{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,2]],"date-time":"2023-10-02T07:20:14Z","timestamp":1696231214774},"reference-count":21,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2015,10,28]],"date-time":"2015-10-28T00:00:00Z","timestamp":1445990400000},"content-version":"vor","delay-in-days":27,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatrics International"],"published-print":{"date-parts":[[2015,10]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>A 7\u2010year\u2010old girl had been followed up for persistent conjugated hyperbilirubinemia since birth. Alanine aminotransferase, aspartate aminotransferase and \u03b3\u2010glutamyl transpeptidase activity was within the normal range, and liver protein synthesis had always been normal. Infectious etiology of jaundice, autoimmune diseases, drug\u2010induced liver injury, hemolytic anemia, \u03b1\u20101 anti\u2010trypsin deficiency, Wilson disease and Gilbert syndrome were ruled out. At the age of 8\u2009years the patient underwent radionuclide dynamic cholescintigraphy, indicating poor accumulation of the radiotracer in the liver on one hand, and severe retention of the radiopharmaceutical in the blood pool (including the heart) on the other hand. Rotor syndrome was suspected and finally confirmed on molecular analysis. This case represents the first cholescintigraphy report in a pediatric patient with genetically proven Rotor syndrome.<\/jats:p>","DOI":"10.1111\/ped.12676","type":"journal-article","created":{"date-parts":[[2015,10,28]],"date-time":"2015-10-28T08:19:53Z","timestamp":1446020393000},"page":"981-985","source":"Crossref","is-referenced-by-count":1,"title":["Radionuclide cholescintigraphy in genetically confirmed Rotor syndrome"],"prefix":"10.1111","volume":"57","author":[{"given":"Pavel","family":"Sirucek","sequence":"first","affiliation":[{"name":"Faculty Hospital and Faculty of Medicine  Ostrava"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Astrida","family":"Sulakova","sequence":"additional","affiliation":[{"name":"Faculty Hospital and Faculty of Medicine  Ostrava"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Milan","family":"Jirsa","sequence":"additional","affiliation":[{"name":"Institute for Clinical and Experimental Medicine  Prague Czech Republic"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lubomir","family":"Mrhac","sequence":"additional","affiliation":[{"name":"Faculty Hospital and Faculty of Medicine  Ostrava"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Martin","family":"Havel","sequence":"additional","affiliation":[{"name":"Faculty Hospital and Faculty of Medicine  Ostrava"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Otakar","family":"Kraft","sequence":"additional","affiliation":[{"name":"Faculty Hospital and Faculty of Medicine  Ostrava"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2015,10,28]]},"reference":[{"key":"e_1_2_5_2_1","first-page":"500","article-title":"Dubin\u2010Johnson syndrome: A clinicopathologic study of twenty cases","volume":"49","author":"Rastogi A","year":"2006","journal-title":"Indian J. 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