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[Studies on familial spastic paraplegia. III. The Tib family...; very early forms of familial spastic paraplegia with idiocy and oligophrenia in collateral branches of the family].

作者信息

APPEL L, VAN BOGAERT L

出版信息

Acta Neurol Psychiatr Belg. 1951 Nov;51(11):716-30.

PMID:14894181
Abstract
摘要

相似文献

1
[Studies on familial spastic paraplegia. III. The Tib family...; very early forms of familial spastic paraplegia with idiocy and oligophrenia in collateral branches of the family].[家族性痉挛性截瘫的研究。III. 蒂布家族……；家族旁系中伴有白痴和智力发育不全的家族性痉挛性截瘫的极早期形式]
Acta Neurol Psychiatr Belg. 1951 Nov;51(11):716-30.
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Familial spastic paraplegia with amyotrophy, oligophrenia, and central retinal degeneration.伴有肌萎缩、智力发育迟缓及中心性视网膜变性的家族性痉挛性截瘫
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[Familial spastic paraplegia].[家族性痉挛性截瘫]
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Sem Med. 1956 Sep 27;109(15):642-9; passim.
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Familial spastic paraplegia, mental retardation, and precocious puberty.家族性痉挛性截瘫、智力发育迟缓与性早熟。
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Hereditary spastic paraplegia and hereditary ataxia: a family demonstrating a variety of phenotypic manifestations.
AMA Arch Neurol Psychiatry. 1951 Sep;66(3):346-54. doi: 10.1001/archneurpsyc.1951.02320090095008.
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Hereditary spastic paraplegia.遗传性痉挛性截瘫
South Med J. 1957 Aug;50(8):1065-7. doi: 10.1097/00007611-195708000-00021.
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Homocarnosinosis. 2. A familial metabolic disorder associated with spastic paraplegia, progressive mental deficiency, and retinal pigmentation.
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Genetical investigations in a north-Swedish population; population structure, spastic oligophrenia, deaf mutism.对瑞典北部人群的遗传学研究；人群结构、痉挛性智力发育不全、聋哑症
Ann Hum Genet. 1956 Feb;20(3):239-50. doi: 10.1111/j.1469-1809.1956.tb01369.x.
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[Familial spastic paraplegia with mental deficiency in two sisters; Schilder's disease?].[两姐妹患伴有智力缺陷的家族性痉挛性截瘫；席尔德病？]
Rev Neurol (Paris). 1951;85(4):280-2.

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