Degenerative ataxic disorders: still perplexing.
作者信息
Harding A
机构信息
University Department of Clinical Neurology, Institute of Clinical Neurology, London.
出版信息
Br Med J (Clin Res Ed). 1987 Nov 14;295(6608):1223-4. doi: 10.1136/bmj.295.6608.1223-a.
Abstract
摘要
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本文引用的文献
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Adrenoleukomyeloneuropathy presenting as spinocerebellar degeneration.表现为脊髓小脑变性的肾上腺脑白质营养不良症。
Neurology. 1982 Sep;32(9):1031-2. doi: 10.1212/wnl.32.9.1031.
2
Friedreich ataxia: III. Mitochondrial malic enzyme deficiency.
Neurology. 1982 Mar;32(3):221-7. doi: 10.1212/wnl.32.3.221.
3
Biochemical and clinical studies of Friedreich's ataxia.弗里德赖希共济失调的生化与临床研究。
J Neurol Neurosurg Psychiatry. 1981 Jul;44(7):574-82. doi: 10.1136/jnnp.44.7.574.
4
Neurological disorders associated with deficiency of glutamate dehydrogenase.与谷氨酸脱氢酶缺乏相关的神经障碍
Ann Neurol. 1984 Feb;15(2):144-53. doi: 10.1002/ana.410150206.
5
Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy.橄榄体脑桥小脑萎缩患者的谷氨酸脱氢酶缺乏症
Neurology. 1983 Oct;33(10):1322-6. doi: 10.1212/wnl.33.10.1332.
6
The Quebec Cooperative Study of Friedreich's Ataxia: 1974-1984--10 years of research.魁北克弗里德赖希共济失调合作研究：1974 - 1984年——十年研究历程
Can J Neurol Sci. 1984 Nov;11(4 Suppl):646-60. doi: 10.1017/s0317167100035228.
7
Long-term treatment of cerebrotendinous xanthomatosis with chenodeoxycholic acid.鹅去氧胆酸对脑腱黄瘤病的长期治疗
N Engl J Med. 1984 Dec 27;311(26):1649-52. doi: 10.1056/NEJM198412273112601.
8
Classification of the hereditary ataxias and paraplegias.遗传性共济失调和截瘫的分类。
Lancet. 1983 May 21;1(8334):1151-5. doi: 10.1016/s0140-6736(83)92879-9.
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Vitamin E and neurological function.维生素E与神经功能。
Lancet. 1983 Jan 29;1(8318):225-8. doi: 10.1016/s0140-6736(83)92598-9.
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Spinocerebellar degeneration associated with a selective defect of vitamin E absorption.与维生素E吸收选择性缺陷相关的脊髓小脑变性
N Engl J Med. 1985 Jul 4;313(1):32-5. doi: 10.1056/NEJM198507043130107.
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