{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,11,3]],"date-time":"2023-11-03T22:28:31Z","timestamp":1699050511440},"reference-count":31,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1978,1,1]],"date-time":"1978-01-01T00:00:00Z","timestamp":252460800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Eur J Pediatr"],"published-print":{"date-parts":[[1978]]},"DOI":"10.1007\/bf00442159","type":"journal-article","created":{"date-parts":[[2004,11,12]],"date-time":"2004-11-12T03:30:08Z","timestamp":1100230208000},"page":"157-165","source":"Crossref","is-referenced-by-count":9,"title":["Maple syrup urine disease: Treatment of the acutely ill newborn"],"prefix":"10.1007","volume":"129","author":[{"given":"G.","family":"Hammersen","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L.","family":"Wille","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Schmidt","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P.","family":"Lutz","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"Bickel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","first-page":"809","volume":"11","author":"J. Chemke","year":"1975","unstructured":"Chemke, J., Levin, S.: Maple syrup urine disease. Two cases in Israel. Israel J. Med. Sci. 11, 809?816 (1975)","journal-title":"Israel J. Med. Sci."},{"key":"CR2","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1542\/peds.25.1.72","volume":"25","author":"J. Dancis","year":"1960","unstructured":"Dancis, J., Levitz, M., Westall, R. G.: Maple syrup urine disease: branched chain keto aciduria. Pediatrics 25, 72?79 (1960)","journal-title":"Pediatrics"},{"key":"CR3","first-page":"426","volume-title":"The metabolic basis of inherited disease","author":"J. Dancis","year":"1972","unstructured":"Dancis, J., Levitz, M.: Abnormalities of branched chain amino acid metabolism. In: The metabolic basis of inherited disease, J. B. Stanbury, J. B. Wyngarden, D. S. Fredrickson, eds., 3rd ed., pp. 426?439. New York: MeGraw Hill 1972","edition":"3rd ed."},{"key":"CR4","doi-asserted-by":"crossref","first-page":"312","DOI":"10.1016\/S0022-3476(72)80301-9","volume":"81","author":"J. Dancis","year":"1972","unstructured":"Dancis, J., Hutzler, J., Snyderman, S. E., Cox, R. P.: Enzyme activity in classical and variant forms of maple syrup urine disease. J. Pediat. 81, 312?320 (1972)","journal-title":"J. Pediat."},{"key":"CR5","first-page":"123","volume-title":"Antenatal diagnosis","author":"J. Dancis","year":"1972","unstructured":"Dancis, J.: Maple syrup urine disease. In: Antenatal diagnosis. A. Dorfman, ed., pp. 123?125. Chicago: The University of Chicago Press 1972"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"130","DOI":"10.1016\/0006-2944(69)90005-2","volume":"3","author":"G. E. Gaull","year":"1969","unstructured":"Gaull, G. E.: Pathogenesis of maple syrup urine disease: Observations during dietary management and treatment of coma by peritoneal dialysis. Biochem. Med. 3, 130?149 (1969)","journal-title":"Biochem. Med."},{"key":"CR7","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1111\/j.1651-2227.1970.tb15519.x","volume":"59","author":"H. W. Goedde","year":"1970","unstructured":"Goedde, H. W., Langenbeck, U., Brackertz, D., Keller, W., Rokkones, T., Halvorsen, S., Kiil, R., Merton, B.: Clinical and biochemical-genetic aspects of intermittent branched chain ketoaciduria. Acta Paediat. Scand. 59, 83?87 (1970)","journal-title":"Acta Paediat. Scand."},{"key":"CR8","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1016\/S0022-3476(69)80278-7","volume":"75","author":"S. I. Goodman","year":"1969","unstructured":"Goodman, S. I., Pollak, S., Miles, B., O'Brien, D.: The treatment of maple syrup urine disease. J. Pediat. 75, 485?488 (1969)","journal-title":"J. Pediat."},{"key":"CR9","doi-asserted-by":"crossref","unstructured":"Harris, J. R.: Infection in maple syrup urine disease. Lancet 1971 II, 813?814","DOI":"10.1016\/S0140-6736(71)92760-7"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"356","DOI":"10.1111\/j.1651-2227.1964.tb07789.x","volume":"53","author":"R. Kiil","year":"1964","unstructured":"Kiil, R., Rokkones, T.: Late manifesting variant of branched chain ketoaciduria (maple syrup urine disease). Acta Paediat. Scand. 53, 356?364 (1964)","journal-title":"Acta Paediat. Scand."},{"key":"CR11","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1007\/BF00464456","volume":"116","author":"P. Koepp","year":"1974","unstructured":"Koepp, P., Rybak, C., R\ufffddiger, H. W., Wendel, U.: Maple syrup urine disease variant: report of an infant. Z. Kinderheilk. 116, 177?184 (1974) (Europ. J. Pediat.)","journal-title":"Z. Kinderheilk."},{"key":"CR12","first-page":"1","volume-title":"Advances in human genetics","author":"H. L. Levy","year":"1973","unstructured":"Levy, H. L.: Genetic screening. In: Advances in human genetics, H. Harris, K. Hirschhorn, eds., Vol. IV, pp. 1?104. New York: Plenum Press 1973"},{"key":"CR13","doi-asserted-by":"crossref","unstructured":"Mackenzie, D. Y., Woolf, L. I.: Maple syrup urine disease: an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency. Brit. Med. J. 1959 I, 90?91","DOI":"10.1136\/bmj.1.5114.90"},{"key":"CR14","doi-asserted-by":"crossref","first-page":"462","DOI":"10.1542\/peds.14.5.462","volume":"14","author":"J. H. Menkes","year":"1954","unstructured":"Menkes, J. H., Hurst, P. L., Craig, J. M.: A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance. Pediatrics 14, 462?466 (1954)","journal-title":"Pediatrics"},{"key":"CR15","doi-asserted-by":"crossref","first-page":"348","DOI":"10.1542\/peds.23.2.348","volume":"23","author":"J. H. Menkes","year":"1959","unstructured":"Menkes, J. H.: Maple syrup urine disease: isolation and identification of organic acids in the urine. Pediatrics 23, 348?353 (1959)","journal-title":"Pediatrics"},{"key":"CR16","doi-asserted-by":"crossref","first-page":"918","DOI":"10.1542\/peds.28.6.918","volume":"28","author":"M. D. Morris","year":"1961","unstructured":"Morris, M. D., Lewis, B. D., Doolan, P. D., Harper, H. A.: Clinical and biochemical observations on an apparently nonfatal variant of branched chain ketoaciduria (maple syrup urine disease). Pediatrics 28, 918?923 (1961)","journal-title":"Pediatrics"},{"key":"CR17","doi-asserted-by":"crossref","first-page":"1552","DOI":"10.1055\/s-0028-1110178","volume":"96","author":"H. M\ufffdller","year":"1971","unstructured":"M\ufffdller, H., Bickel, H., Feist, D., Lutz, P.: Ahornsirupkrankheit mit intermittierendem, relativ gutartigem Verlauf. Dtsch. Med. Wschr. 96, 1552?1557 (1971)","journal-title":"Dtsch. Med. Wschr."},{"key":"CR18","first-page":"133","volume":"26","author":"F. Rey","year":"1969","unstructured":"Rey, F., Rey, J., Cloup, M., F\ufffdron, J.-F., Dor\ufffd, F., Labrune, B., Fr\ufffdzal, J.: Traitment d'urgence d'une forme aigue de leucinose par dialyse peritoneale. Arch. Franc. P\ufffdd. 26, 133?137 (1969)","journal-title":"Arch. Franc. P\ufffdd."},{"key":"CR19","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1016\/S0021-9258(18)65457-2","volume":"210","author":"W. C. Rose","year":"1954","unstructured":"Rose, W. C., Coon, M. J., Lambert, G. F.: The amino acid requirements of man. VI. The role of the caloric intake. J. Biol. Chem. 210, 331?342 (1954)","journal-title":"J. Biol. Chem."},{"key":"CR20","doi-asserted-by":"crossref","unstructured":"Sallan, S. E., Cottom, D.: Peritoneal dialysis in maple syrup urine disease. Lancet 1969 II, 1423?1424","DOI":"10.1016\/S0140-6736(69)90961-1"},{"key":"CR21","doi-asserted-by":"crossref","first-page":"895","DOI":"10.1055\/s-0028-1105160","volume":"93","author":"C. Sander","year":"1968","unstructured":"Sander, C., Clotten, R., Noetzel, H., Wehinger, H.: Zur Klinik und pathologischen Anatomie der Ahornsirupkrankheit (branched chain ketoaciduria). Dtsch. Med. Wschr. 93, 895?903 (1968)","journal-title":"Dtsch. Med. Wschr."},{"key":"CR22","first-page":"1279","volume":"122","author":"J.-M. Saudubray","year":"1971","unstructured":"Saudubray, J.-M., Fournet, J.-P., Cloup, M.: Int\ufffdr\ufffdt de la dialyse p\ufffdriton\ufffdale dans le traitment d'urgence des maladies m\ufffdtaboliques d'origine constitutionelle r\ufffdv\ufffdl\ufffdes dans la p\ufffdriode n\ufffdonatale. Ann. M\ufffdd. interne 122, 1279?1283 (1971)","journal-title":"Ann. M\ufffdd. interne"},{"key":"CR23","first-page":"449","volume":"27","author":"L. Schuchmann","year":"1972","unstructured":"Schuchmann, L., Witt, I., Schulz, P., Schuhmacher, H., R\ufffddiger, H.: Multiple exchange transfusions as treatment during the acute period in maple syrup urine disease. Helv. Paediat. Acta 27, 449?456 (1972)","journal-title":"Helv. Paediat. Acta"},{"key":"CR24","doi-asserted-by":"crossref","unstructured":"Scriver, C. R., Clow, C. L., Mackenzie, S., Delvin, E.: Thiamine responsive maple syrup urine disease. Lancet 1971 I, 310?312","DOI":"10.1016\/S0140-6736(71)91041-5"},{"key":"CR25","doi-asserted-by":"crossref","first-page":"454","DOI":"10.1542\/peds.34.4.454","volume":"34","author":"C. R. Snyderman","year":"1964","unstructured":"Snyderman, C. R., Norton, P. M., Roitman, E., Holt, L. E.: Maple syrup urine disease, with particular reference to dietotherapy. Pediatrics 34, 454?472 (1964)","journal-title":"Pediatrics"},{"key":"CR26","first-page":"68","volume":"113","author":"S. E. Snyderman","year":"1967","unstructured":"Snyderman, S. E.: The therapy of maple syrup urine disease. Amer. J. Dis. Child. 113, 68?73 (1967)","journal-title":"Amer. J. Dis. Child."},{"key":"CR27","first-page":"71","volume-title":"The treatment of inherited metabolic disease","author":"S. E. Snyderman","year":"1975","unstructured":"Snyderman, S. E.: Maple syrup urine disease. In: The treatment of inherited metabolic disease, D. N. Raine, ed., pp. 71?90. Lancaster, Lancs: Medical and Technical Publishing Co. 1975"},{"key":"CR28","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1136\/adc.48.3.225","volume":"48","author":"H. B. Valman","year":"1973","unstructured":"Valman, H. B., Patrick, A. D., Seakins, J. W. T., Platt, J. W., Gompertz, D.: Family with intermittent maple syrup urine disease. Arch. Dis Child. 48, 225?228 (1973)","journal-title":"Arch. Dis Child."},{"key":"CR29","doi-asserted-by":"crossref","first-page":"127","DOI":"10.1007\/BF00295241","volume":"19","author":"U. Wendel","year":"1973","unstructured":"Wendel, U., R\ufffddiger, H. W., Passarge, E., Mikkelsen, M.: Maple syrup urine disease: Rapid prenatal diagnosis by enzyme assay. Humangenetik 19, 127?128 (1973)","journal-title":"Humangenetik"},{"key":"CR30","first-page":"571","volume":"94","author":"R. G. Westall","year":"1957","unstructured":"Westall, R. G., Dancis, J., Miller, S.: Maple syrup urine disease. Amer. J. Dis. Child. 94, 571?572 (1957)","journal-title":"Amer. J. Dis. Child."},{"key":"CR31","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1136\/adc.38.201.485","volume":"38","author":"R. G. Westall","year":"1963","unstructured":"Westall, R. G.: Dietary treatment of a child with maple syrup urine disease (branched chain ketoaciduria). Arch. Dis. Child. 38, 485?491 (1963)","journal-title":"Arch. Dis. Child."}],"container-title":["European Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00442159.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00442159\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00442159","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,4,30]],"date-time":"2023-04-30T05:04:30Z","timestamp":1682831070000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00442159"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1978]]},"references-count":31,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1978]]}},"alternative-id":["BF00442159"],"URL":"https:\/\/doi.org\/10.1007\/bf00442159","relation":{},"ISSN":["0340-6199","1432-1076"],"issn-type":[{"value":"0340-6199","type":"print"},{"value":"1432-1076","type":"electronic"}],"subject":[],"published":{"date-parts":[[1978]]}}}