{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,11,20]],"date-time":"2024-11-20T05:39:18Z","timestamp":1732081158440,"version":"3.28.0"},"reference-count":20,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,11,19]]},"DOI":"10.7759\/cureus.74028","type":"journal-article","created":{"date-parts":[[2024,11,19]],"date-time":"2024-11-19T22:09:27Z","timestamp":1732054167000},"source":"Crossref","is-referenced-by-count":0,"title":["A Case of Hyperammonemia Not Attributable to Liver Disease and Treated With IV Ammonia Scavengers"],"prefix":"10.7759","author":[{"given":"Joel","family":"Thomas","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Astly","family":"George","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sharmin","family":"Mrittika","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Bilal","family":"Ahmad","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Gisela","family":"Wilcox","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1002\/jimd.12292","article-title":"A retrospective study of adult patients with noncirrhotic hyperammonemia","volume":"43","author":"Stergachis AB","year":"2020","unstructured":"Stergachis AB, Mogensen KM, Khoury CC, et al.. A retrospective study of adult patients with noncirrhotic hyperammonemia. J Inherit Metab Dis. 2020, 43:1165-72. 10.1002\/jimd.12292","journal-title":"J Inherit Metab Dis"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1093\/omcr\/omu027","article-title":"Acute hyperammonaemic encephalopathy","volume":"2014","author":"Ng PS","year":"2014","unstructured":"Ng PS, Lim CC, Tan NC. Acute hyperammonaemic encephalopathy. Oxf Med Case Reports. 2014, 2014:69-70. 10.1093\/omcr\/omu027","journal-title":"Oxf Med Case Reports"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.3390\/nu15102284","article-title":"Citrin deficiency: clinical and nutritional features","volume":"15","author":"Komatsu M","year":"2023","unstructured":"Komatsu M, Tanaka N, Kimura T, Yazaki M. Citrin deficiency: clinical and nutritional features. Nutrients. 2023, 15:2284. 10.3390\/nu15102284","journal-title":"Nutrients"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.3390\/jcm10132773","article-title":"The cerebral effect of ammonia in brain aging: blood-brain barrier breakdown, mitochondrial dysfunction, and neuroinflammation","volume":"10","author":"Jo D","year":"2021","unstructured":"Jo D, Kim BC, Cho KA, Song J. The cerebral effect of ammonia in brain aging: blood-brain barrier breakdown, mitochondrial dysfunction, and neuroinflammation. J Clin Med. 2021, 10:2773. 10.3390\/jcm10132773","journal-title":"J Clin Med"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1016\/0887-8994(86)90016-0","article-title":"Neurologic syndromes in hyperammonemic disorders","volume":"2","author":"Breningstall GN","year":"1986","unstructured":"Breningstall GN. Neurologic syndromes in hyperammonemic disorders. Pediatr Neurol. 1986, 2:253-62. 10.1016\/0887-8994(86)90016-0","journal-title":"Pediatr Neurol"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1007\/s11154-018-9455-2","article-title":"Impact of pregnancy on inborn errors of metabolism","volume":"19","author":"Wilcox G","year":"2018","unstructured":"Wilcox G. Impact of pregnancy on inborn errors of metabolism. Rev Endocr Metab Disord. 2018, 19:13-33. 10.1007\/s11154-018-9455-2","journal-title":"Rev Endocr Metab Disord"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1258\/acb.2011.011206","article-title":"Severe hyperammonaemia in adults not explained by liver disease","volume":"49","author":"Walker V","year":"2012","unstructured":"Walker V. Severe hyperammonaemia in adults not explained by liver disease. Ann Clin Biochem. 2012, 49:214-28. 10.1258\/acb.2011.011206","journal-title":"Ann Clin Biochem"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1055\/s-2007-1007315","article-title":"Inherited and acquired syndromes of hyperammonemia and encephalopathy in children","volume":"14","author":"Treem WR","year":"1994","unstructured":"Treem WR. Inherited and acquired syndromes of hyperammonemia and encephalopathy in children. Semin Liver Dis. 1994, 14:236-58. 10.1055\/s-2007-1007315","journal-title":"Semin Liver Dis"},{"key":"ref9","doi-asserted-by":"crossref","DOI":"10.1016\/S0065-3101(24)00072-0","article-title":"Urea cycle disorders: diagnosis, pathophysiology, and therapy","volume":"43","author":"Brusilow SW","year":"1996","unstructured":"Brusilow SW, Maestri NE. Urea cycle disorders: diagnosis, pathophysiology, and therapy. Adv Pediatr. 1996, 43:127-70.","journal-title":"Adv Pediatr"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.1016\/s1089-3261(05)70143-4","article-title":"Urea cycle disorders","volume":"4","author":"Burton BK","year":"2000","unstructured":"Burton BK. Urea cycle disorders. Clin Liver Dis. 2000, 4:815-30. 10.1016\/s1089-3261(05)70143-4","journal-title":"Clin Liver Dis"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1111\/j.1478-3231.2011.02550.x","article-title":"Noncirrhotic hyperammonaemic encephalopathy","volume":"31","author":"Laish I","year":"2011","unstructured":"Laish I, Ben Ari Z. Noncirrhotic hyperammonaemic encephalopathy. Liver Int. 2011, 31:1259-70. 10.1111\/j.1478-3231.2011.02550.x","journal-title":"Liver Int"},{"key":"ref12","doi-asserted-by":"crossref","DOI":"10.1097\/00005792-199811000-00004","article-title":"The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency","volume":"77","author":"Maestri NE","year":"1998","unstructured":"Maestri NE, Lord C, Glynn M, Bale A, Brusilow SW. The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency. Medicine (Baltimore). 1998, 77:389-97.","journal-title":"Medicine (Baltimore)"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1186\/1750-1172-7-32","article-title":"Suggested guidelines for the diagnosis and management of urea cycle disorders","volume":"7","author":"H\u00e4berle J","year":"2012","unstructured":"H\u00e4berle J, Boddaert N, Burlina A, et al.. Suggested guidelines for the diagnosis and management of urea cycle disorders. Orphanet J Rare Dis. 2012, 7:32. 10.1186\/1750-1172-7-32","journal-title":"Orphanet J Rare Dis"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.1016\/j.ymgme.2009.08.007","article-title":"Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency","volume":"99","author":"Balasubramaniam S","year":"2010","unstructured":"Balasubramaniam S, Rudduck C, Bennetts B, Peters G, Wilcken B, Ellaway C. Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency. Mol Genet Metab. 2010, 99:34-41. 10.1016\/j.ymgme.2009.08.007","journal-title":"Mol Genet Metab"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.1016\/j.jhep.2009.11.014","article-title":"Adult-onset ornithine transcarbamylase (OTC) deficiency unmasked by the Atkins' diet","volume":"52","author":"Ben-Ari Z","year":"2010","unstructured":"Ben-Ari Z, Dalal A, Morry A, et al.. Adult-onset ornithine transcarbamylase (OTC) deficiency unmasked by the Atkins' diet. J Hepatol. 2010, 52:292-5. 10.1016\/j.jhep.2009.11.014","journal-title":"J Hepatol"},{"key":"ref16","article-title":"Ornithine transcarbamylase deficiency","author":"Lichter-Konecki U","year":"1993","unstructured":"Lichter-Konecki U, Caldovic L, Morizono H, Simpson K, Ah Mew N, MacLeod E. Ornithine transcarbamylase deficiency. GeneReviews. 1993,","journal-title":"GeneReviews"},{"key":"ref17","doi-asserted-by":"publisher","DOI":"10.3390\/nu12113313","article-title":"Dietary management, clinical status and outcome of patients with citrin deficiency in the UK","volume":"12","author":"Pinto A","year":"2020","unstructured":"Pinto A, Ashmore C, Batzios S, et al.. Dietary management, clinical status and outcome of patients with citrin deficiency in the UK. Nutrients. 2020, 12:3313. 10.3390\/nu12113313","journal-title":"Nutrients"},{"key":"ref18","doi-asserted-by":"publisher","DOI":"10.1515\/med-2021-0235","article-title":"Adult-onset citrullinaemia type II with liver cirrhosis: a rare cause of hyperammonaemia","volume":"16","author":"Chen P","year":"2021","unstructured":"Chen P, Gao X, Chen B, Zhang Y. Adult-onset citrullinaemia type II with liver cirrhosis: a rare cause of hyperammonaemia. Open Med (Wars). 2021, 16:455-8. 10.1515\/med-2021-0235","journal-title":"Open Med (Wars)"},{"key":"ref19","doi-asserted-by":"publisher","DOI":"10.1136\/jcp-2022-208644","article-title":"Drug-induced hyperammonaemia","volume":"76","author":"Shakerdi L","year":"2023","unstructured":"Shakerdi L, Ryan A. Drug-induced hyperammonaemia. J Clin Pathol. 2023, 76:501-9. 10.1136\/jcp-2022-208644","journal-title":"J Clin Pathol"},{"key":"ref20","doi-asserted-by":"publisher","DOI":"10.1016\/j.ymgme.2013.09.003","article-title":"Dietary management of urea cycle disorders: European practice","volume":"110","author":"Adam S","year":"2013","unstructured":"Adam S, Almeida MF, Assoun M, et al.. Dietary management of urea cycle disorders: European practice. Mol Genet Metab. 2013, 110:439-45. 10.1016\/j.ymgme.2013.09.003","journal-title":"Mol Genet Metab"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/307022-a-case-of-hyperammonemia-not-attributable-to-liver-disease-and-treated-with-iv-ammonia-scavengers","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,11,19]],"date-time":"2024-11-19T22:09:29Z","timestamp":1732054169000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/307022-a-case-of-hyperammonemia-not-attributable-to-liver-disease-and-treated-with-iv-ammonia-scavengers"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,11,19]]},"references-count":20,"URL":"https:\/\/doi.org\/10.7759\/cureus.74028","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2024,11,19]]}}}