{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T03:44:25Z","timestamp":1764992665212,"version":"3.46.0"},"reference-count":7,"publisher":"BMJ","issue":"9","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Clin Pathol"],"published-print":{"date-parts":[[2000,9]]},"abstract":"<jats:p>Primary hyperoxaluria is a rare genetic disorder characterised by calcium oxalate nephrolithiasis and nephrocalcinosis leading to renal failure, often with extrarenal oxalate deposition (systemic oxalosis). Although ischaemic complications of crystal deposition in vessel walls are well recognised clinically, these usually take the form of peripheral limb or cutaneous ischaemia. This paper documents the first reported case of fatal intestinal infarction in a 49 year old woman with systemic oxalosis and advocates its consideration in the differential diagnosis of an acute abdomen in such patients.<\/jats:p>","DOI":"10.1136\/jcp.53.9.720","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T06:37:59Z","timestamp":1027751879000},"page":"720-721","source":"Crossref","is-referenced-by-count":8,"title":["Small intestinal infarction: a fatal complication of systemic oxalosis: \n            Figure 1"],"prefix":"10.1136","volume":"53","author":[{"given":"J S","family":"Johnson","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A K","family":"Short","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A","family":"Hutchison","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"N R","family":"Parrott","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I S D","family":"Roberts","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","published-online":{"date-parts":[[2000,9,1]]},"reference":[{"key":"2025120518353721000_53.9.720.1","doi-asserted-by":"publisher","DOI":"10.1046\/j.1523-1755.1999.00477.x"},{"key":"2025120518353721000_53.9.720.2","unstructured":"Williams HE, Smith LH. Primary hyperoxaluria. In: Stanbury JB, Wyngaarden, JB, Fredrickson DS, et al, eds. The metabolic basis of inherited disease, 5th ed. New York: McGraw-Hill, 1983."},{"key":"2025120518353721000_53.9.720.3","doi-asserted-by":"publisher","DOI":"10.1002\/art.1780310919"},{"key":"2025120518353721000_53.9.720.4","doi-asserted-by":"publisher","DOI":"10.1016\/0002-9343(73)90126-5"},{"key":"2025120518353721000_53.9.720.5","doi-asserted-by":"publisher","DOI":"10.1001\/archderm.1995.01690190075014"},{"key":"2025120518353721000_53.9.720.6","doi-asserted-by":"publisher","DOI":"10.1097\/00000478-199701000-00007"},{"key":"2025120518353721000_53.9.720.7","doi-asserted-by":"crossref","first-page":"576","DOI":"10.1055\/s-0038-1665259","volume":"50","year":"1983","journal-title":"Thromb Haemost"}],"container-title":["Journal of Clinical Pathology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jcp.53.9.720","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T02:35:41Z","timestamp":1764988541000},"score":1,"resource":{"primary":{"URL":"https:\/\/jcp.bmj.com\/lookup\/doi\/10.1136\/jcp.53.9.720"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2000,9]]},"references-count":7,"journal-issue":{"issue":"9","published-online":{"date-parts":[[2000,9,1]]},"published-print":{"date-parts":[[2000,9]]}},"alternative-id":["10.1136\/jcp.53.9.720"],"URL":"https:\/\/doi.org\/10.1136\/jcp.53.9.720","relation":{},"ISSN":["0021-9746","1472-4146"],"issn-type":[{"type":"print","value":"0021-9746"},{"type":"electronic","value":"1472-4146"}],"subject":[],"published":{"date-parts":[[2000,9]]}}}