Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot–Marie–Tooth disease 1A duplication
- 1 August 2000
- journal article
- clinical trial
- Published by Elsevier BV in Neuromuscular Disorders
- Vol. 10 (6), 419-424
- https://doi.org/10.1016/s0960-8966(99)00114-5
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Motor Nerve Conduction StudiesJournal Of Clinical Neurophysiology, 1995
- Nerve conduction and biopsy correlation in over 100 consecutive patients with suspected polyneuropathyMuscle & Nerve, 1994
- Hereditary motor and sensory neuropathy type I: Clinical and neurographical features of the 17p duplication subtypeMuscle & Nerve, 1994
- Detection of hereditary motor sensory neuropathy type I in childhood.Journal of Neurology, Neurosurgery & Psychiatry, 1992
- Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot‐Marie‐Tooth disease type 1)Annals of Neurology, 1992
- The application of nerve conduction and clinical studies to genetic counseling in hereditary motor and sensory neuropathy type IMuscle & Nerve, 1989
- Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1Muscle & Nerve, 1989
- THE HYPERTROPHIC FORMS OF HEREDITARY MOTOR AND SENSORY NEUROPATHYBrain, 1987
- Prevalence of hereditary motor and sensory neuropathy in CantabriaActa Neurologica Scandinavica, 1987
- Pathogenesis of Pes Cavus in Charcot-Marie-Tooth DiseaseClinical Orthopaedics and Related Research, 1983