Dominantly inherited motor and sensory neuropathy type I
- 1 October 1983
- journal article
- research article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 61 (2) , 181-191
- https://doi.org/10.1016/0022-510x(83)90004-7
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhoodMuscle & Nerve, 1981
- Genetic aspects of hereditary motor and sensory neuropathy (types I and II)Journal of Medical Genetics, 1980
- THE CLINICAL FEATURES OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPES I AND IIBrain, 1980
- Charcot‐Marie‐Tooth disease: Data for genetic counseling relating age to riskClinical Genetics, 1978
- PERONEAL MUSCULAR ATROPHY (PMA) AND RELATED DISORDERSBrain, 1977
- Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy)*Annals of Human Genetics, 1974
- Wide spectrum of motor conduction velocity in charcot-marie-tooth diseaseJournal of the Neurological Sciences, 1974
- Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneityJournal of Neurology, Neurosurgery & Psychiatry, 1974
- Evoked action potentials and conduction velocity in human sensory nervesBrain Research, 1966
- NERVE CONDUCTION AND OTHER STUDIES IN FAMILIES WITH CHARCOT-MARIE-TOOTH DISEASEBrain, 1964