Defects of metabolism of fatty acids in the sudden infant death syndrome.
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Sinclair-Smith CC, Dinsdale F, Emery JL. Evidence of duration and type of illness in children found unexpectedly dead. Arch Dis Child 1976;51:424-9.
Reye RDK, Morgan G, Baral J. Encephalopathy and fatty degeneration of the viscera: a disease entity in childhood. Lancet 1963;ii:749-52.
Partin JC, Bove K, Partin JS, Schubert WK. Liver and muscle ultrastructure in Reye's syndrome. In: Crocker JFS, ed. Reye's syndrome II. New York: Grune and Stratton, 1979:217-37.
Delong GR, Glick TH. Encephalopathy of Reye's syndrome: a review of pathogenetic hypotheses. Pediatrics 1982;69:53-63.
Brandt NJ. Symptoms and signs in organic acidurias. Journal of Inherited Metabolic Disease 1984;7(suppl 1):23-7.
Mowat AP. Reye's syndrome: 20 years on. Br MedJ7 1983;286:1999-2001.
Bove KE, McAdams AJ, Partin JC, Partin JS, Hug G, Schubert WK. The hepatic lesion in Reye's syndrome. Gastroenterology 1975;69:685-97.
Mitchell RA, Ram ML, Arcinue EL, Chang CH. Comparison of cytosolic and mitochondrial hepatic enzyme alterations in Reye's syndrome. Pediatr Res 1980;14:1216-21.
Corey L, Rubin RJ, Bregman D, Gregg MB. Diagnostic criteria for influenza B-associated Reye's syndrome. Clinical vs pathologic criteria. Pediatrics 1977; 60:702-8.
Hall S, Bellman MH. Reye's syndrome in the British Isles BPA/CDSC surveillance scheme. Communicable Disease Report 1983;39:3-6.
Howat AJ, Bennett MJ, Variend S, Shaw L. Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome. Br MedJa 1984;288:976.
Filipe MI, Lake BD, eds. Histochemistry in pathology. Edinburgh, London, Melbourne, New York: Churchill Livingstone, 1983:318-32.
Shaw L, Engel PC. The purification and properties of ox liver short-chain acyl-CoA dehydrogenase. Biochem 1984;218:511-20.
Stanley CA, Hale DE, Coates PM, et al. Medium-chain acyl-CoA dehydrogenase deficiex.cy in children with non-ketotic hypoglycemia and low carnitine levels. Pediatr Res 1983;17:877-84.
Duran M, De Klerk JBC, Wadman SK, Bruinvis L, Ketting D. The differential diagnosis of dicarboxylic aciduria. Journal of Inherited Metabolic Disease 1984;7(suppl 1):48-51.
Peterson DR. Epidemiology of the sudden infant death syndrome: problems, progress and prospects. A review. In: Tildon JT, Roeder LM, Steinschneider A, eds. Sudden infant death syndrome. New York, London: Academic Press, 1983:89-97.
Sherratt HSA, Veitch RK. Animal models for dicarboxylic aciduria. Journal of Inherited Metabolic Disease 1984;7(suppl 1):52-6.
Bergman AB, Beckwith JB, Ray CG. Proceedings of the second international conference on cause of sudden death in infants. Seattle: University of Washington Press, 1970. (Accepted 14 March 1985)
Changes in incidence and prognosis of ischaemic heart disease in Finland: a record linkage study of data on death certificates and hospital records for 1972 and 1981
The components of the decline in mortality from ischaemic heart disease in Finland were studied by analysing the changes in incidence and prognosis between 1972 and 1981. Using personal identification numbers, hospital discharge records and death certificates were linked for all men and women aged 40-64. During this period mortality decreased 15 9% in men and 23 5% in women, incidence 14.2% in men and 19-3% in women, being greatest among 40-49 year olds living in urban areas, and case fatality Department of Public Health Science, University of Helsinki, 00290 Helsinki 29, Finland
The epidemic of ischaemic heart disease in industrialised countries has been waning in some countries while waxing in others over the past 10-15 years.'-7 Ischaemic heart disease mortality has been declining in Finland since 1969-70 by a yearly 2%.8 9 This decline may be due either to factors improving the prognosis of incident cases or to a decline in incidence of the disease. Because data on changes in incidence of ischaemic heart disease world wide are few we examined data on admission to hospital for and mortality from ischaemic heart disease in Finland for 1972 and 1981 to assess relative changes in mortality, survival, and incidence.