Intermediate Charcot–Marie–Tooth disease: an electrophysiological reappraisal and systematic review

Author:

Berciano José,García Antonio,Gallardo Elena,Peeters Kristien,Pelayo-Negro Ana L.,Álvarez-Paradelo Silvia,Gazulla José,Martínez-Tames Miriam,Infante Jon,Jordanova Albena

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Reference156 articles.

1. Combarros O, Calleja J, Polo JM, Berciano J (1987) Prevalence of hereditary motor and sensory neuropathy in Cantabria. Acta Neurol Scand 75:9–12

2. Dyck PJ (2005) Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory, and autonomic neurons. In: Dyck PJ, Thomas PK, Lambert EH, Bunge R (eds) Peripheral neuropathy, 2nd edn. WB Saunders, Philadelphia, pp 1600–1655

3. Harding AE, Thomas PK (1980) The clinical features of hereditary motor and sensory neuropathy types I and II. Brain 103:259–280

4. Davis CJ, Bradley WG, Madrid R (1978) The peroneal muscular atrophy syndrome: clinical, genetic, electrophysiological and nerve biopsy studies. I. Clinical, genetic and electrophysiological findings and classification. J Genet Hum 26:311–349

5. Madrid R, Bradley WG, Davis CJ (1977) The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies. Observations on pathological changes in sural nerve biopsies. J Neurol Sci 32:91–122

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