CLINICAL AND ELECTRODIAGNOSTIC FEATURES OF CHARCOT-MARIE-TOOTH SYNDROME
- 1 July 1978
- journal article
- Published by Hindawi Limited in Acta Neurologica Scandinavica
- Vol. 58 (s68) , 4-142
- https://doi.org/10.1111/j.1600-0404.1978.tb07640.x
Abstract
No abstract availableThis publication has 87 references indexed in Scilit:
- New method for the estimation of the number of motor units in a muscle: 2. Duchenne, limb-girdle and facioscapulohumeral, and myotonic muscular dystrophiesJournal of Neurology, Neurosurgery & Psychiatry, 1974
- Ocular myasthenia gravis mimicking progressive external ophthalmoplegiaNeurology, 1974
- THE FAMILIAL ASSOCIATION OF NEUROFIBROMATOSIS, PERONEAL MUSCULAR ATROPHY, CONGENITAL DEAFNESS, PARTIAL ALBINISM, AND AXENFELD'S DEFECTBrain, 1974
- Myotonic dystrophy with neural involvementJournal of the Neurological Sciences, 1972
- Spino-Pontine DegenerationEuropean Neurology, 1969
- Hereditary spastic ataxia with central retinal degeneration and vestibular impairmentNeurology, 1962
- Neural Muscle Atrophy with Degeneration of the Substantia NigraStereotactic and Functional Neurosurgery, 1955
- HEREDITARY SPASTIC PARAPLEGIAJournal of Neurology, Neurosurgery & Psychiatry, 1950
- Der erbliche MuskelschwundZeitschrift für die gesamte Neurologie und Psychiatrie, 1938
- ON HEREDITARY ATAXY, WITH A SERIES OF TWENTY-ONE CASESBrain, 1892