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肌萎缩侧索硬化症中的异位神经元。

Heterotopic neurons in amyotrophic lateral sclerosis.

作者信息

Martin J E, Mather K, Swash M

机构信息

Department of Neuropathology, Royal London Hospital, Whitechapel, UK.

出版信息

Neurology. 1993 Jul;43(7):1420-2. doi: 10.1212/wnl.43.7.1420.

DOI:10.1212/wnl.43.7.1420
PMID:8327148
Abstract

Heterotopic neurons in ALS have suggested aberrant neuronal migration during development. We studied 10 cases with ALS, 10 normal controls, and 10 cases with anterior horn cell disease, including spinal muscular atrophy and acute and remote poliomyelitis. There was no excess of heterotopic neurons in ALS compared with either control group and therefore no failure of neuronal migration in ALS.

摘要

肌萎缩侧索硬化症(ALS)中的异位神经元提示其在发育过程中存在异常的神经元迁移。我们研究了10例ALS患者、10例正常对照以及10例前角细胞疾病患者,包括脊髓性肌萎缩症、急性和陈旧性脊髓灰质炎。与任一对照组相比,ALS患者中异位神经元并无增多,因此ALS不存在神经元迁移失败的情况。

相似文献

1
Heterotopic neurons in amyotrophic lateral sclerosis.肌萎缩侧索硬化症中的异位神经元。
Neurology. 1993 Jul;43(7):1420-2. doi: 10.1212/wnl.43.7.1420.
2
Heterotopic neurons in spinal cord of patients with ALS.
Neurology. 1989 May;39(5):644-8. doi: 10.1212/wnl.39.5.644.
3
Autonomic neurons of the sacral spinal cord in amyotrophic lateral sclerosis, anterior poliomyelitis and "neuronal intranuclear hyaline inclusion disease": distribution of sacral autonomic neurons.肌萎缩侧索硬化症、脊髓灰质炎和“神经元核内透明包涵体病”中骶脊髓的自主神经元:骶自主神经元的分布
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4
Characterizations of heterotopic neurons in the spinal cord of amyotrophic lateral sclerosis patients.
Acta Neuropathol. 1998 Apr;95(4):367-72. doi: 10.1007/s004010050812.
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[Spinal pathology in spinal muscular atrophy in comparison with amyotrophic lateral sclerosis].[与肌萎缩侧索硬化症相比,脊髓性肌萎缩症中的脊髓病理学]
Wien Med Wochenschr. 1996;146(9-10):199-200.
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Evidence for sequential degeneration of the neurons in the intermediate zone of the spinal cord in amyotrophic lateral sclerosis: a topographic and quantitative investigation.
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Peripheral nerve involvement in Werdnig-Hoffmann disease.韦尼克-霍夫曼病中的周围神经受累
Brain Dev. 1989;11(4):221-9. doi: 10.1016/s0387-7604(89)80040-3.
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TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.肌萎缩侧索硬化症和脊髓性肌萎缩症小鼠模型中的TDP-43表达
BMC Neurosci. 2008 Oct 28;9:104. doi: 10.1186/1471-2202-9-104.
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Amyotrophic lateral sclerosis.肌萎缩侧索硬化症
AMA Arch Neurol Psychiatry. 1953 Feb;69(2):171-92. doi: 10.1001/archneurpsyc.1953.02320260029002.
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Comparative immunohistochemical study on synaptophysin expression in the anterior horn of post-poliomyelitis and sporadic amyotrophic lateral sclerosis.脊髓灰质炎后和散发性肌萎缩侧索硬化症前角中突触素表达的比较免疫组织化学研究
Acta Neuropathol. 1996 Nov;92(5):473-8. doi: 10.1007/s004010050549.

引用本文的文献

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Demonstration of neurofibrillary tangles and neuropil thread-like structures in spinal cord white matter in parkinsonism-dementia complex on Guam and in Guamanian amyotrophic lateral sclerosis.关岛帕金森病痴呆综合征及关岛肌萎缩侧索硬化症患者脊髓白质中神经原纤维缠结和神经毡线样结构的显示
Acta Neuropathol. 1994;88(2):180-4. doi: 10.1007/BF00294512.