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Infantile neuroaxonal dystrophy.

作者信息

Crome L, Weller S D

出版信息

Arch Dis Child. 1965 Oct;40(213):502-7. doi: 10.1136/adc.40.213.502.

DOI:10.1136/adc.40.213.502
PMID:5829994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2019456/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/8088cc77d0f8/archdisch01578-0053-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/159c0ec552c0/archdisch01578-0052-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/f0ed0b588baa/archdisch01578-0052-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/b6d1be971957/archdisch01578-0052-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/4d0d014a4d04/archdisch01578-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/8088cc77d0f8/archdisch01578-0053-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/159c0ec552c0/archdisch01578-0052-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/f0ed0b588baa/archdisch01578-0052-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/b6d1be971957/archdisch01578-0052-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/4d0d014a4d04/archdisch01578-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df28/2019456/8088cc77d0f8/archdisch01578-0053-b.jpg

相似文献

1
Infantile neuroaxonal dystrophy.婴儿神经轴索性营养不良
Arch Dis Child. 1965 Oct;40(213):502-7. doi: 10.1136/adc.40.213.502.
2
Hallervorden-Spatz disease. Late infantile and adult types, report of two cases.哈勒沃登-施帕茨病。晚发型婴儿型和成人型，两例报告。
Acta Neuropathol. 1968 Jan 2;10(1):1-16. doi: 10.1007/BF00690505.
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
[MRI as an aid for diagnosis of infantile neuroaxonal dystrophy].[磁共振成像辅助诊断婴儿神经轴索性营养不良]
No To Hattatsu. 1992 Sep;24(5):491-3.
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Neuroaxonal dystrophy: its relation to age and central nervous system lesions.神经轴突营养不良：其与年龄及中枢神经系统病变的关系。
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引用本文的文献

1
[Clinical features of infantile neuroaxonal dystrophy and PLA2G6 gene testing].[婴儿神经轴索性营养不良的临床特征及PLA2G6基因检测]
Zhongguo Dang Dai Er Ke Za Zhi. 2019 Sep;21(9):851-855. doi: 10.7499/j.issn.1008-8830.2019.09.002.
2
[Infantile neuroaxonal dystrophy. Early form with preferential cerebellar involvement].
Acta Neuropathol. 1968 Mar 4;10(2):123-31. doi: 10.1007/BF00691306.
3
Neuroaxonal dystrophy. A case of delayed onset and protracted course.
Acta Neuropathol. 1971;17(4):331-40. doi: 10.1007/BF00685019.
4

本文引用的文献

1
NEUROAXONAL DYSTROPHY IN MUCOVISCIDOSIS.黏多糖贮积症中的神经轴索性营养不良
J Neuropathol Exp Neurol. 1964 Oct;23:567-83. doi: 10.1097/00005072-196410000-00001.
2
Infantile neuroaxonal dystrophy.婴儿神经轴索性营养不良
J Neuropathol Exp Neurol. 1963 Apr;22:175-236. doi: 10.1097/00005072-196304000-00001.
3
[Late infantile form of Hallervorden-Spatz disease. II. Histochemical findings; discussion on nosology].
Dtsch Z Nervenheilkd. 1957;176(1):104-25.
[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.
5
An analysis of the ultrastructural findings in infantile neuroaxonal dystrophy (Seitelberger's disease).婴儿神经轴索性营养不良（塞特尔贝格尔病）的超微结构研究结果分析。
Acta Neuropathol. 1974 Mar 26;27(3):201-13. doi: 10.1007/BF00687630.
6
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.
7
Infantile neuroaxonal dystrophy. Histological and electron microscopical study of two cases.
Acta Neuropathol. 1974;29(2):115-26. doi: 10.1007/BF00684770.
8
[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]
Z Neurol. 1972;201(2):160-95.