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Items: 1 to 20 of 183

1.

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 30;80(18):1641-9. doi: 10.1212/WNL.0b013e3182904fdd.

PMID:
23596073
2.

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.

PMID:
18018475
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.

PMID:
1376446
5.

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.

PMID:
11310631
6.

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.

PMID:
12860510
7.

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.

PMID:
7924091
8.

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.

PMID:
16364956
9.

Hereditary sensory neuropathy: biopsy study of an autosomal dominant variety.

Danon MJ, Carpenter S.

Neurology. 1985 Aug;35(8):1226-9.

PMID:
3860748
10.

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.

PMID:
10963103
11.

The evaluation of autonomic nervous function in a patient with hereditary sensory and autonomic neuropathy type IV with novel mutations of the TRKA gene.

Ohto T, Iwasaki N, Fujiwara J, Ohkoshi N, Kimura S, Kawade K, Tanaka R, Matsui A.

Neuropediatrics. 2004 Oct;35(5):274-8.

PMID:
15534759
13.

Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE.

Yuan J, Higuchi Y, Nagado T, Nozuma S, Nakamura T, Matsuura E, Hashiguchi A, Sakiyama Y, Yoshimura A, Takashima H.

J Peripher Nerv Syst. 2013 Mar;18(1):89-93. doi: 10.1111/jns5.12012.

PMID:
23521649
14.

[Molecular genetics of inherited neuropathies].

Takashima H.

Rinsho Shinkeigaku. 2006 Jan;46(1):1-18. Review. Japanese.

PMID:
16541790
15.

[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. Japanese.

PMID:
10424148
16.

Autosomal dominant burning feet syndrome.

Stögbauer F, Young P, Kuhlenbäumer G, Kiefer R, Timmerman V, Ringelstein EB, Wang JF, Schröder JM, Van Broeckhoven C, Weis J.

J Neurol Neurosurg Psychiatry. 1999 Jul;67(1):78-81.

17.
18.

Hereditary sensory neuropathy type 1 in a Portuguese family-electrodiagnostic and autonomic nervous system studies.

Geraldes R, de Carvalho M, Santos-Bento M, Nicholson G.

J Neurol Sci. 2004 Dec 15;227(1):35-8.

PMID:
15546589

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