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Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Clinical characteristics and nosological considerations.

作者信息

Gilman S, Barrett R E

出版信息

J Neurol Sci. 1973 Jun;19(2):189-205. doi: 10.1016/0022-510x(73)90162-7.

DOI:10.1016/0022-510x(73)90162-7
PMID:4712933
Abstract
摘要

相似文献

1
Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Clinical characteristics and nosological considerations.
J Neurol Sci. 1973 Jun;19(2):189-205. doi: 10.1016/0022-510x(73)90162-7.
2
Infantile neuroaxonal dystrophy and its relationship to Hallervorden-Spatz disease.
Neurology. 1968 Jul;18(7):693-9. doi: 10.1212/wnl.18.7.693.
3
Amyotrophic lateral sclerosis-dementia complex, neuroaxonal dystrophy, and Hallervorden-Spatz disease.
Neurology. 1973 Jan;23(1):35-9. doi: 10.1212/wnl.23.1.35.
4
[Myoclonic form of Hallervorden-Spatz disease. Clinical aspect simulating a subacute spongiform encephalitis].[哈勒沃登-施帕茨病的肌阵挛形式。临床表现类似亚急性海绵状脑病]
Rev Neurol (Paris). 1967 Feb;116(2):184-8.
5
Hallervorden-Spatz disease and infantile neuroaxonal dystrophy. Ultrastructural observations, anatomical pathology and nosology.哈勒沃登-施帕茨病与婴儿神经轴索性营养不良。超微结构观察、解剖病理学与疾病分类学。
J Neurol Sci. 1973 Sep;20(1):7-23. doi: 10.1016/0022-510x(73)90114-7.
6
[The Hallervorden-Spatz Disease].
Nervenarzt. 1966 Nov;37(11):482-93.
7
Unusual late-onset type of hallervorden-Spatz disease. Clinico-pathological study of a case presenting as parkinsonism.
Z Neurol. 1972;203(2):105-18. doi: 10.1007/BF00316039.
8
Hallervorden Spatz disease. Its pathogenesis and place among the axonal dystrophies.
Acta Neuropathol. 1966 Mar 4;6(2):164-74. doi: 10.1007/BF00686761.
9
[Hallervorden-Spatz disease with Lewy bodies].
Rev Neurol (Paris). 1985;141(12):806-9.
10
Hallervorden-Spatz syndrome.
Arch Neurol. 1974 Jan;30(1):70-83. doi: 10.1001/archneur.1974.00490310072012.

引用本文的文献

1
Atypical dopa responsive parkinsonism in a patient with megalencephaly, midbrain Lewy body disease, and some pathological features of Hallervorden-Spatz disease.一名患有巨脑症、中脑路易体病及具有哈勒沃登-施帕茨病某些病理特征的患者的非典型多巴反应性帕金森综合征
J Neurol Neurosurg Psychiatry. 1996 Nov;61(5):523-7. doi: 10.1136/jnnp.61.5.523.
2
Infantile neuroaxonal dystrophy. Histological and electron microscopical study of two cases.
Acta Neuropathol. 1974;29(2):115-26. doi: 10.1007/BF00684770.
3
Infantile neuroaxonal dystrophy or Seitelberger's disease. IV. Autonomic nervous system involvement: electron microscopic study in two siblings.
Acta Neuropathol. 1974;28(3):261-7. doi: 10.1007/BF00719031.
4
The genetics of primary torsion dystonia.原发性扭转性肌张力障碍的遗传学
Hum Genet. 1990 Jan;84(2):107-15. doi: 10.1007/BF00208922.
5
Infantile neuroaxonal dystrophy (Seitelberger's disease). A light and ultrastructural study.
Acta Neuropathol. 1975;31(3):191-200. doi: 10.1007/BF00684558.
6
Infantile neuroaxonal dystrophy. An electron microscopic study of a case clinically resembling neuronal ceroid-lipofuscinosis.
Acta Neuropathol. 1975;31(1):35-43. doi: 10.1007/BF00696885.