易患压迫性麻痹的遗传性神经病。电生理和组织病理学方面 - Suppr

Suppr

超能文献

Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects.

作者信息

Behse F, Buchthal F, Carlsen F, Knappeis G G

出版信息

Brain. 1972;95(4):777-94. doi: 10.1093/brain/95.4.777.

DOI:10.1093/brain/95.4.777

PMID:4345910

Abstract

摘要

相似文献

Hereditary neuropathy with liability to pressure palsies. Electrophysiological and histopathological aspects.

Brain. 1972;95(4):777-94. doi: 10.1093/brain/95.4.777.

Recurrent familial neuropathy with liability to pressure palsies: reports of two cases and ultrastructural nerve study.

J Neurol. 1979 Jan 30;220(1):43-55. doi: 10.1007/BF00313147.

Segmental demyelination secondary to axonal degeneration in uremic neuropathy.

Mayo Clin Proc. 1971 Jun;46(6):400-31.

[Familial recurring polytopic neuropathy. A case report].

Nervenarzt. 1982 Oct;53(10):598-602.

Uncompacted myelin in hereditary neuropathy with liability to pressure palsies with the 17 p11.2 deletion.

Folia Neuropathol. 1999;37(4):220-6.

[Hereditary neuropathy with liability to pressure palsies (tomaculous neuropathy). Clinical, electrophysical and molecular study of two affected families].

Rev Neurol. 2000;31(6):506-10.

Tomaculous neuropathy: hereditary predisposition to pressure palsies.

Aust N Z J Med. 1985 Oct;15(5):598-603.

Familial neuropathy with liability to pressure palsies. Report of a case.

Ital J Neurol Sci. 1981 Aug;2(3):229-36. doi: 10.1007/BF02335402.

Hereditary neuropathy with liability to pressure palsies: a clinical, electroneurophysiological and morphological study.

J Neurol Sci. 1993 Jun;116(2):176-84. doi: 10.1016/0022-510x(93)90323-q.

Nerve conduction velocity of small components in human sensory nerves. Studies in normal and diseased nerves.

Eur Neurol. 1977;16(1-6):270-9. doi: 10.1159/000114908.

引用本文的文献

Role of tubulin post-translational modifications in peripheral neuropathy.

Exp Neurol. 2023 Feb;360:114274. doi: 10.1016/j.expneurol.2022.114274. Epub 2022 Nov 13.

Peripheral myelin protein 22 alters membrane architecture.

Sci Adv. 2017 Jul 5;3(7):e1700220. doi: 10.1126/sciadv.1700220. eCollection 2017 Jul.

DTI Study of Cerebral Normal-Appearing White Matter in Hereditary Neuropathy With Liability to Pressure Palsies (HNPP).

Medicine (Baltimore). 2015 Oct;94(43):e1909. doi: 10.1097/MD.0000000000001909.

Does hereditary neuropathy with liability to pressure palsy predispose to schwannomatosis?

J Clin Neurol. 2014 Oct;10(4):371-2. doi: 10.3988/jcn.2014.10.4.371. Epub 2014 Oct 6.

Functional recovery of regenerating motor axons is delayed in mice heterozygously deficient for the myelin protein P(0) gene.

Neurochem Res. 2013 Jun;38(6):1266-77. doi: 10.1007/s11064-013-1030-3. Epub 2013 Apr 7.

Compression and entrapment syndromes.

Can Fam Physician. 1987 Mar;33:681-5.

Charcot-marie-tooth disease: seventeen causative genes.

J Clin Neurol. 2006 Jun;2(2):92-106. doi: 10.3988/jcn.2006.2.2.92. Epub 2006 Jun 20.

PMP22 expression in dermal nerve myelin from patients with CMT1A.

Brain. 2009 Jul;132(Pt 7):1734-40. doi: 10.1093/brain/awp113. Epub 2009 May 15.

Unusual presentation of hereditary neuropathy with liability to pressure palsies.

J Brachial Plex Peripher Nerve Inj. 2008 Jan 24;3:2. doi: 10.1186/1749-7221-3-2.

Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy.

Neuromolecular Med. 2006;8(1-2):159-74. doi: 10.1385/NMM:8:1:159.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验