1. Barbeau, A.: The syndrome of hereditary late onset ptosis and dysphagia in French Canada. In: Progressive Muskeldystrophie, Myotonie, Myasthenie, pp. 102?109, Kuhn, E. (ed.). Berlin, Heidelberg, New York: Springer 1966
2. Brooke, M. H.: A clinician's view of neuromuscular diseases, pp. 123?124. Baltimore: Williams and Wilkins 1977
3. Fardeau, M.: Caractéristiques cytochimiques et ultrastructurales des différents types de fibres musculaires squelettiques extra-fusales (chez l'homme et quelques mammifères) Ann. Anat. Pathol. (Paris)18, 7?34 (1973)
4. Fardeau, M., Tomé, F. M. S.: The skeletal muscle. In: Electron microscopy in human medicine, Vol. 4, Johannessen, J. V. (ed.). New York: McGraw-Hill (in press)
5. Julien, J., Vital, Cl., Vallat, J. M., Le Blanc, M.: Oculopharyngeal muscular dystrophy. A case with abnormal mitochondria and ?fingerprint? inclusions. J. Neurol. Sci.21, 165?169 (1974)