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E., Clement, D. H., and Provence, S. A. (1974). Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development. Pediatrics, 53, 391-395.","journal-title":"Pediatrics"},{"key":"ref_2","first-page":"378","article-title":"Genetic complementation of propionyl CoA carboxylase deficiency in cultured human fibroblasts","volume":"29","author":"Gravel, R.A.; Lam, K.F.; Scully, K.J.; Hsia, Y.E.","year":"1977","unstructured":"Gravel, R. A., Lam, K. F., Scully, K. J., and Hsia, Y. E. (1977). Genetic complementation of propionyl CoA carboxylase deficiency in cultured human fibroblasts. American Journal ofHuman Genetics, 29, 378-388.","journal-title":"American Journal ofHuman Genetics"},{"key":"ref_3","first-page":"411","article-title":"Disorders of propionate, methylmalonate, and cobalamin metabolism","volume-title":"The Metabolic Basis of Inherited Disease, fourth","author":"Rosenberg, L.E.","year":"1978","unstructured":"Rosenberg, L. E. (1978). Disorders of propionate, methylmalonate, and cobalamin metabolism. In The Metabolic Basis of Inherited Disease, fourth edition, pp. 411-429. Edited by J. B. Stanbury, J. B. Wyngaarden, and D. S. Fredrickson. McGraw-Hill: New York."},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"281","DOI":"10.1542\/peds.53.2.281","article-title":"Letter: Reduction of plasma propionate by peritoneal dialysis","volume":"53","author":"Russell, G.; Thorn, H.; Tarlow, M.J.; Gompertz, D.","year":"1974","unstructured":"Russell, G., Thorn, H., Tarlow, M. J., and Gompertz, D. (1974). Letter: Reduction of plasma propionate by peritoneal dialysis. Pediatrics, 53, 281-283.","journal-title":"Pediatrics"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"1044","DOI":"10.1016\/S0022-3476(73)80440-8","article-title":"Peritoneal clearance of ammonia and creatinine in a neonate","volume":"82","author":"Siegel, N.J.; Brown, R.S.","year":"1973","unstructured":"Siegel, N. J., and Brown, R. S. (1973). Peritoneal clearance of ammonia and creatinine in a neonate. Journal ofPediatrics, 82, 1044-1046.","journal-title":"Journal ofPediatrics"},{"key":"ref_6","first-page":"707","article-title":"Hyperglycemia and propionyl CoA carboxylase deficiency and episodic severe illness without ketosis","volume":"86","author":"Wadlington, W.B.; Kilroy, A.; Ando, T.; Sweetman, L.; Nyhan, W.L.","year":"1975","unstructured":"Wadlington, W. B., Kilroy, A., Ando, T., Sweetman, L., and Nyhan, W. L. (1975). Hyperglycemia and propionyl CoA carboxylase deficiency and episodic severe illness without ketosis. Journal ofPediatries, 86, 707-712.","journal-title":"Journal ofPediatries"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"931","DOI":"10.1172\/JCI109221","article-title":"Heterzygote expression in propionyl coenzyme A carboxylase deficiency: differences between major complementation groups","volume":"62","author":"Wolf, B.; Rosenberg, L.E.","year":"1978","unstructured":"Wolf, B., and Rosenberg, L. E. (1978). Heterzygote expression in propionyl coenzyme A carboxylase deficiency: differences between major complementation groups. Journal of Clinical Investigation, 62, 931-936.","journal-title":"Journal of Clinical Investigation"},{"key":"ref_8","article-title":"With the recent development of techniques for testing thyroid activity, some interesting neonatal cases of thyroid dysfunction have been found. One of the most important developments in this field has been the introduction of mass screening for neonatal hypothyroidism, and several mass screening programmes have been reported. We have developed a new 'paired TSH assay method'","author":"et al. (1977) and Delange et al.","year":"1978","unstructured":"With the recent development of techniques for testing thyroid activity, some interesting neonatal cases of thyroid dysfunction have been found. One of the most important developments in this field has been the introduction of mass screening for neonatal hypothyroidism, and several mass screening programmes have been reported. We have developed a new 'paired TSH assay method' (Miyai et al., 1978). We were able to screen 91 400 babies between November 1975 and September 1978, and found 9 cases of primary hypothyroidism. We also found a boy who had high TSH but normal levels of thyroid hormones in the serum for 7 months, but whose TSH level decreased spontaneously to within normal limits after 9 months. This syndrome, which apparently differs from the transient neonatal hypothyroidism reported by La Franchi et al. (1977) and Delange et al. (1978), is described.","journal-title":"(Miyai et al; We were able to screen 91 400 babies between November 1975 and September 1978, and found 9 cases of primary hypothyroidism. We also found a boy who had high TSH but normal levels of thyroid hormones in the serum for 7 months, but whose TSH level decreased spontaneously to within normal limits after 9 months. This syndrome, which apparently differs from the transient neonatal hypothyroidism reported by La Franchi"}],"container-title":["Archives of Disease in Childhood"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/adc.54.12.962","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,23]],"date-time":"2023-05-23T03:44:32Z","timestamp":1684813472000},"score":1,"resource":{"primary":{"URL":"https:\/\/adc.bmj.com\/lookup\/doi\/10.1136\/adc.54.12.962"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1979,12,1]]},"references-count":8,"journal-issue":{"issue":"12","published-print":{"date-parts":[[1979,12,1]]}},"URL":"https:\/\/doi.org\/10.1136\/adc.54.12.962","relation":{},"ISSN":["0003-9888","1468-2044"],"issn-type":[{"value":"0003-9888","type":"print"},{"value":"1468-2044","type":"electronic"}],"subject":[],"published":{"date-parts":[[1979,12,1]]}}}