Should Charcot-Marie-Tooth disease be genetically subgrouped on motor conduction velocity.
作者信息
Salisachs P, Findley L J, Codina M, Martinez-Lage J M
出版信息
J Neurol Neurosurg Psychiatry. 1982 Feb;45(2):182-4. doi: 10.1136/jnnp.45.2.182.
Abstract
摘要
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Should Charcot-Marie-Tooth disease be genetically subgrouped on motor conduction velocity.夏科-马里-图思病是否应根据运动传导速度进行基因亚组分类。
J Neurol Neurosurg Psychiatry. 1982 Feb;45(2):182-4. doi: 10.1136/jnnp.45.2.182.
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本文引用的文献
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NERVE CONDUCTION AND OTHER STUDIES IN FAMILIES WITH CHARCOT-MARIE-TOOTH DISEASE.夏科-马里-图思病家族中的神经传导及其他研究
Brain. 1964 Dec;87:589-608. doi: 10.1093/brain/87.4.589.
2
The clinical features of hereditary motor and sensory neuropathy types I and II.遗传性运动和感觉神经病I型和II型的临床特征。
Brain. 1980 Jun;103(2):259-80. doi: 10.1093/brain/103.2.259.
3
[Relations of nerve conduction velocity to histologic findings in peripheral nerves. Based on 49 biopsies of the sural nerve].
Dtsch Z Nervenheilkd. 1965 Dec 14;187(8):770-86.
4
Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.伴有腓骨肌萎缩的下运动神经元和初级感觉神经元疾病。II. 各种神经元变性的神经学、遗传学和电生理发现。
Arch Neurol. 1968 Jun;18(6):619-25. doi: 10.1001/archneur.1968.00470360041003.
5
Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity.腓骨肌萎缩症的运动神经传导速度：遗传异质性的证据
J Neurol Neurosurg Psychiatry. 1974 Jan;37(1):68-75. doi: 10.1136/jnnp.37.1.68.
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Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.伴有腓骨肌萎缩的下运动神经元和原发性感觉神经元疾病。I. 遗传性多发性神经病的神经学、遗传学和电生理发现。
Arch Neurol. 1968 Jun;18(6):603-18. doi: 10.1001/archneur.1968.00470360025002.
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Charcot-Marie-Tooth disease associated with "essential tremor": Report of 7 cases and a review of the literature.与“特发性震颤”相关的夏科-马里-图思病：7例报告及文献复习
J Neurol Sci. 1976 May;28(1):17-40. doi: 10.1016/0022-510x(76)90045-9.
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Charcot-Marie-Tooth disease associated with 'essential tremor' and normal and/or slightly diminished motor conduction velocity. Report of 7 cases.与“特发性震颤”相关且运动传导速度正常和/或轻度减慢的夏科-马里-图思病。7例报告。
Eur Neurol. 1979;18(1):49-58. doi: 10.1159/000115053.
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Heredopathia atactica polyneuritiformis (phytanic acid storage disease). A new case with special reference to dietary treatment.
Arch Intern Med. 1975 Apr;135(4):585-7.
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