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[Friedreich's ataxia with peripheral nerve involvement resembling peroneal muscular atrophy].

作者信息

Hopf H C, Port F K

出版信息

Dtsch Z Nervenheilkd. 1968;194(1):1-16.

PMID:4300543
Abstract
摘要

相似文献

1
[Friedreich's ataxia with peripheral nerve involvement resembling peroneal muscular atrophy].[伴有类似腓骨肌萎缩症的周围神经受累的弗里德赖希共济失调]
Dtsch Z Nervenheilkd. 1968;194(1):1-16.
2
Association of Friedreich's ataxia and peroneal muscular atrophy (familial ataxia with atrophy). Report of two cases.
J Assoc Physicians India. 1969 Feb;17(2):123-6.
3
A case of Charcot-Marie-Tooth disease mimicking Friedreich's ataxia: is there any association between friedreich's ataxia and Charcot-Marie-Tooth disease?一例酷似弗里德赖希共济失调的夏科-马里-图斯病：弗里德赖希共济失调与夏科-马里-图斯病之间存在关联吗？
Can J Neurol Sci. 1982 May;9(2):99-103. doi: 10.1017/s0317167100043778.
4
Necrotizing encephalomyelopathy. Report of a case with relapsing polyneuropathy and hyperalaninemia and with manifestations resembling Friedreich's ataxia.
Neurology. 1969 Jun;19(6):536-50. doi: 10.1212/wnl.19.6.536.
5
[Syndrome of myatrophic ataxia].[肌萎缩性共济失调综合征]
Psychiatr Neurol Med Psychol (Leipz). 1972 Apr;24(4):177-88.
6
[Studies on nerve conduction in neural muscular atrophy and Friedreich's hereditary ataxia].[关于神经肌肉萎缩和弗里德赖希遗传性共济失调中神经传导的研究]
Dtsch Z Nervenheilkd. 1969;195(3):166-86.
7
The primary spino-cerebellar atrophies and their associated defects, with a study of the foot deformity.原发性脊髓小脑萎缩及其相关缺陷，附足部畸形研究
Brain. 1961 Jun;84:289-300. doi: 10.1093/brain/84.2.289.
8
[So-called Friedreich's foot (author's transl)].
Klin Padiatr. 1977 Sep;189(5):302-8.
9
Clinical and electrodiagnostic features of Charcot-Marie-Tooth syndrome.夏科-马里-图思综合征的临床及电诊断特征
Acta Neurol Scand Suppl. 1978;68:1-142.
10
[Electroencephalographic changes in certain cases of neural amyotrophy and in so-called Friedreich's disease].[某些神经性肌萎缩病例及所谓弗里德赖希氏病的脑电图变化]
Cesk Neurol. 1960 Jun;23:239-45.

引用本文的文献

1
[Investigations of peripheral and central somatosensory pathways in peroneal muscular atrophy and Friedreich's heredoataxia (author's transl)].腓骨肌萎缩症和弗里德赖希遗传性共济失调中外周和中枢躯体感觉通路的研究（作者译）
Arch Psychiatr Nervenkr (1970). 1980;228(3):223-42. doi: 10.1007/BF00342348.
2
Peroneal muscular atrophy with ataxia and partial myoclonic epilepsy.伴有共济失调和部分肌阵挛性癫痫的腓骨肌萎缩症
J Neurol. 1981;226(1):1-13. doi: 10.1007/BF00313313.
3
[Studies on nerve conduction in neural muscular atrophy and Friedreich's hereditary ataxia].

本文引用的文献

1
Peroneal Atrophy, with Signs of Friedreich's Disease.腓骨肌萎缩症，伴弗里德赖希氏病体征。
Proc R Soc Med. 1912;5(Neurol Sect):75-6. doi: 10.1177/003591571200500813.
2
Three Brothers, illustrating an Unusual Form of Family Paralysis (Familial Lateral Sclerosis with Amyotrophy).《三兄弟》，阐述一种罕见的家族性麻痹形式（伴有肌萎缩的家族性侧索硬化症）
Proc R Soc Med. 1912;5(Neurol Sect):144-8. doi: 10.1177/003591571200500828.
3
Heredofamilial cerebellar ataxia with spastic paralysis and spinal muscular atrophy; report of two cases of an unusual syndrome.
[关于神经肌肉萎缩和弗里德赖希遗传性共济失调中神经传导的研究]
Dtsch Z Nervenheilkd. 1969;195(3):166-86.
4
[Hereditary cerebellar aataxia with spinal muscular atrophies].[伴有脊髓性肌萎缩的遗传性小脑共济失调]
Z Neurol. 1971;199(4):344-52.
5
Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases.脊髓小脑变性中的肥厚性神经病。14例腓浅神经的形态学研究。
Acta Neuropathol. 1987;75(1):51-61. doi: 10.1007/BF00686793.
6
[Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)].[腓骨肌萎缩症（夏科-马里-图思病）时骨骼肌的线粒体变化。组织学和电子显微镜研究（作者译）]
J Neurol. 1975;209(1):9-29. doi: 10.1007/BF00312522.
伴有痉挛性瘫痪和脊髓性肌萎缩的遗传性家族性小脑共济失调；一种罕见综合征的两例报告。
J Nerv Ment Dis. 1949 May;109(5):409-17. doi: 10.1097/00005053-194910950-00004.
4
On a possible relationship between hereditary ataxia and peroneal muscular atrophy; with a critical review of the problems of intermediate forms in the degenerative disorders of the central nervous system.论遗传性共济失调与腓骨肌萎缩症之间的可能关系；对中枢神经系统退行性疾病中间型问题的批判性综述。
Brain. 1948 Dec;71(Pt. 4):416-33. doi: 10.1093/brain/71.4.416.
5
[An unusual spino-cerebellar heredo-degenerative sequence].
G Psichiatr Neuropatol. 1952;80(1):37-70.
6
[Forms of heredo-ataxia of children and adolescents with severe involvement of the spinobulbomesencephalic motor nuclei].[伴有延髓脑桥中脑运动核严重受累的儿童及青少年遗传性共济失调的类型]
Rev Neurol (Paris). 1951 Feb;84(2):121-30.
7
[Case of Friedreich disease with Charcot-Marie amyotrophy clinical study].[伴有夏科-马里肌萎缩的弗里德赖希共济失调病临床研究病例]
Rev Neurol (Paris). 1950 Oct;83(4):281-4.
8
Familial ataxia, deaf-mutism, and muscular wasting.家族性共济失调、聋哑症和肌肉萎缩。
J Neurol Neurosurg Psychiatry. 1950 Nov;13(4):307-11. doi: 10.1136/jnnp.13.4.307.
9
[Distal amyotrophy of the Charcot-Marie type with nystagmus; clinical study and muscle biopsies].[伴有眼球震颤的夏科-马里型远端肌萎缩症；临床研究与肌肉活检]
Rev Neurol (Paris). 1954;91(5):358-61.
10
Connections between neural muscle atrophy and hereditary ataxia (Friedreich).神经肌肉萎缩与遗传性共济失调（弗里德赖希氏病）之间的关联。
Med Klin. 1955 Apr 15;50(15):638-40.