X连锁型夏科-马里-图斯病患者的中枢神经系统炎性脱髓鞘疾病：对那他珠单抗的阳性反应 - Suppr

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超能文献

Inflammatory demyelinating CNS disorder in a case of X-linked Charcot-Marie-Tooth disease: positive response to natalizumab.

作者信息

Weishaupt Jochen H, Ganser Claudia, Bähr Mathias

出版信息

J Neurol. 2012 Sep;259(9):1967-9. doi: 10.1007/s00415-012-6467-9. Epub 2012 Mar 13.

DOI:10.1007/s00415-012-6467-9

PMID:22411047

Abstract

摘要

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Inherited neuropathies: an update.遗传性神经病变：最新进展。

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本文引用的文献

Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects.连接蛋白32突变导致雪旺细胞和少突胶质细胞功能丧失，进而引起周围神经系统和中枢神经系统的髓鞘形成缺陷。

J Neurosci. 2009 Apr 15;29(15):4736-49. doi: 10.1523/JNEUROSCI.0325-09.2009.

X-linked Charcot-Marie-Tooth disease and multiple sclerosis.X连锁型夏科-马里-图斯病与多发性硬化症。

J Neurol. 2007 Jul;254(7):953-5. doi: 10.1007/s00415-006-0324-7. Epub 2007 Jan 30.

Molecular genetics of X-linked Charcot-Marie-Tooth disease.X连锁型夏科-马里-图斯病的分子遗传学

Neuromolecular Med. 2006;8(1-2):107-22. doi: 10.1385/nmm:8:1-2:107.

X-linked Charcot-Marie-Tooth disease and progressive-relapsing central demyelinating disease.X连锁型夏科-马里-图思病与进行性复发型中枢性脱髓鞘疾病

Neurology. 2005 Nov 22;65(10):1672-3. doi: 10.1212/01.wnl.0000186032.06791.94.

Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generations.两代人中患有累及中枢神经系统的1A型夏科-马里-图思病。

J Neurol. 2004 Apr;251(4):484-5. doi: 10.1007/s00415-004-0376-5.

The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem.X连锁型夏科-马里-图斯病的中枢神经系统表型：不止是外周问题。

Neurology. 2003 Dec 9;61(11):1475-8. doi: 10.1212/01.wnl.0000095960.48964.25.

Coexistent hereditary and inflammatory neuropathy.并存的遗传性和炎性神经病。

Brain. 2004 Jan;127(Pt 1):193-202. doi: 10.1093/brain/awh017. Epub 2003 Nov 7.

Demyelinating neuropathies.脱髓鞘性神经病

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