{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,4,28]],"date-time":"2023-04-28T16:13:18Z","timestamp":1682698398732},"reference-count":14,"publisher":"Oxford University Press (OUP)","issue":"773","license":[{"start":{"date-parts":[[1990,3,1]],"date-time":"1990-03-01T00:00:00Z","timestamp":636249600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[1990,3,1]]},"abstract":"<jats:title>Summary<\/jats:title>\n               <jats:p>A 52 year old man presented with myoglobinuria-induced acute renal failure requiring dialysis. Despite renal biopsy, the cause of the myoglobinuria was not established until he re-presented a year later with a milder episode. At this stage investigations, including a muscle biopsy, demonstrated a defect in fatty acid oxidation amenable to dietary and lifestyle advice. This report emphasizes the importance of reaching a definitive diagnosis in myoglobinuria.<\/jats:p>","DOI":"10.1136\/pgmj.66.773.235","type":"journal-article","created":{"date-parts":[[2008,12,29]],"date-time":"2008-12-29T21:01:03Z","timestamp":1230584463000},"page":"235-237","source":"Crossref","is-referenced-by-count":1,"title":["Myoglobinuria: the importance of reaching a firm diagnosis\u2014a patient with defective fatty acid oxidation"],"prefix":"10.1093","volume":"66","author":[{"given":"C J","family":"Ellis","sequence":"first","affiliation":[{"name":"Department of Medicine, Royal South Hants Hospital , Lyon Street, Southampton, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A G","family":"Dewhurst","sequence":"additional","affiliation":[{"name":"Department of Medicine, Royal South Hants Hospital , Lyon Street, Southampton, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M","family":"Cooper","sequence":"additional","affiliation":[{"name":"Department of Medicine, Royal South Hants Hospital , Lyon Street, Southampton, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D P","family":"Brenton","sequence":"additional","affiliation":[{"name":"Department of Medicine, University College and Middlesex School of Medicine , University Street, London UK"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J R","family":"Dathan","sequence":"additional","affiliation":[{"name":"Department of Medicine, Royal South Hants Hospital , Lyon Street, Southampton, UK"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"286","published-online":{"date-parts":[[1990,3,1]]},"reference":[{"issue":"66","key":"ref_1","first-page":"173","article-title":"Fatty acid oxidation in mitochondria from needle biopsy samples of human skeletal muscle","volume":"1984","author":"Gohil, K.; Jones, D.A.; Edwards, R.H.T.","unstructured":"Gohil, K., Jones, D.A. & Edwards, R.H.T. Fatty acid oxidation in mitochondria from needle biopsy samples of human skeletal muscle. Clin Sci 1984, 66: 173-178.","journal-title":"Clin Sci"},{"issue":"37","key":"ref_2","first-page":"1184","article-title":"Exercised-induced recurrent myoglobinuria: defective activity of inner carnitine palmityl transferase in muscle mitochondria of two patients","volume":"1987","author":"Trevisan, C.P.; Grazia, I.; Angelini, C.","unstructured":"Trevisan, C.P., Grazia, I. & Angelini, C. Exercised-induced recurrent myoglobinuria: defective activity of inner carnitine palmityl transferase in muscle mitochondria of two patients. Neurology 1987, 37: 1184-1188.","journal-title":"Neurology"},{"issue":"61","key":"ref_3","first-page":"1015","article-title":"Serum creatine phosphokinase (CKP) activity in disorders of heart and skeletal muscle","volume":"1964","author":"Hess, J.W.; MacDonald, R.P.; Frederick, R.J.","unstructured":"Hess, J.W., MacDonald, R.P., Frederick, R.J. et al. Serum creatine phosphokinase (CKP) activity in disorders of heart and skeletal muscle. Ann Intern Med 1964, 61: 1015-1028.","journal-title":"Ann Intern Med"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1097\/00005792-198205000-00002","article-title":"The spectrum of rhabdomyolysis","volume":"61","author":"Gabow, A.P.; Kaehny, W.D.; Kelleher, S.P.","year":"1982","unstructured":"Gabow, A.P., Kaehny, W.D. & Kelleher, S.P. The spectrum of rhabdomyolysis. Medicine 1982, 61: 141-152.","journal-title":"Medicine"},{"key":"ref_5","first-page":"340","article-title":"Skeletal muscle storage diseases: myopathies resulting from errors in carbohydrate and fatty acid metabolism","volume":"10","author":"Pleasure, D.; Bonilla, E.","year":"1982","unstructured":"Pleasure, D. & Bonilla, E. Skeletal muscle storage diseases: myopathies resulting from errors in carbohydrate and fatty acid metabolism. In: Mastalgia, Fl. & Walton, J. (eds) Skeletal Muscle Pathology, vol. 10. Churchill Livingstone, Edinburgh, London 1982, pp. 340-359.","journal-title":"Skeletal Muscle Pathology"},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"1186","DOI":"10.1056\/NEJM197212072872307","article-title":"Caloric homeostasis and disorders of fuel transport","volume":"287","author":"Havel, R.J.","year":"1972","unstructured":"Havel, R.J. Caloric homeostasis and disorders of fuel transport. N Engl J Med 1972, 287: 1186-1192.","journal-title":"N Engl J Med"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"610","DOI":"10.7326\/0003-4819-88-5-610","article-title":"Recurrent myoglobinuria due to muscle carnitine palmityl transferase deficiency","volume":"88","author":"Reza, M.J.; Kar, N.C.; Pearson, C.M.","year":"1978","unstructured":"Reza, M.J., Kar, N.C., Pearson, C.M. et al. Recurrent myoglobinuria due to muscle carnitine palmityl transferase deficiency. Ann Intern Med 1978, 88: 610-615.","journal-title":"Ann Intern Med"},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"263","DOI":"10.1212\/WNL.30.3.263","article-title":"Carnitine palmityl transferase deficiency. Myoglobinuria and respiratory failure","volume":"30","author":"Bertorini, T.; Yeh, Y.; Trevisan, C.","year":"1980","unstructured":"Bertorini, T., Yeh, Y., Trevisan, C. et al. Carnitine palmityl transferase deficiency. Myoglobinuria and respiratory failure. Neurology 1980, 30: 263-271.","journal-title":"Neurology"},{"key":"ref_9","first-page":"247","volume":"30","author":"Cumming, W.J.K.; Hardy, M.; Hudgson, P.","year":"1976","unstructured":"Cumming, W.J.K., Hardy, M., Hudgson, P. et al. Carnitine palmityl transferase deficiency. J Neurol Sci 1976, 30: 247-258.","journal-title":"et al. Carnitine palmityl transferase deficiency. J Neurol Sci"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"929","DOI":"10.1126\/science.182.4115.929","article-title":"Muscle carnitine palmityltransferase deficiency and myoglobinuria","volume":"182","author":"DiMauro, S.; DiMauro, P.M.M.","year":"1973","unstructured":"DiMauro, S. & DiMauro, P.M.M. Muscle carnitine palmityltransferase deficiency and myoglobinuria. Science 1973, 182: 929-931.","journal-title":"Science"},{"key":"ref_11","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1056\/NEJM197502272920902","article-title":"A disorder of muscle lipid metabolism and myoglobinuria - absence of carnitine palmityltransferase","volume":"292","author":"Bank, W.J.; DiMauro, S.; Bonila, E.","year":"1975","unstructured":"Bank, W.J., DiMauro, S., Bonila, E. et al. A disorder of muscle lipid metabolism and myoglobinuria - absence of carnitine palmityltransferase. N Engl J Med 1975, 292: 443-449.","journal-title":"N Engl J Med"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"553","DOI":"10.1056\/NEJM197803092981007","article-title":"Partial deficiency of muscle carnitine palmityltransferase with normal ketone production","volume":"298","author":"Hosteller, K.Y.; Hoppel, C.L.; Romine, J.S.","year":"1978","unstructured":"Hosteller, K.Y., Hoppel, C.L., Romine, J.S. et al. Partial deficiency of muscle carnitine palmityltransferase with normal ketone production. N Engl J Med 1978, 298: 553-557.","journal-title":"N Engl J Med"},{"key":"ref_13","doi-asserted-by":"crossref","first-page":"679","DOI":"10.1136\/jnnp.43.8.679","article-title":"Combined partial deficiency of muscle carnitine palmityltransferase and carnitine with autosomal dominant inheritance","volume":"43","author":"Ionasescu, V.; Hug, G.; Hoppel, C.","year":"1980","unstructured":"Ionasescu, V., Hug, G. & Hoppel, C. Combined partial deficiency of muscle carnitine palmityltransferase and carnitine with autosomal dominant inheritance. J Neurol Neurosurg Psychiatry 1980, 43: 679-682.","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"ref_14","doi-asserted-by":"crossref","first-page":"883","DOI":"10.1212\/WNL.31.7.883","article-title":"Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritance","volume":"31","author":"Angelina, C.; Freddo, L.; Battistella, P.","year":"1981","unstructured":"Angelina, C., Freddo, L. & Battistella, P. Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritance. Neurology 1981, 31: 883-886.","journal-title":"Neurology"}],"container-title":["Postgraduate Medical Journal"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/academic.oup.com\/pmj\/article-pdf\/66\/773\/235\/50077172\/postgradmedj-66-235.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/academic.oup.com\/pmj\/article-pdf\/66\/773\/235\/50077172\/postgradmedj-66-235.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,4,28]],"date-time":"2023-04-28T15:33:21Z","timestamp":1682696001000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/pmj\/article\/66\/773\/235\/7062074"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1990,3,1]]},"references-count":14,"journal-issue":{"issue":"773","published-online":{"date-parts":[[1990,3,1]]},"published-print":{"date-parts":[[1990,3,1]]}},"URL":"https:\/\/doi.org\/10.1136\/pgmj.66.773.235","relation":{},"ISSN":["0032-5473","1469-0756"],"issn-type":[{"value":"0032-5473","type":"print"},{"value":"1469-0756","type":"electronic"}],"subject":[],"published-other":{"date-parts":[[1990,3]]},"published":{"date-parts":[[1990,3,1]]}}}