References
- Babel J. Ophthalmological aspects of myotonic dystrophy. Neurogenetics and Neuro-Ophthalmology, A Huber, D Klein. Elsevier/North Holland Biomedical Press, Amsterdam 1981; 19–30
- Miller NR. Myopathies and disorders of neuromuscular transmission. Walsh and Hoyi's Clinical Neuro-Ophthalmology. 4th edn. Williams and Wilkins, Baltimore 1985; vol 2: 785–891
- Ketelsen U-P, Schmidt D. Augensymptome und elektronmikroskopische Befunde des M. orbicularis oculi bei dys-trophischer Myotonie (Curschmann-Steinert). Albrecht von Graefes Arch Klin Exp Ophthalmol 1972; 185: 245–268
- Kuwabara T, Lessel S. Electron microscopic study of extraocular muscles in myotonic dystrophy. Am J Ophthalmol 1976; 82: 303–309
- Johnson MA. Skeletal muscle. Histochemistry in Pathology, MI Filipe, BD Lake. Churchill Livingstone, Edinburgh 1983; 89–113
- Bresno N, Massimo Z, Bonila E, Miller RH, Leech RH, Shanske S, Nakagawa M, DiMauro S. Fatal infantile cytochrome c oxidase deficiency: Decrease of immunologically detectable enzyme in muscle. Neurology 1985; 35: 802–812
- Carpenter S, Karpati G. Myotonic dystrophy-adult. Pathology of Skeletal Muscle, FL Mastaglia, JN Walton. Churchill Livingstone, New York/Edinburgh/London/Melbourne 1984; 612–628
- Ono S, Kirposjo H, Inoue K, Mannen T. 'Ragged-red' fibres in myotonic dystrophy. J Neurol Sci 1986; 74: 247–255
- Sengers RCA, Stadhouders AM, Trijbels JMF. Mitochondrial myopathies. Clinical, morphological and biochemical aspects. Eur. J Pediat 1984; 141: 192–207
- McKusick VA. Myotonic dystrophy. Mendelian Inheritance in Man. The Johns Hopkins University Press, Baltimore 1983; 509–511
- DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC. Mitochondrial myopathies. Ann Neurol 1985; 17: 521–538
- Ogier H, Roels F, Cornelis A, Poll The Bt, Scotto JM., Odievre M., Sandbray JM. Absence of hepatic peroxisomes in a case of infantile Refsum's disease. Scand Clin Lab Invest 1985; 45: 767–768
- Thomas GH, Haslam RHA, Bathshaw ML, Capute AJ, Meidengard L, Ransom JL. Hyperpipecolic acidemia associated with hepatomcgaly, mental retardation, optic nerve dysplasia and progressive neurologic disease. Clin Genet 1975; 3: 376–381
- Burton BK, Reed SP, Remy WT. Hyperpipecolic acidemia :clinical and biochemical observations in two male siblings. J Pediat 1981; 99: 729–734
- Hittner HM, Kretzer F, Metha RS. Zcllweger's syndrome, lenticular opacities indicating carrier lens abnormalities charac-teristic of homozygotes. Arch Ophthalmol 1982; 99: 1977–1982
- Kretzer F, Hittner HM, Metha R. Ocular manifestations of Conradi and Zellweger's syndromes. Metab Pediat Ophthalmol 1981; 5: 1–11