Hereditary spastic paraplegia with amyotrophy and pes cavus.
作者信息
GARLAND H G, ASTLEY C E
出版信息
J Neurol Neurosurg Psychiatry. 1950 May;13(2):130-3. doi: 10.1136/jnnp.13.2.130.
Abstract
摘要
相似文献
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Hereditary spastic paraplegia with amyotrophy and pes cavus.伴有肌萎缩和高弓足的遗传性痉挛性截瘫
J Neurol Neurosurg Psychiatry. 1950 May;13(2):130-3. doi: 10.1136/jnnp.13.2.130.
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Familial periodic paralysis, myotonia, progressive amyotrophy, and pes cavus in members of a single family.一个家族成员中出现的家族性周期性麻痹、肌强直、进行性肌萎缩和高弓足。
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引用本文的文献
1
Addison's disease in association with spastic paraplegia.
Br Med J. 1960 Feb 6;1(5170):402. doi: 10.1136/bmj.1.5170.402.
2
HEREDITARY SPASTIC PARAPLEGIA.遗传性痉挛性截瘫
J Neurol Neurosurg Psychiatry. 1963 Dec;26(6):516-9. doi: 10.1136/jnnp.26.6.516.
3
Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred.
J Neurol Neurosurg Psychiatry. 1994 Nov;57(11):1343-6. doi: 10.1136/jnnp.57.11.1343.
4
Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families.遗传性“单纯”痉挛性截瘫：22个家系的临床与遗传学研究
J Neurol Neurosurg Psychiatry. 1981 Oct;44(10):871-83. doi: 10.1136/jnnp.44.10.871.
5
Manifesting heterozygosity in sex-linked spastic paraplegia?在X连锁痉挛性截瘫中表现为杂合性？
J Neurol Neurosurg Psychiatry. 1984 Mar;47(3):311-3. doi: 10.1136/jnnp.47.3.311.
6
Peroneal muscular atrophy with pyramidal features.伴有锥体束征的腓骨肌萎缩症
J Neurol Neurosurg Psychiatry. 1984 Feb;47(2):168-72. doi: 10.1136/jnnp.47.2.168.
7
Strümpell's familial spastic paraplegia: genetics and neuropathology.施特吕姆佩尔家族性痉挛性截瘫：遗传学与神经病理学
J Neurol Neurosurg Psychiatry. 1974 Jan;37(1):8-20. doi: 10.1136/jnnp.37.1.8.
8
Peroneal muscular atrophy with hereditary spastic paraparesis (HMSN V) is pathologically heterogeneous. Report of nerve biopsy in four cases and review of the literature.伴有遗传性痉挛性截瘫的腓骨肌萎缩症（遗传性运动感觉神经病V型）在病理上具有异质性。4例神经活检报告及文献综述。
Acta Neuropathol. 1992;83(2):196-201. doi: 10.1007/BF00308479.
9
X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg.一个大家系中的X连锁隐性型单纯性痉挛性截瘫：与Xg无明显连锁关系。
J Med Genet. 1976 Jun;13(3):217-22. doi: 10.1136/jmg.13.3.217.
10
Electrophysiological studies in familial spastic paraplegia.家族性痉挛性截瘫的电生理研究
J Neurol Neurosurg Psychiatry. 1977 Jun;40(6):611-5. doi: 10.1136/jnnp.40.6.611.
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