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Evidence of axonal damage in human acute demyelinating diseases.

作者信息

Ghosh N, DeLuca G C, Esiri M M

机构信息

Department of Clinical Neurology, University of Oxford, UK.

出版信息

J Neurol Sci. 2004 Jul 15;222(1-2):29-34. doi: 10.1016/j.jns.2004.03.032.

Abstract

UNLABELLED

Substantial axon damage, detected by immunostaining for beta amyloid precursor protein (betaAPP) has been demonstrated in acute demyelinating lesions in multiple sclerosis.

AIMS

The present study aimed to determine if this was also the case in the other human acute demyelinating diseases, acute hemorrhagic leucoencephalitis (AHLE), acute disseminated encephalomyelitis (ADEM) and central pontine myelinolysis (CPM).

METHODS

BetaAPP immunostaining was used as a marker of axonal damage in autopsy material from these conditions.

RESULTS

Axonal damage was detected in all these conditions. Its extent varied within and between them. Axonal damage was largely confined to tissue adjacent to veins and venules in AHLE and ADEM but was unrelated to proximity to these vessels in CPM.

CONCLUSION

Substantial axon damage occurs in fatal cases of AHLE, ADEM and CPM.

摘要

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