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■ Abbreviation / Long Form : GS / Gilbert's syndrome

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Abbreviation:   GS  (>> Co-occurring Abbreviation)
Long Form:   Gilbert's syndrome
 Abbreviation Variation
 Long Form Variation
 Pair(Abbreviation/Long Form) Variation
No. Year Title Co-occurring Abbreviation
2019 The frequency, clinical course, and health related quality of life in adults with Gilbert's syndrome: a longitudinal study. CLDQ, SF-36v2
2018 "Gilbert's-like" syndrome as part of a spectrum of persistent unconjugated hyperbilirubinemia in post-chronic hepatitis patients. ---
2018 An Infant With Unusually High Unconjugated Hyperbilirubinemia Due to Coexistence of Hereditary Spherocytosis and Gilbert Syndrome. ---
2018 Bilirubin acts as a multipotent guardian of cardiovascular integrity: more than just a radical idea. ---
2018 Diagnostic criteria and contributors to Gilbert's syndrome. CVD
2018 Incidence and Risk of Gallstone Disease in Gilbert's Syndrome Patients in Indian Population. ---
2018 Induction of Mild Hyperbilirubinemia: Hype or Real Therapeutic Opportunity? UGT
2018 Mild hyperbilirubinaemia as an endogenous mitigator of overweight and obesity: Implications for improved metabolic health. CVD, FM, HC, UCB
2018 UGT1A1 (TA)n Promoter Genotype: Diagnostic and Population Pharmacogenetic Marker in Serbia. PCR
10  2018 UGT1A1 genotypes and unconjugated hyperbilirubinemia phenotypes in post-neonatal Chinese children: A retrospective analysis and quantitative correlation. CNS-I, CNS-II, OR, OR, PUCH, UCH
11  2018 [Study on spectrum of UGT1A1 mutations in connection with inherited non-hemolytic unconjugated hyperbilirubinemia]. ALT, AST, CNS-II, TB, UCB
12  2017 Anesthetic management of a case of Gilbert's syndrome for mitral and aortic valve replacement: Role of transesophageal echocardiography. CPB, HBF, TEE
13  2017 Characteristics of the heme catabolic pathway in mild unconjugated hyperbilirubinemia and their associations with inflammation and disease prevention. BLVRA, CRP, HO-1, HPT, HPX, SAA, UCB
14  2017 Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II. CNS-II
15  2017 Frequency of the UGT1A1*28 Polymorphism in a Romanian Cohort of Gilbert Syndrome Individuals. ---
16  2017 Genetic susceptibility to Gilbert's syndrome in a valencian population; efficacy of the fasting test. ---
17  2017 Gilbert syndrome in patients with type 1 diabetes-Prevalence, glycemic control, and microalbuminuria. IQR, T1DM
18  2017 Mildly elevated unconjugated bilirubin is associated with reduced platelet activation-related thrombogenesis and inflammation in Gilbert's syndrome. AA, ADP, CVD, UCB
19  2017 Oncology Drug Dosing in Gilbert Syndrome Associated with UGT1A1: A Summary of the Literature. ---
20  2017 The Association between Prolonged Jaundice and TATA Box Dinucleotide Repeats in Gilbert's Syndrome. PCR
21  2017 UGT1A1*28 relationship with abnormal total bilirubin levels in chronic hepatitis C patients: Outcomes from a case-control study. CHC, HCV, HIV, TB
22  2016 Features of an altered AMPK metabolic pathway in Gilbert's Syndrome, and its role in metabolic health. ---
23  2016 Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome. UDP
24  2016 Gilbert's syndrome in healthy blood donors what next?? ---
25  2016 Longer telomeres in chronic, moderate, unconjugated hyperbilirubinaemia: insights from a human study on Gilbert's Syndrome. BR, CVDs, UCB
26  2016 Relation between unconjugated bilirubin and RDW, neutrophil to lymphocyte ratio, platelet to lymphocyte ratio in Gilbert's syndrome. NLR, PLR, RDW, UCB
27  2015 Bilirubin, platelet activation and heart disease: a missing link to cardiovascular protection in Gilbert's syndrome? UCB, UGT1A1
28  2015 Evaluation of aortic stiffness in Gilbert syndrome patients: a protective effect of elevated bilirubin levels. HDL, IB, PWV
29  2015 GILBERT'S SYNDROME - A CONCEALED ADVERSITY FOR PHYSICIANS AND SURGEONS. ---
30  2015 Liver transplantation from living donors with Gilbert's syndrome is a safe procedure for both donors and recipients. LDLT, LT
31  2015 Outcome and toxicities associated to chemotherapy in children with acute lymphoblastic leukemia and Gilbert syndrome. Usefulness of UGT1A1 mutational screening. ALL
32  2015 Scoliosis in a Patient With Gilbert Syndrome: A Case Report and Review of the Literature. ---
33  2014 Correlation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome. BMJ, NH
34  2014 Perfluorocarbons and Gilbert syndrome (phenotype) in the C8 Health Study Population. PFCs, PFHxA
35  2014 Severe neonatal hyperbilirubinemia and UGT1A1 promoter polymorphism. ---
36  2014 Unconjugated bilirubin inhibits collagen induced platelet activation. CVD, UCB
37  2014 [Effect of anti-helicobacter therapy on the hepatic glucuronyl transferase system of adolescents with Gilbert's syndrome]. AHBT, GTF
38  2013 Bilirubin and beyond: a review of lipid status in Gilbert's syndrome and its relevance to cardiovascular disease protection. ---
39  2013 Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect. CNS, UGT
40  2013 Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database. CNS, STBC, UGT1A1
41  2013 Haem catabolism: a novel modulator of inflammation in Gilbert's syndrome. ---
42  2013 Protection from age-related increase in lipid biomarkers and inflammation contributes to cardiovascular protection in Gilbert's syndrome. LDL-C, SAA, UCB
43  2013 Short communication: fasting increases serum concentrations of bilirubin in patients receiving atazanavir: results from a pilot study. ---
44  2013 The effect of Gilbert's syndrome on the dispersions of QT interval and P-wave: an observational study. HR, Pd, QTd
45  2013 The evaluation of relationship between adiponectin levels and epicardial adipose tissue thickness with low cardiac risk in Gilbert`s syndrome: an observational study. APN, EAT
46  2013 [Prevalence of Gilbert syndrome and its genetic determinants in Chile]. TB
47  2013 [Ultrastructure of hepatocytes in Gilbert's syndrome patients and chronic hepatitis B patients]. CHB
48  2012 Acetaminophen administration in a patient with Gilbert's syndrome. ---
49  2012 Can an extended right lobe be harvested from a donor with Gilbert's syndrome for living-donor liver transplantation? Case report. LDLT
50  2012 Effects of unconjugated bilirubin on chromosomal damage in individuals with Gilbert's syndrome measured with the micronucleus cytome assay. BMCyt, CBMN, UCB
51  2012 Gilbert syndrome redefined: a complex genetic haplotype influences the regulation of glucuronidation. HBD, mRNA, SNPs
52  2012 Reduced circulating oxidized LDL is associated with hypocholesterolemia and enhanced thiol status in Gilbert syndrome. oxLDL
53  2012 Wayward effect of polymorphism (TA)8 in the promoter region of UGT1A1 gene in a Mexican family. UGT1A1
54  2011 Decreased small dense LDL levels in Gilbert's syndrome. BMI, hs-CRP, sdLDL-C
55  2011 Hereditary spherocytosis coexisting with UDP-glucuronosyltransferase deficiency highly suggestive of Crigler-Najjar syndrome type II. HS, UGT1A1
56  2011 Hyperbilirubinemia and intermittent lower urinary tract dysfunction. ---
57  2011 Prevalence of Gilbert syndrome in parents of neonates with pathologic indirect hyperbilirubinemia. ABO, G6PD, TSB
58  2010 A case of concomitant Gilbert's syndrome and hereditary spherocytosis. HS, TA
59  2009 Acute acalculous cholecystitis in children with Epstein-Barr virus infection: a role for Gilbert's syndrome? AAC, EBV
60  2009 Bone mineral densities in individuals with Gilbert's syndrome: a cross-sectional, case-control pilot study. BMD, PTH
61  2009 Soluble CD40 ligand and soluble P-selectin levels in Gilbert's syndrome: a link to protection against atherosclerosis? hs-CRP, sCD40L
62  2008 Decreased oxidation susceptibility of plasma low density lipoproteins in patients with Gilbert's syndrome. LDL
63  2008 Genotype frequencies of UDP-glucuronosyltransferase 1A1 promoter gene polymorphism in the population of healthy Croatian pre-scholars. B-UGT
64  2008 Gilbert syndrome, UGT1A1*28 allele, and cardiovascular disease risk: possible protective effects and therapeutic applications of bilirubin. CVD, HO
65  2008 Improved resistance to serum oxidation in Gilbert's syndrome: a mechanism for cardiovascular protection. CVD
66  2008 The inverse starving test is not a suitable provocation test for Gilbert's syndrome. UCB
67  2007 Combined UGT1A1 and UGT1A7 variant alleles are associated with increased risk of Gilbert's syndrome in Taiwanese adults. OR, UGT
68  2006 Gilbert's syndrome: an overview for clinical biochemists. ---
69  2006 Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene. CAT, UGT1A1
70  2006 Linkage disequilibrium of UGT1A1 *6 and UGT1A1 *28 in relation to UGT1A6 and UGT1A7 polymorphisms. LD, UGT
71  2006 Liver transplantation using donors with Gilbert syndrome. ---
72  2006 The role of Gilbert's syndrome and frequent NAT2 slow acetylation polymorphisms in the pharmacokinetics of retigabine. NAT2, PK, RA, RGB, SA
73  2006 UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis. UGT-1A1, UTIs
74  2006 [Gilbert's syndrome: a clinicogenetic trial]. ---
75  2005 Decreased levels of advanced glycation end-products in patients with Gilbert syndrome. AGEs, CML
76  2005 Gilbert's syndrome disclosed during the treatment of hematological malignancies. ---
77  2005 Proton magnetic resonance spectroscopy of the anterior cingulate gyrus, insular cortex and thalamus in schizophrenia associated with idiopathic unconjugated hyperbilirubinemia (Gilbert's syndrome). ---
78  2005 Role of overnight rifampin test in diagnosing Gilbert's syndrome. ---
79  2005 The role of UGT1A1*28 mutation in jaundiced infants with hypertrophic pyloric stenosis. HPS, IPS
80  2005 [Inherited disorders of bilirubin metabolism]. CDA 2, CN-1, HS, UGT
81  2004 Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects. CNS2, PCR
82  2004 Glucuronidation of acetaminophen is independent of UGT1A1 promotor genotype. ---
83  2002 A case of congenital dyserythropoietic anemia type II, Gilbert's syndrome and malleolar trophic ulcers. CDA-II
84  2002 Frequencies of UDP-glucuronosyltransferase 1 (UGT1A1) gene promoter polymorphisms among distinct ethnic groups from Brazil. UGT1A, UGT1A1
85  2002 Gilbert syndrome and ischemic heart disease: a protective effect of elevated bilirubin levels. HDL, IHD
86  2002 Neonatal hyperbilirubinemia and Gilbert's syndrome. ---
87  2002 Predicting the risk of sporadic elevated bilirubin levels and diagnosing Gilbert's syndrome by genotyping UGT1A1*28 promoter polymorphism. UGT1A1
88  2001 Gilbert syndrome associated with beta-thalassemia. ---
89  2001 Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1. UGT1A1
90  2001 Rifampicin test in the diagnosis of Gilbert's syndrome. ---
91  2001 [Refinement and role of the diagnosis of Gilbert disease with molecular biology]. ---
92  2000 Drug-mediated toxicity caused by genetic deficiency of UDP-glucuronosyltransferases. UGTs
93  2000 Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects. FRET, PCR
94  1999 Heterogeneity of paracetamol metabolism in Gilbert's syndrome. HPLC
95  1999 [The heterogeneity of paracetamol metabolism in Gilbert's disease]. HPLC, UGT
96  1998 Doxorubicin dosage guidelines in a patient with hyperbilirubinemia of Gilbert's syndrome. ---
97  1998 Gilbert syndrome accelerates development of neonatal jaundice. TA
98  1996 Gilbert syndrome. ---
99  1995 Caffeine clearance in subjects with constitutional unconjugated hyperbilirubinemia. CAF, ICG, SBA
100  1993 [Diagnostic porphyrinopathies in hereditary hyperbilirubinemia]. DJS, RS