Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome)
about
Inherited disorders of bilirubin clearanceBilirubin in coronary artery disease: Cytotoxic or protective?Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liverTriclosan impairs excitation-contraction coupling and Ca2+ dynamics in striated muscleNEW INSIGHTS INTO THE PRESENCE OF BILIRUBIN IN A PLANT SPECIES STRELITZIA NICOLAI (STRELITZIACEAE).PPARα: A Master Regulator of Bilirubin HomeostasisPharmacogenomics of drug-metabolizing enzymes: a recent update on clinical implications and endogenous effects.The SLCO (former SLC21) superfamily of transporters.Intracytoplasmic crystalline inclusions in the hepatocytes of an antelope.Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis.General anesthesia in a patient with Gilbert's syndromePerinatal gene transfer to the liver.External validation of the bilirubin-atazanavir nomogram for assessment of atazanavir plasma exposure in HIV-1-infected patients.Multicenter phase II clinical trial of nilotinib for patients with imatinib-resistant or -intolerant chronic myeloid leukemia from the East Japan CML study group evaluation of molecular response and the efficacy and safety of nilotinib.Gilbert syndrome.Gilbert syndrome: the UGT1A1*28 promoter polymorphism as a biomarker of multifactorial diseases and drug metabolism.Effect of drug transporter pharmacogenetics on cholestasis.Importance of Hepatic Transporters in Clinical Disposition of Drugs and Their Metabolites.Chronically elevated bilirubin protects from cardiac reperfusion injury in the male Gunn rat.Oncology Drug Dosing in Gilbert Syndrome Associated with UGT1A1: A Summary of the Literature.Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening.UGT1A1 gene mutation due to Crigler-Najjar syndrome in Iranian patients: identification of a novel mutation.Assessment of safety in hepatic resection for hepatocellular carcinoma focusing on indirect hyperbilirubinemia.Defective UGT1A1 causes hyperbilirubinemiaDefective UGT1A4 causes hyperbilirubinemiaSerum total bilirubin concentrations are inversely associated with total white blood cell counts in an adult population.Perioperative Anesthetic Management of Patients Having Liver Transplantation for Uncommon Conditions.A Case of Acquired Gilbert's Syndrome.
P2860
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P2860
Hyperbilirubinemia syndromes (Gilbert-Meulengracht, Crigler-Najjar, Dubin-Johnson, and Rotor syndrome)
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@ast
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@en
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@nl
type
label
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@ast
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@en
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@nl
prefLabel
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@ast
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@en
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@nl
P3181
P1476
Hyperbilirubinemia syndromes ( ...... n-Johnson, and Rotor syndrome)
@en
P2093
Christian P Strassburg
P304
P3181
P356
10.1016/J.BPG.2010.07.007
P407
P577
2010-10-01T00:00:00Z