References
- Cha, C. H., & Patten, B. M. (1989). Amyotrophic lateral sclerosis: Abnormalities of the tongue on magnetic resonance imaging. Annals of Neurology, 25, 468–472.
- DiLazzaro, V., Restuccia, D., Servirei, S., Valeriani, M., Nardone, R., Manfredi, G., Silvestri, G., Ricci, E., & Tonali, P. (1997). Functional involvement of central nervous system in mitochondrial disorders. Electroencephalography and Clinical Neurophysiology, 105, 171–180.
- Finsterer, J. (2001). Visually evoked potentials in respiratory chain disorders. Acta Neurologica Scandinavia, 104, 31–35.
- Finsterer, J., Eichberger, H., & Jarius, C. (2000). Lactate stress testing in 54 patients with respiratory chain disorder. European Archives of Psychiatric and Clinical Neuroscience, 250, 36–39.
- Finsterer, J., Fuglsang-Frederiksen, A., & Mamoli, B. (1997). Needle EMG of the tongue: Motor unit action potential versus peak ratio analysis in limb and bulbar onset amyotrophic lat- eral sclerosis. Journal of Neurology, Neurosurgery, and Psychiatry, 63, 175–180.
- Janetta, P. J., & Robbins, L. J. (1980). Trigeminal neuropathy—new observations. Neuro- surgery, 7, 347–351.
- Khan, A. R., Bertonini, T. E., & Corner, L. H. (1997). Tongue involvement in a patient with granulomatous myositis. Southern Medical Journal, 90, 937–939.
- Kiliaridis, S., & Katsaros, C. (1998). The effects of myotonic dystrophy and Duchenne muscular dystrophy on the orofacial muscles and dentofacial morphology. Acta Odontol Scandinavia, 56, 369–374.
- Leonard, J. V., & Schapira, A. H. V. (2000). Mitochondrial respiratory chain disorders I: Mitochondrial DNA defects. Lancet, 355, 299–304.
- Salih, M. A., Al Rayess, M., Cutshall, S., Urtizberea, J. A., Al-Turaiki, M. H., Ozo, C. O., Straub, V., Akbar, M., Abid, M., Andeejani, A., & Campbell, K. P. (1998). A novel form of familial congenital muscular dystrophy in two adolescents. Neuropediatrics, 29, 289–293.
- Souies, B. C. (1997). Evaluation and treatment of speech and swallowing disorders asso- ciated with myopathies. Current Opinions in Rheumatology, 9, 486–495.
- Stöllberger, C., Finsterer, J., Keller, H., Mamoli, B., & Slany, J. (1998). Progression of cardiac involvement in patients with myotonic dystrophy, Becker’s muscular dystro- phy and mitochondrial myopathy during a two year follow-up. Cardiology, 90, 173–179.
- Van Goethem, G., Martin, J.-J., & Löfgren, A. (1997). Unusual presentation and clinical variability in Belgian pedigrees with progressive external ophthalmoplegia and mul- tiple deletions of mitochondrial DNA. European Journal of Neurology, 4, 476–484.