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Infantile neuroaxonal dystrophy. Clinical, pathologic, and histochemical findings in a family with 3 affected siblings.

作者信息

Huttenlocher P R, Gilles F H

出版信息

Neurology. 1967 Dec;17(12):1174-84. doi: 10.1212/wnl.17.12.1174.

DOI:10.1212/wnl.17.12.1174
PMID:6070019
Abstract
摘要

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引用本文的文献

1
New enzymatic findings in infantile neuroaxonal dystrophy.婴儿神经轴索性营养不良的新酶学发现。
Acta Neuropathol. 1983;60(1-2):153-5. doi: 10.1007/BF00685362.
2
Neuroaxonal dystrophy. A case of delayed onset and protracted course.
Acta Neuropathol. 1971;17(4):331-40. doi: 10.1007/BF00685019.
3
[Infantile neuroaxomal dystrophy or Seitelberger's disease. Clinical, histological and ultrastructural study of 2 observations].
Acta Neuropathol. 1970;15(4):327-50. doi: 10.1007/BF00684731.
4
Neuroaxonal dystrophy. A case of non pigmented type and protracted course.
Acta Neuropathol. 1972;21(3):232-8. doi: 10.1007/BF00688502.
5
Giant axonal neuropathy--a unique case with segmental neurofilamentous masses.巨大轴索性神经病——一例伴有节段性神经丝团块的独特病例。
Acta Neuropathol. 1972;20(3):237-47. doi: 10.1007/BF00686905.
6
Electron microscopic study on schizophrenia. Mechanism of pathological changes.精神分裂症的电子显微镜研究。病理变化机制。
Acta Neuropathol. 1972;20(1):67-77. doi: 10.1007/BF00687903.
7
Feline hereditary neuroaxonal dystrophy.猫遗传性神经轴索性营养不良
Am J Pathol. 1974 Mar;74(3):551-66.
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[A contribution concerning the infantile neuro-axonal dystrophy. Comparison to Hallervorden-Spatz disease regarding histopathologic findings and clinical symptoms].[关于婴儿神经轴索性营养不良的一项研究。在组织病理学发现和临床症状方面与苍白球黑质变性的比较]
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