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[A further contribution to the knowledge of the Hallervorden-Spatz disease].

作者信息

Gallyas F, Környey S

出版信息

Arch Psychiatr Nervenkr (1970). 1968;212(1):33-45. doi: 10.1007/BF00341968.

DOI:10.1007/BF00341968
PMID:5733780
Abstract
摘要

相似文献

1
[A further contribution to the knowledge of the Hallervorden-Spatz disease].
Arch Psychiatr Nervenkr (1970). 1968;212(1):33-45. doi: 10.1007/BF00341968.
2
Hallervorden-Spatz syndrome.
Arch Neurol. 1974 Jan;30(1):70-83. doi: 10.1001/archneur.1974.00490310072012.
3
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.
4
Hallervorden Spatz disease. Its pathogenesis and place among the axonal dystrophies.
Acta Neuropathol. 1966 Mar 4;6(2):164-74. doi: 10.1007/BF00686761.
5
[The Hallervorden-Spatz Disease].
Nervenarzt. 1966 Nov;37(11):482-93.
6
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.
7
[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.
8
Hallervorden-Spatz disease with bilateral involvement of globus pallidus and substantia nigra: MR demonstration.苍白球和黑质双侧受累的Hallervorden-Spatz病：磁共振成像表现
J Comput Assist Tomogr. 1993 Nov-Dec;17(6):961-3. doi: 10.1097/00004728-199311000-00019.
9
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.
10
[Case of parkinsonism with degeneration of the outer globus pallidus--relationship to progressive atrophy of globus pallidus and Hallervorden-Spatz disease].
Rinsho Shinkeigaku. 1972 Jul;12(7):339-45.

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A novel C19ORF12 mutation in two MPAN sisters treated with deferiprone.两例患多发性神经鞘瘤病姐妹患者应用地拉罗司治疗时发现的新型 C19ORF12 突变。
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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
[CONTRIBUTION TO LATE INFANTILE HALLERVORDEN-SPATZ DISEASE].
Acta Neuropathol. 1963 Sep 2;3:16-28. doi: 10.1007/BF00684016.
3
[METABOLIC DISORDERS IN HALLERVORDEN-SPATZ DISEASE].[哈勒沃登-施帕茨病中的代谢紊乱]
Arch Psychiatr Nervenkr. 1964 Mar 16;205:178-91. doi: 10.1007/BF00352877.
ASN Neuro. 2014 Jan 30;6(1):e00136. doi: 10.1042/AN20130037.
4
AN ELECTRON MICROSCOPIC STUDY OF DYSTROPHIC AXONS IN THE GRACILE AND CUNEATE NUCLEI OF VITAMIN E-DEFICIENT RATS.维生素E缺乏大鼠薄束核和楔束核中营养不良性轴突的电子显微镜研究
J Neuropathol Exp Neurol. 1964 Jan;23:60-77. doi: 10.1097/00005072-196401000-00005.
5
A study of iron metabolism in neuropsychiatric patients. Hallervorden-Spatz disease.
Arch Neurol. 1966 Apr;14(4):438-42. doi: 10.1001/archneur.1966.00470100094012.
6
Infantile neuroaxonal dystrophy. (Seitelberger's disease). Report of an autopsy case.
Acta Neuropathol. 1965 Oct 4;5(1):1-15. doi: 10.1007/BF00689158.
7
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.