References
- Déjérine J, Sottas L. Sur la névrite interstitielle hypertrophique et progressive de l'enfance. C R Soc Biol (Paris) 1893; 45: 246–8
- Dyck P J, Lambert E. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. Arch Neurol 1968; 18: 603–25
- Ouvier R, McLeod J, Pollard J. Peripheral Neuropathy in Childhood. Raven Press, New York 1990
- Benstead T, Kuntz N, Miller R, Daube J. The electrophysiologic profile of Déjérine-Sottas disease (HMSN III). Muscle Nerve 1990; 13: 586–92
- Sladky J, Brown M, Berman P. Chronic inflammatory demyelinating polyneuropathy of infancy: A corticosteroid-responsive disorder. Ann Neurol 1986; 20: 76–81
- Bird S, Sladky J. Corticosteroid-responsive dominantly inherited neuropathy in childhood. Neurology 1991; 41: 437–9
- Prensky A, Dodson W. The steroid treatment of hereditary motor and sensory neuropathy. Neuropediatrics 1984; 15: 203–7
- Chan C, Mohsenin V, Loke J, Virgulto J, Sipski L, Ferranti R. Diaphragmatic dysfunction in siblings with hereditary motor sensory neuropathy (Charcot-Marie-Tooth disease). Chest 1987; 91: 567–70
- Gilchrist D, Chan C, Deck J. Phrenic involvement in Charcot-Marie-Tooth disease: A pathologic documentation. Chest 1989; 96: 1197–9
- Hardie R, Harding A, Hirsch N, Gelder C, Macrae A, Thomas P. Diaphragmatic weakness in hereditary motor and sensory neuropathy. J Neurol Neurosurg Psychiatry 1990; 53: 348–50
- Laroche C, Carroll N, Moxham J, Stanley N, Courtney Evans R, Green M. Diaphragm weakness in Charcot-Marie-Tooth disease. Thorax 1988; 43: 478–9
- Eichacker P, Spiro A, Sherman M, Lazar E, Reichel J, Dodick F. Respiratory muscle dysfunction in hereditary motor sensory neuropathy, type, I. Arch Intern Med 1988; 148: 1739–40
- Nathanson B, Ding-Guo Y, Chan C. Respiratory muscle weakness in Charcot-Marie-Tooth disease: A field study. Arch Intern Med 1989; 149: 1389–91