIB and hereditary sensory neuropathy I loci. Auer-Grumbach M; Wagner K; Timmerman V; De Jonghe P; Hartung HP Neurology; 2000 Jan; 54(1):45-52. PubMed ID: 10636124 [TBL] [Abstract][Full Text] [Related]
26. Hereditary sensory and autonomic neuropathy type IC accompanied by upper motor neuron abnormalities and type II juxtafoveal retinal telangiectasias. Triplett J; Nicholson G; Sue C; Hornemann T; Yiannikas C J Peripher Nerv Syst; 2019 Jun; 24(2):224-229. PubMed ID: 30866134 [TBL] [Abstract][Full Text] [Related]
27. Genetic heterogeneity of hereditary motor and sensory neuropathy type VI. Ippel EF; Wittebol-Post D; Jennekens FG; Bijlsma JB J Child Neurol; 1995 Nov; 10(6):459-63. PubMed ID: 8576556 [TBL] [Abstract][Full Text] [Related]
28. Clinical and neurophysiologic characterization of an European family with hereditary sensory neuropathy, paroxysmal cough and gastroesophageal reflux. Barros P; Morais H; Santos C; Roriz J; Coutinho P Arq Neuropsiquiatr; 2014 Apr; 72(4):269-72. PubMed ID: 24760089 [TBL] [Abstract][Full Text] [Related]
29. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy. Chance PF Neuromolecular Med; 2006; 8(1-2):159-74. PubMed ID: 16775374 [TBL] [Abstract][Full Text] [Related]
30. 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]
38. A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci. Bellone E; Rodolico C; Toscano A; Di Maria E; Cassandrini D; Pizzuti A; Pigullo S; Mazzeo A; Macaione V; Girlanda P; Vita G; Ajmar F; Mandich P Neuromuscul Disord; 2002 Mar; 12(3):286-91. PubMed ID: 11801401 [TBL] [Abstract][Full Text] [Related]
39. Disease mechanisms in hereditary sensory and autonomic neuropathies. Verpoorten N; De Jonghe P; Timmerman V Neurobiol Dis; 2006 Feb; 21(2):247-55. PubMed ID: 16183296 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]