References
- Berenberg R. A., Pellock J. M., Dimauro S., et al. Lumping or splitting? Ophthalmoplegia plus or Kearns-Sayre syndrome?. Ann. Neurol. 1977; l: 37–54
- Burns E. C, Preece M. A., Cameron N., et al. Growth hormone deficiency in mitochondrial cytopathy. Actapaediat. scand. 1982; 71: 693–697
- Butler I. J., Gadoth N. Kearns-Sayre syndrome. A review of a multisystem disorder of children and young adults. Arch, intern. Med. 1976; 136: 1290–1293
- Drachman D. A. Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia. Arch. Neurol. 1968; 18: 654–674
- Egger J., Lake D. B., Wilson J. Mitochondrial cytopathy. A multisystem disorder with red fibres on muscle biopsy. Arch. Dis. Child. 1981; 56: 741–752
- Kearns T. P. External ophthalmoplegia, pigmentary degeneration of the retina and cardiomyopathy: a newly recognized syndrome. Trans Amer. ophthal. Soc. 1965; 63: 559–625
- Olson W., Engel W. K., Walsh G. O., et al. Oculocraniosomatic neuromuscular disease with ‘raggedred fibres’. Arch. Neurol. 1972; 26: 193–211
- Pinckers A. J. Leber's congenital amaurosis as conceived by Leber. Ophthalmologic! 1979; 199: 38–51
- Schnitzler E. R., Robertson W. C. Familial Kearns-Sayre syndrome. Neurology 1979; 29: 1172–1174
- Stanescu B., Ferrlere G. Electroretinographic alteration in progressive external ophthalmoplegia, Kearns-Sayre's syndrome. Dev. in Neurol. 1981; 5: 215–221