175 related articles for article (PubMed ID: 7924091)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Sensory neuropathy in infantile onset spinocerebellar ataxia (IOSCA).
Koskinen T; Sainio K; Rapola J; Pihko H; Paetau A
Muscle Nerve; 1994 May; 17(5):509-15. PubMed ID: 8159181
[TBL] [Abstract][Full Text] [Related]
8. Infantile onset spinocerebellar ataxia with sensory neuropathy: a new inherited disease.
Koskinen T; Santavuori P; Sainio K; Lappi M; Kallio AK; Pihko H
J Neurol Sci; 1994 Jan; 121(1):50-6. PubMed ID: 8133312
[TBL] [Abstract][Full Text] [Related]
9. Late-onset hereditary ataxia with global thermoanalgesia and absence of fungiform papillae on the tongue in a Japanese family.
Fukutake T; Kita K; Sakakibara R; Takagi K; Tokumaru Y; Kojima S; Hattori T; Hirayama K
Brain; 1996 Jun; 119 ( Pt 3)():1011-21. PubMed ID: 8673478
[TBL] [Abstract][Full Text] [Related]
10. An hereditary sensory and autonomic neuropathy transmitted as an X-linked recessive trait.
Jestico JV; Urry PA; Efphimiou J
J Neurol Neurosurg Psychiatry; 1985 Dec; 48(12):1259-64. PubMed ID: 3866836
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Hereditary sensory and autonomic neuropathy type IID caused by an SCN9A mutation.
Yuan J; Matsuura E; Higuchi Y; Hashiguchi A; Nakamura T; Nozuma S; Sakiyama Y; Yoshimura A; Izumo S; Takashima H
Neurology; 2013 Apr; 80(18):1641-9. PubMed ID: 23596073
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [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]
15. [Case of hereditary sensory neuropathy with atypical clinical course].
Sawicka E; Czyzewski K; Drac H
Neurol Neurochir Pol; 1979; 13(5):541-8. PubMed ID: 293503
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Infantile onset spinocerebellar ataxia with sensory neuropathy (IOSCA): neuropathological features.
Lönnqvist T; Paetau A; Nikali K; von Boguslawski K; Pihko H
J Neurol Sci; 1998 Nov; 161(1):57-65. PubMed ID: 9879682
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [A familial case with hereditary pressure-sensitive neuropathy, with "tomacula"--the first case in Japan].
Minauchi Y; Kohka M; Igata A; Ohkatsu Y
Rinsho Shinkeigaku; 1982 Oct; 22(10):918-25. PubMed ID: 6963557
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]