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.
138 related articles for article (PubMed ID: 10025138)
1. [Monozygotic twins with suspected hereditary sensory and autonomic neuropathy (HSAN) type V]. Itoh Y; Shishikura K; Suzuki H; Hirano K; Funatsuka M; Hirano Y; Imaizumi T; Awaya Y; Osawa M No To Hattatsu; 1999 Jan; 31(1):63-9. PubMed ID: 10025138 [TBL] [Abstract][Full Text] [Related]
2. Terminal changes in hereditary sensory and autonomic neuropathy: a long-term follow-up of a sporadic case. Lee SS; Lee SH; Han SH Clin Neurol Neurosurg; 2003 Jul; 105(3):175-9. PubMed ID: 12860510 [TBL] [Abstract][Full Text] [Related]
3. [A case of hereditary sensory autonomic neuropathy type II with late onset]. Shimoya K; Ishimoto S; Ohnishi A; Yamamoto T Rinsho Shinkeigaku; 1999 May; 39(5):551-4. PubMed ID: 10424148 [TBL] [Abstract][Full Text] [Related]
4. A case of hereditary sensory and autonomic neuropathy (HSAN) type II. Alibhoy AT; Senanayake B; Fernando MA; Ranawaka UK; Wijesekera JC Ceylon Med J; 2000 Mar; 45(1):32-3. PubMed ID: 11006618 [TBL] [Abstract][Full Text] [Related]
5. No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V. Toscano E; Simonati A; Indo Y; Andria G Ann Neurol; 2002 Aug; 52(2):224-7. PubMed ID: 12210794 [TBL] [Abstract][Full Text] [Related]
6. Painless fractures and thermoregulation disturbances in sensory-autonomic neuropathy: electrophysiological abnormalities and sural nerve biopsy. Polo A; Aldegheri R; Bongiovanni LG; Cavallaro T; Rizzuto N Neuropediatrics; 2000 Jun; 31(3):148-50. PubMed ID: 10963103 [TBL] [Abstract][Full Text] [Related]
7. Hereditary sensory and autonomic neuropathy type I in a Chinese family: British C133W mutation exists in the Chinese. Bi H; Gao Y; Yao S; Dong M; Headley AP; Yuan Y Neuropathology; 2007 Oct; 27(5):429-33. PubMed ID: 18018475 [TBL] [Abstract][Full Text] [Related]
8. Hereditary sensory neuropathy: biopsy study of an autosomal dominant variety. Danon MJ; Carpenter S Neurology; 1985 Aug; 35(8):1226-9. PubMed ID: 3860748 [TBL] [Abstract][Full Text] [Related]
9. Hereditary sensory and autonomic neuropathy with ataxia and late onset. Marbini A; Pavesi G; Cenacchi G; Mazzucchi A; Preda P; Gemignani F Clin Neurol Neurosurg; 1994 May; 96(2):191-6. PubMed ID: 7924091 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. The clinical spectrum and morphology of type II hereditary sensory neuropathy. Nukada H; Pollock M; Haas LF Brain; 1982 Dec; 105 (Pt 4)():647-65. PubMed ID: 6958343 [TBL] [Abstract][Full Text] [Related]
12. Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I). Houlden H; King R; Blake J; Groves M; Love S; Woodward C; Hammans S; Nicoll J; Lennox G; O'Donovan DG; Gabriel C; Thomas PK; Reilly MM Brain; 2006 Feb; 129(Pt 2):411-25. PubMed ID: 16364956 [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. Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensation. Guven Y; Altunoglu U; Aktoren O; Uyguner ZO; Kayserili H; Kaewkahya M; Kantaputra PN Eur J Med Genet; 2014 Apr; 57(5):240-6. PubMed ID: 24631696 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Familial sensory autonomic neuropathy with arthropathy in Navajo children. Johnsen SD; Johnson PC; Stein SR Neurology; 1993 Jun; 43(6):1120-5. PubMed ID: 8170555 [TBL] [Abstract][Full Text] [Related]
18. Hereditary sensory neuropathy with neurotrophic keratitis. Description of an autosomal recessive disorder with a selective reduction of small myelinated nerve fibres and a discussion of the classification of the hereditary sensory neuropathies. Donaghy M; Hakin RN; Bamford JM; Garner A; Kirkby GR; Noble BA; Tazir-Melboucy M; King RH; Thomas PK Brain; 1987 Jun; 110 ( Pt 3)():563-83. PubMed ID: 3472625 [TBL] [Abstract][Full Text] [Related]
19. Congenital sensory neuropathy with selective loss of small myelinated fibers. Low PA; Burke WJ; McLeod JG Ann Neurol; 1978 Feb; 3(2):179-82. PubMed ID: 77656 [TBL] [Abstract][Full Text] [Related]
20. A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V. Houlden H; King RH; Hashemi-Nejad A; Wood NW; Mathias CJ; Reilly M; Thomas PK Ann Neurol; 2001 Apr; 49(4):521-5. PubMed ID: 11310631 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]