{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,21]],"date-time":"2026-09-21T11:32:08Z","timestamp":1789990328513,"version":"4.0.1"},"reference-count":8,"publisher":"Springer Science and Business Media LLC","issue":"4","license":[{"start":{"date-parts":[[1995,8,1]],"date-time":"1995-08-01T00:00:00Z","timestamp":807235200000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatr Nephrol"],"published-print":{"date-parts":[[1995,8]]},"DOI":"10.1007\/bf00866732","type":"journal-article","created":{"date-parts":[[2004,12,27]],"date-time":"2004-12-27T14:32:06Z","timestamp":1104157926000},"page":"476-477","source":"Crossref","is-referenced-by-count":22,"title":["Acute renal failure due to xanthine stones"],"prefix":"10.1007","volume":"9","author":[{"given":"M. G.","family":"Bradbury","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M.","family":"Henderson","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J. T.","family":"Brocklebank","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H. A.","family":"Simmonds","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1007\/BF00850222","volume":"3","author":"HA Simmonds","year":"1989","unstructured":"Simmonds HA, Cameron JS, Barratt TM, Dillon MJ, Meadow SR, Trompeter RS (1989) Purine enzyme defects as a cause of acute renal failure in childhood. Pediatr Nephrol 3:433?437","journal-title":"Pediatr Nephrol"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"328","DOI":"10.1159\/000180910","volume":"19","author":"RA Frayha","year":"1977","unstructured":"Frayha RA, Salti JS, Arnaout AK (1977) Hereditary xanthinuria. Nephron 19:328?332","journal-title":"Nephron"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1007\/BF00441580","volume":"133","author":"W Fuhrmann","year":"1980","unstructured":"Fuhrmann W, Fuhrmann-Rieger A, Sousa F de (1980) Poly-, synand oligodactyly, aplasia or hypoplasia of fibula, hypoplasia of pelvis and bowing of femora in three sibs?a new autosomal recessive syndrome. Eur J Pediatr 133:123?129","journal-title":"Eur J Pediatr"},{"key":"CR4","first-page":"1085","volume-title":"The metabolic basis of inherited disease","author":"EW Holmes","year":"1989","unstructured":"Holmes EW, Wyngaarden JB (1989) Hereditary xanthinuria. In: Scriver CR, Beaudet AL, Sly WS, Valle D, (eds) The metabolic basis of inherited disease, 6th edn. McGraw-Hill, New York p 1085","edition":"6th edn"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1016\/S0022-3476(86)80391-2","volume":"109","author":"TO Carpenter","year":"1986","unstructured":"Carpenter TO, Lebowitz MD, Nelson D (1986) Hereditary xanthinuria presenting in infancy with nephrolithiasis. J Pediatr 109: 307?309","journal-title":"J Pediatr"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1016\/S0022-3476(89)80083-6","volume":"115","author":"RD Fildes","year":"1989","unstructured":"Fildes RD (1989) Hereditary xanthinuria with severe urolithiasis occurring in infancy as renal tubular acidosis and hypercalciuria. J Pediatr 115:277?280","journal-title":"J Pediatr"},{"issue":"Suppl 1","key":"CR7","doi-asserted-by":"crossref","first-page":"78","DOI":"10.1007\/BF01811328","volume":"6","author":"SK Wadman","year":"1983","unstructured":"Wadman SK, Duran M, Beemer FA (1983) Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to combined deficiency of sulphite oxidase and xanthine dehydrogenase. J Interited Metab Dis 6 [Suppl 1]:78?83","journal-title":"J Interited Metab Dis"},{"key":"CR8","doi-asserted-by":"crossref","first-page":"780","DOI":"10.1016\/0002-9343(68)90210-6","volume":"45","author":"JE Seegmiller","year":"1968","unstructured":"Seegmiller JE (1968) Xanthine stone formation. Am J Med 45: 780?783","journal-title":"Am J Med"}],"container-title":["Pediatric Nephrology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00866732.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF00866732\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF00866732","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,4,27]],"date-time":"2019-04-27T00:02:09Z","timestamp":1556323329000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF00866732"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1995,8]]},"references-count":8,"journal-issue":{"issue":"4","published-print":{"date-parts":[[1995,8]]}},"alternative-id":["BF00866732"],"URL":"https:\/\/doi.org\/10.1007\/bf00866732","relation":{},"ISSN":["0931-041X","1432-198X"],"issn-type":[{"value":"0931-041X","type":"print"},{"value":"1432-198X","type":"electronic"}],"subject":[],"published":{"date-parts":[[1995,8]]}}}