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广泛的核内神经元小体(马里内斯科小体)与一种伴有颅神经和周围神经受累的家族性脊髓变性相关。

Widespread intranuclear neuronal corpuscles (Marinesco bodies) associated with a familial spinal degeneration with cranial and peripheral nerve involvement.

作者信息

Janota I

出版信息

Neuropathol Appl Neurobiol. 1979 Aug;5(4):311-7. doi: 10.1111/j.1365-2990.1979.tb00630.x.

DOI:10.1111/j.1365-2990.1979.tb00630.x
PMID:225694
Abstract

Widespread intranuclear, paranucleolar, acidophilic corpuscles, known as Marinesco bodies, were found in association with degeneration of the posterior columns of ting at the age of 45 years. Neurological examination of his sister (aged 51 years) inciates that she is suffering from the same diseases. The cases appear to belong to the predominantly spinal form of spino-cerebellar degenerations or Friedreich's ataxia. This report, which includes an electron microscope examination, considers the pathological significance of Marinesco bodies.

摘要

在一名45岁男性患者中,发现广泛存在的核内、核仁旁嗜酸性小体,即马里内斯科小体,与脊髓后柱变性有关。对其51岁姐姐的神经学检查表明她也患有同样的疾病。这些病例似乎属于脊髓小脑变性的主要脊髓型或弗里德赖希共济失调。本报告包括电子显微镜检查,探讨了马里内斯科小体的病理意义。

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Widespread intranuclear neuronal corpuscles (Marinesco bodies) associated with a familial spinal degeneration with cranial and peripheral nerve involvement.广泛的核内神经元小体(马里内斯科小体)与一种伴有颅神经和周围神经受累的家族性脊髓变性相关。
Neuropathol Appl Neurobiol. 1979 Aug;5(4):311-7. doi: 10.1111/j.1365-2990.1979.tb00630.x.
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[Mendel type spino-cerebellar degeneration. On the fundamentally spinal cord forms].[孟德尔型脊髓小脑变性。论基本的脊髓型]
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引用本文的文献

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2
George Marinesco in the Constellation of Modern Neuroscience.现代神经科学领域中的乔治·马里内斯科。
Front Neurosci. 2017 Dec 25;11:726. doi: 10.3389/fnins.2017.00726. eCollection 2017.
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Clinicopathological features of adult-onset neuronal intranuclear inclusion disease.成人起病的神经元核内包涵体病的临床病理特征
Brain. 2016 Dec;139(Pt 12):3170-3186. doi: 10.1093/brain/aww249. Epub 2016 Oct 25.
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Neuronal intranuclear inclusion disease without polyglutamine inclusions in a child.一名儿童患无多聚谷氨酰胺包涵体的神经元核内包涵体病。
J Neuropathol Exp Neurol. 2005 Jun;64(6):545-52. doi: 10.1093/jnen/64.6.545.
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Generalised nuclear and cytoplasmic inclusion disease: a rare case investigated by microscopy and immunohistochemistry.
Acta Neuropathol. 1994;87(6):648-54. doi: 10.1007/BF00293327.
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Intranuclear inclusions in muscle, nervous tissue, and adrenal gland.肌肉、神经组织和肾上腺中的核内包涵体。
Acta Neuropathol. 1984;63(1):24-32. doi: 10.1007/BF00688467.
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Multiple system atrophy with neuronal intranuclear hyaline inclusions. Report of a new case with light and electron microscopic studies.伴有神经元核内透明包涵体的多系统萎缩。一例新病例的光镜和电镜研究报告。
Acta Neuropathol. 1981;54(2):113-9. doi: 10.1007/BF00689403.
8
Light, fluorescence, and electron microscopic features of neuronal intranuclear hyaline inclusions associated with multisystem atrophy.与多系统萎缩相关的神经元核内透明包涵体的光镜、荧光镜及电镜特征
Acta Neuropathol. 1980;50(2):115-20. doi: 10.1007/BF00692861.
9
Neuronal intranuclear hyaline inclusion disease in a nine year old.一名9岁儿童的神经元核内透明包涵体病
Acta Neuropathol. 1986;70(3-4):327-32. doi: 10.1007/BF00686092.
10
Neuronal intranuclear hyaline inclusion disease presenting as Friedreich's ataxia.表现为弗里德赖希共济失调的神经元核内透明包涵体病
Acta Neuropathol. 1985;65(3-4):322-9. doi: 10.1007/BF00687016.