[Ischialgia--peroneal muscular atrophy. Points about the disease picture of Tooth's type of progressive muscular atrophy and Déjerine-Sottas syndrome (author's transl)].

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作者信息

Ross A, Schrader A

出版信息

Arch Orthop Unfallchir. 1974 Apr 30;78(2):160-7. doi: 10.1007/BF00416888.

DOI:10.1007/BF00416888

PMID:4275870

Abstract

摘要

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本文引用的文献

NERVE CONDUCTION AND OTHER STUDIES IN FAMILIES WITH CHARCOT-MARIE-TOOTH DISEASE.

Brain. 1964 Dec;87:589-608. doi: 10.1093/brain/87.4.589.

Sensory and motor conduction velocity in the median nerve in the Charcot-Marie-Tooth disease.

Acta Neurol Scand. 1970;46(S43):197-8. doi: 10.1111/j.1600-0404.1970.tb02182.x.

An evaluation of the facial and trigeminal nerves in polyneuropathy: electrodiagnostic study in Charcot-Marie-Tooth disease, Guillain-Barré syndrome, and diabetic neuropathy.

Neurology. 1971 Jul;21(7):745-52. doi: 10.1212/wnl.21.7.745.

[Clinical pathogenetic aspects of diabetic polyneuropathy].

Munch Med Wochenschr. 1972 Nov 17;114(46):2017-24.

Study of the dispersion of motor nerve conduction velocity in charcot-marie-tooth-hoffmann disease and in steinert's syndrome.

Z Neurol. 1972;201(3):211-7. doi: 10.1007/BF00316413.

A comparative clinical and electrophysiological study of Charcot-Marie-Tooth disease and of Friedreich's ataxia.

Electroencephalogr Clin Neurophysiol. 1971 Apr;30(4):369.

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