- ►clinchem.org DR Dufour, JA Lott, FS Nolte, DR Gretch, RS Koff … - Clinical …, 2000 - Am Assoc Clin Chem 1 Pathology and Laboratory Medicine Service, Veterans Affairs Medical Center, Washington,
DC 20422, and Department of Pathology, George Washington University School of
Medicine, Washington, DC 20037. ... 2 Department of Pathology, The Ohio State ... Cited by 167 - Related articles - BL Direct - All 14 versions
CN Van der Veere, M Sinaasappel, AF McDonagh, … - Hepatology, 1996 - interscience.wiley.com This study represents a multicenter survey on the management of patients with Crigler-Najjar
syndrome (CNS) type 1. The aim of the survey was to find guiding principles for physicians in
the care of these patients. Fifty-seven patients were included. At the time of inclusion, 21 ... Cited by 68 - Related articles - BL Direct - All 4 versions
PLM Jansen - European Journal of Pediatrics, 1999 - Springer Abstract Crigler-Najjar syndrome (CNS) results from a mutation in one of the Ūve exons of the
gene coding for the enzyme bilirubin-UDP-glucuronosyltransferase by exon 1*1 and exons 2ą5
of the UDP-glucuronosyltransferase 1 locus, the bilirubin glucuronidating isoform of UDP- ... Cited by 58 - Related articles - BL Direct - All 4 versions
T te Boekhorst, M Urlus, W Doesburg, SH Yap, RJA … - Journal of hepatology, 1988 - Elsevier In order to understand the pathophysiology of jaundice in severely ill patients, we have examined
several possible promoting factors in a retrospective study of 86 patients with multiple organ
failure admitted to an intensive care unit (ICU). Patients with bile duct obstruction were ... Cited by 28 - Related articles - All 4 versions
M Persico, E Persico, CT Bakker, I Rigato, A … - Hepatology, 2001 - interscience.wiley.com Although in Gilbert's syndrome (GS), bilirubin glucuronidation is impaired due to an extra TA
in the TATA box of the promoter of the gene for bilirubin UDP-glucuronosyltransferase 1
(UGT1A1), many GS homozygotes lack unconjugated hyperbilirubinemia. Accordingly, an ... Cited by 27 - Related articles - BL Direct - All 3 versions
- ►clinchem.org [PDF] D Pirulli, M Giordano, D Puzzer, S Crovella, I … - Clinical …, 2000 - Am Assoc Clin Chem The scavenger receptor class B type 1 (SR-BI), a multili- gand receptor, appears to be a physiologically
relevant HDL receptor in rodents (1, 2). To determine its role in humans, the human SRB1 gene
has been characterized (3, 4) and its genetic variation investigated in a Caucasian ... Cited by 24 - Related articles - BL Direct - All 4 versions
CL Mack, FA Zelko, J Lokar, R Superina, EM Alonso, … - Pediatrics, 2006 - Am Acad Pediatrics OBJECTIVES. Children with primary extrahepatic portal vein thrombosis (EHPVT) have
portal-systemic shunting, which may lead to disturbed neurocognitive function similar to
portal-systemic encephalopathy (PSE) seen with chronic liver disease and cirrhosis. The ... Cited by 17 - Related articles - BL Direct - All 5 versions
- ►rug.nl [PDF] T Nishioka, AM Hafkamp, R Havinga, PPE van Lierop … - The Journal of pediatrics, 2003 - Elsevier Orlistat treatment decreased plasma UCB concentrations (at 3 weeks; 100 mg/kg,
−33%±8%, P<.05; 200 mg/kg, −46%±10%, P<.01). Within days of treatment, orlistat treatment
increased fecal excretion of UCB (at day 3; +220%, P<.05). During 24 weeks of orlistat ... Cited by 14 - Related articles - All 15 versions
PLM Jansen - Journal of hepatology, 1996 - Elsevier Journal of Hepatology 1996; 25: 398404 Printed in Denmark All rights reserved Munksgaard
Copenhagen Copyright European Association for the Study of the Liver 1996 Journal of Hepatology
ISSN 0168.8278 Review Genetic diseases of bilirubin metabolism: the inherited ... Cited by 12 - Related articles - BL Direct - All 5 versions
