{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,9,21]],"date-time":"2025-09-21T17:48:17Z","timestamp":1758476897221},"reference-count":12,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[1985,3,1]],"date-time":"1985-03-01T00:00:00Z","timestamp":478483200000},"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":[[1985,3]]},"DOI":"10.1007\/bf00442306","type":"journal-article","created":{"date-parts":[[2004,12,10]],"date-time":"2004-12-10T08:53:19Z","timestamp":1102668799000},"page":"301-303","source":"Crossref","is-referenced-by-count":12,"title":["3-Methylglutaconic and 3-methylglutaric aciduria in a patient with suspected 3-methylglutaconyl-CoA hydratase deficiency"],"prefix":"10.1007","volume":"143","author":[{"given":"W.","family":"Lehnert","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Scharf","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"U.","family":"Wendel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1007\/BF00442517","volume":"138","author":"FA Beemer","year":"1982","unstructured":"Beemer FA, Bartlett K, Duran M, Ghneim HK, Wadman SK, Bruinvis L, Ketting D (1982) Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase deficiency in two sibs. Eur J Pediatr 138:351?354","journal-title":"Eur J Pediatr"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"551","DOI":"10.1016\/S0022-3476(82)80698-7","volume":"101","author":"M Duran","year":"1982","unstructured":"Duran M, Beemer FA, Tibosch AS, Bruinvis L, Ketting D, Wadman SK (1982) Inherited 3-methylglutaconic aciduria in two brothers ? Another defect of leucine metabolism. Eur J Pediatr 101:551?554","journal-title":"Eur J Pediatr"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"231","DOI":"10.1007\/BF00441354","volume":"129","author":"J Greter","year":"1978","unstructured":"Greter J, Hagberg B, Steen G, S\ufffdderhjelm U (1978) 3-Methylglutaconic aciduria: Report on a sibship with infantile progressive encephalopathy. Eur J Pediatr 129:231?238","journal-title":"Eur J Pediatr"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"59","DOI":"10.1016\/0009-8981(83)90184-5","volume":"134","author":"B Hagberg","year":"1983","unstructured":"Hagberg B, Hjalmarson O, Lindstedt S, Ransn\ufffds L, Steen G (1983) 3-Methylglutaconic aciduria in two infants. Clin Chim Acta 134:59?67","journal-title":"Clin Chim Acta"},{"key":"CR5","first-page":"476","volume":"329","author":"H Hilz","year":"1985","unstructured":"Hilz H, Knappe J, Ringelmann E, Lynen F (1985) Methylglutaconase, eine neue Hydratase, die am Stoffwechsel verzweigter Carbons\ufffduren beteiligt ist. Biochem Zeitschr 329:476?489","journal-title":"Biochem Zeitschr"},{"key":"CR6","first-page":"356","volume":"191","author":"W Lehnert","year":"1979","unstructured":"Lehnert W, Niederhoff H (1979) Organisation und Durchf\ufffdhrung eines selektiven Sreenings nach Organoacidurien. Klin P\ufffddiat 191:356?359","journal-title":"Klin P\ufffddiat"},{"key":"CR7","doi-asserted-by":"crossref","first-page":"197","DOI":"10.1007\/BF00444305","volume":"128","author":"W Lehnert","year":"1978","unstructured":"Lehnert W, Schuchmann L, Urb\ufffdnek R, Niederhoff H, B\ufffdhm N (1978) Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia. Eur J Pediatr 128:197?205","journal-title":"Eur J Pediatr"},{"key":"CR8","doi-asserted-by":"crossref","first-page":"56","DOI":"10.1007\/BF00442081","volume":"139","author":"W Lehnert","year":"1982","unstructured":"Lehnert W, Wendel U, Lindenmaier S, B\ufffdhm N (1982) Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. Eur J Pediatr 139:56?59","journal-title":"Eur J Pediatr"},{"key":"CR9","unstructured":"Narisawa K, Gibson KM, Sweetman L, Nyhan WL, Wadman SK (1984) Deficiency of 3-methylglutaconyl-CoA hydratase in cultured skin fibroblasts from two siblings with 3-methylglutaconic aciduria. 22nd Annual Symposium, S.S.I.E.M., Newcastle-upon-Tyne, England"},{"key":"CR10","first-page":"371","volume":"10","author":"BH Robinson","year":"1976","unstructured":"Robinson BH, Sherwood WG, Lampty M, Lowden JA (1976) ?-Methylglutaconic aciduria: A new disorder of leucine metabolism. Pediatr Res 10:371","journal-title":"Pediatr Res"},{"key":"CR11","first-page":"440","volume-title":"The metabolic basis of inherited disease","author":"K Tanaka","year":"1983","unstructured":"Tanaka K, Rosenberg LE (1983) Disorders of branched chain amino acids and organic acid metabolism. In: Stanbury JB, Wyngaarden JB, Fredrickson DS, Goldstein JL, Brown MS (eds) The metabolic basis of inherited disease. McGraw-Hill, New York, pp 440?473"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"349","DOI":"10.1016\/0009-8981(76)90552-0","volume":"71","author":"SJ Wysocki","year":"1976","unstructured":"Wysocki SJ, H\ufffdhnel R (1976) 3-hydroxy-3-methylglutaric aciduria: deficiency of 3-hydroxy-3-methyl-glutaryl coenzyme A lyase. Clin Chim Acta 71:349?351","journal-title":"Clin Chim Acta"}],"container-title":["European Journal of Pediatrics"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00442306.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00442306\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00442306","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,4,4]],"date-time":"2019-04-04T00:38:27Z","timestamp":1554338307000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00442306"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1985,3]]},"references-count":12,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1985,3]]}},"alternative-id":["BF00442306"],"URL":"https:\/\/doi.org\/10.1007\/bf00442306","relation":{},"ISSN":["0340-6199","1432-1076"],"issn-type":[{"value":"0340-6199","type":"print"},{"value":"1432-1076","type":"electronic"}],"subject":[],"published":{"date-parts":[[1985,3]]}}}