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Autonomic dysfunction in Lambert-Eaton myasthenic syndrome.

作者信息

Khurana R K, Koski C L, Mayer R F

机构信息

Department of Neurology, University of Maryland School of Medicine, Baltimore 21201.

出版信息

J Neurol Sci. 1988 May;85(1):77-86. doi: 10.1016/0022-510x(88)90037-8.

DOI:10.1016/0022-510x(88)90037-8
PMID:2838585
Abstract

Autonomic symptoms were observed in 6 patients with clinically and electrophysiologically documented Lambert-Eaton myasthenic syndrome (LEMS). Of the 6 patients, 2 were extensively investigated in the laboratory. In contrast to previous reports which recognized only cholinergic dysautonomia, abnormalities of sympathetic as well as parasympathetic function were evident. Of the 6 patients, 4 had small cell lung cancer (SCLC). In one male patient, chemotherapy for SCLC resulted in an early improvement of autonomic dysfunction and the electrophysiological defect, documenting simultaneous regression of dysautonomia and LEMS. In addition, the patients with SCLC and LEMS had a survival thus far of 3-13 years suggesting that a subgroup of SCLC patients have a better prognosis.

摘要

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引用本文的文献

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Lambert-Eaton Myasthenic Syndrome.兰伯特-伊顿肌无力综合征
Neurol Clin. 2018 May;36(2):379-394. doi: 10.1016/j.ncl.2018.01.008.
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Ca2+ channels as targets of neurological disease: Lambert-Eaton Syndrome and other Ca2+ channelopathies.作为神经疾病靶点的钙离子通道:兰伯特-伊顿综合征及其他钙离子通道病
J Bioenerg Biomembr. 2003 Dec;35(6):697-718. doi: 10.1023/b:jobb.0000008033.02320.10.
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Passive transfer of Lambert-Eaton syndrome to mice induces dihydropyridine sensitivity of neuromuscular transmission.将兰伯特-伊顿综合征被动转移至小鼠会诱导神经肌肉传递的二氢吡啶敏感性。
J Physiol. 2002 Sep 1;543(Pt 2):567-76. doi: 10.1113/jphysiol.2002.021048.
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Autonomic dysfunction in Lambert-Eaton myasthenic syndrome.兰伯特-伊顿肌无力综合征中的自主神经功能障碍。
Clin Auton Res. 2001 Jun;11(3):145-54. doi: 10.1007/BF02329922.
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Lambert-Eaton myasthenic syndrome.兰伯特-伊顿肌无力综合征
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