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Infantile neuroaxonal dystrophy. A disease characterized by altered terminal axons and synaptic endings.

作者信息

Hedley-Whyte E T, Gilles F H, Uzman B G

出版信息

Neurology. 1968 Sep;18(9):891-906. doi: 10.1212/wnl.18.9.891.

DOI:10.1212/wnl.18.9.891
PMID:4176658
Abstract
摘要

相似文献

1
Infantile neuroaxonal dystrophy. A disease characterized by altered terminal axons and synaptic endings.
Neurology. 1968 Sep;18(9):891-906. doi: 10.1212/wnl.18.9.891.
2
Electron microscopic observations in infantile neuroaxonal dystrophy. Report of a cortical biopsy and review of the recent literature.婴儿神经轴索性营养不良的电子显微镜观察。一例皮质活检报告及近期文献综述。
Arch Neurol. 1969 Jan;20(1):19-34. doi: 10.1001/archneur.1969.00480070029004.
3
Infantile neuroaxonal dystrophy and its relationship to Hallervorden-Spatz disease.
Neurology. 1968 Jul;18(7):693-9. doi: 10.1212/wnl.18.7.693.
4
Aberrant synaptic development.异常的突触发育。
Arch Neurol. 1973 Jun;28(6):359-66. doi: 10.1001/archneur.1973.00490240019001.
5
Infantile neuroaxonal dystrophy. Clinical, pathologic, and histochemical findings in a family with 3 affected siblings.
Neurology. 1967 Dec;17(12):1174-84. doi: 10.1212/wnl.17.12.1174.
6
An electron microscopic study of terminal degeneration in the neocortex of the cat.猫新皮质终末变性的电子显微镜研究。
Philos Trans R Soc Lond B Biol Sci. 1970 Jan 29;257(812):29-43. doi: 10.1098/rstb.1970.0006.
7
Infantile neuroaxonal dystrophy with neonatal onset. Neuropathologic and electron microscopic observations.
J Neuropathol Exp Neurol. 1968 Apr;27(2):300-23. doi: 10.1097/00005072-196804000-00008.
8
[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.
9
Infantile neuroaxonal dystrophy. Neuropathological and biochemical study of a case.婴儿神经轴索性营养不良。1例病例的神经病理学和生化研究。
Arch Neurol. 1972 May;26(5):391-402. doi: 10.1001/archneur.1972.00490110025002.
10
Neuroaxonal dystrophy in a group of related cats.一组相关猫的神经轴突营养不良
J Vet Diagn Invest. 1993 Oct;5(4):585-90. doi: 10.1177/104063879300500414.

引用本文的文献

1
Exploring therapeutic strategies for infantile neuronal axonal dystrophy (INAD/PARK14).探讨婴儿神经元轴突营养不良(INAD/PARK14)的治疗策略。
Elife. 2023 Jan 16;12:e82555. doi: 10.7554/eLife.82555.
2
High expression of α-synuclein in damaged mitochondria with PLA2G6 dysfunction.α-突触核蛋白在 PLA2G6 功能障碍的损伤线粒体中高表达。
Acta Neuropathol Commun. 2016 Mar 30;4:27. doi: 10.1186/s40478-016-0298-3.
3
Morphometric evaluation of primary sensory neurons in experimental p-bromophenylacetylurea intoxication.实验性对溴苯乙酰脲中毒时初级感觉神经元的形态计量学评估
Acta Neuropathol. 1980;52(2):111-8. doi: 10.1007/BF00688008.
4
Morphological alterations of Purkinje cell axons and presynaptic terminals in organotypic cerebellar cultures exposed to ionizing irradiation.暴露于电离辐射的小脑器官型培养物中浦肯野细胞轴突和突触前终末的形态学改变。
Acta Neuropathol. 1981;54(4):301-10. doi: 10.1007/BF00697004.
5
Neuroaxonal dystrophy. A case of delayed onset and protracted course.
Acta Neuropathol. 1971;17(4):331-40. doi: 10.1007/BF00685019.
6
[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.
7
Changes in the central nervous system of lambs following the administration of sodium diethyldithiocarbamate.
Acta Neuropathol. 1970;15(3):197-207. doi: 10.1007/BF00686766.
8
[Infantile neuroaxonal dystrophy or Seitelberger's disease. 3. Ultrastructural study of striated muscle].
Acta Neuropathol. 1971;18(4):327-41. doi: 10.1007/BF00688446.
9
[Neuro-muscular biopsy in the diagnosis of infantile neuroaxonal dystrophy. Ultrastructural study of 3 cases 2 of them familial].[神经肌肉活检在婴儿型神经轴索性营养不良诊断中的应用。3例超微结构研究,其中2例为家族性]
Acta Neuropathol. 1972;21(2):109-16. doi: 10.1007/BF00687565.
10
Profound muscle weakness associated with axis cylinder ballooning. A case report.伴有轴突气球样变的严重肌肉无力。病例报告。
Acta Neuropathol. 1974 May 31;28(1):87-92. doi: 10.1007/BF00687522.