References
- Azizi E., Zaidman J. L., Eshchar J., Szeinberg A. Abetalipoproteinaemia treated with parenteral and oral vitamins A and E, and with medium chain triglycerides. Acta pad. scand 1978; 67: 797–801
- Bergsma D. Birth Defects, Atlas and Compendium. The National Foundation-March of Dimes. White Plains, New York 1973
- Chhabria S, Tomasi L. G., Lloyd-Still J. D. Neurological manifestations of cystic fibrosis: lack of relationship to vitamin E deficiency. Abstract. Ann. Neurol 1978; 4: 194
- Drachman D. A. Ophthalmoplegia plus. The neurodegenerative disorders associated with progressive external ophthalmoplegia. Arch. Neurol (Chicago) 1968; 18: 654–674
- Elias E., Muller D. P. R., Scott J. Association of spinocerebellar disorders with cystic fibrosis or chronic childhood cholestasis and very low serum vitamin E. Lancet ii 1981; 1319–1321
- Farrell P. M, Bieri J. G, Fratantoni J. F., Wood R. E., DiSantagnese P. A. The occurrence and effects of human vitamin E deficiency. J. clin. Invest 1977; 60: 233–241
- Geller A., Gilles F., Schwachman H. Degeneration of fasciculus gracilis in cystic fibrosis. Neurologr 1977; 27: 185–187
- Herbert P. N, Gotto A. M., Fredrickson D. S. Familial lipoprotein deficiency (abetalipoproteinaemia, hypobetalipoproteinaemia, and Tangier disease). The Metabolic Basis of Inherited Disease 4th edn., J. B. Stanbury, J. B. Wijngaarden, D. S. Fredrickson. McGraw-Hill Book Company, New York 1978; 544–588
- Hoogenraad T. U, Tan K. E. W. P., Eelderink H. J. W, Veldman H., Jennekens F. G. I. The inferior oblique as muscle of choice for biopsies of extraocular muscles. Brit. J. Ophthal 1979; 63: 680–683
- Illingworth D. R., Connor W. E., Miller R. G. Abetalipoproteinemia. Report of two cases and review of therapy. Arch. Neurol. (Chicago) 1980; 37: 659–662
- Martinek R. G. Method for the determination of vitamin E (total tocopherols) in serum. Clin. Chem 1964; 10: 1078–1086
- Muller D. P. R., Lloyd J. K., Bird A. C. Long-term management of abetalipoproteinaemia. Arch. Dis. Childh 1977; 52: 209–214
- Nadler L, Rao J. A., Taussig L. M. The Metabolic Basis of Inherited Disease. Cystic fibrosis, J. B. Stanbury, J. B. Wijngaarden, D. S. Fredrickson. McGraw-Hill Book Company, New York 1978; 1683–1710
- Pentschew A., Schwarz K. Systemic axonal dystrophy in vitamin E deficient adult rats, with implication in human neuropathology. Acta neuropath. (Berlin) 1962; 7: 313–334
- Rosenblum J. L, Keatink J. P., Prensky A. L., Nelson J. S. A progressive neurologic syndrome in children with chronic liver disease. New Engl. J. Med 1981; 304: 503–508
- Santagnese P. A. Di, Davis P. B. Research in cystic fibrosis. New Engl. J. Med 1976; 295: 481–485; 534–541; 597–602
- Santagnese P. A. Di, Davis P. B. Cystic fibrosis in adults, 75 cases and a review of 232 cases in the literature. Amer. J. Med 1979; 66: 121–132
- Sung J. H. Neuroaxonal dystrophy in mucoviscidosis. J Neuropath, exp. Neurol 1964; 23: 567–583
- Sung J. H., Park S. H., Mastri A. R., Warwick W. J. Axonal dystrophy in the gracile nucleus in congenital biliary atresia and cystic fibrosis (mucoviscidosis): beneficial effect of vitamin E therapy. J. Neuropath, exp. Neurol 1980; 39: 584–597
- Tomasi L. G. Reversibility of human myopathy caused by vitamin E deficiency. Neurology 1979; 29: 1182–1186
- Troost J. Fucosidosis, a Clinical, Enzymological and Ultra-structural Study. Elinkwijk bv, Utrecht 1977