Keywords: BA, biliary atresia; CI, confidence interval; OCS, observational clinical studies; OR, odds ratio; RCT, randomized controlled trialsBiliary atresia; Steroid; Kasai procedure; Pediatric; Jaundice clearance
مقالات ISI (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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Keywords: Cholestasis; Adaptive Immunity; Neonatal AutoimmunityAg, antigen; APC, antigen presenting cell; BA, biliary atresia; BCR, B-cell receptor; CD, cluster of differentiation; GST, glutathione S-transferase; IFN, interferon; IL, interleukin; NK, natural killer
Utility of CD127 combined with FOXP3 for identification of operational tolerance after liver transplantation
Keywords: ALT, alanine transaminase; APC, allophycocyanin; AST, aspartate transaminase; BA, biliary atresia; CBC, complete blood count; CD127dim cells, CD4+ CD25++ CD127dim cells; CD127dimFOXP3+ cells, CD4+ CD25++ CD127dimFOXP3+ cells; cpm, count per minute; CRP, C
Ultrasonography evaluation of infants with Alagille syndrome: In comparison with biliary atresia and neonatal hepatitis
Keywords: US, Ultrasonography; ALGS, Alagille syndrome; BA, Biliary atresia; NH, Neonatal hepatitis; GB, Gallbladder; TC, Triangular cord; OPC, Operative cholangiographyAlagille syndrome; Biliary atresia; Hepatitis; Ultrasonography; Gallbladder
APRi predicts native liver survival by reflecting portal fibrogenesis and hepatic neovascularization at the time of portoenterostomy in biliary atresia
Keywords: BA, biliary atresia; PE, portoenterostomy; APRi, aspartate aminotransferase-to-platelet ratio index; α-SMA, alpha smooth muscle actin; AST, serum aspartate aminotransferase; ALT, alanine aminotransferase; ALP, alkaline phosphatase; GT, gamma-glutamyl tran
Negative feedback loop of cholesterol regulation is impaired in the livers of patients with Alagille syndrome
Keywords: AGS, Alagille syndrome; BA, biliary atresia; TC, total cholesterol; TBA, total bile acids; LDLR, low-density lipoprotein receptor; HDL, high-density lipoprotein; SR-BI, scavenger receptor class B type I; HMGCR, 3-hydroxy-3-methylglutaryl coenzyme A reduct
Cytomegalovirus-associated biliary atresia: An aetiological and prognostic subgroup ★★★
Keywords: ALP, alkaline phosphatase; AST, aspartate aminotransferase; BA, biliary atresia; BASM, biliary atresia splenic malformation syndrome; CMV, cytomegalovirus; ELISA, enzyme-linked immunosorbent assay; GGT, γ-glutamyl transpeptidase; IgM, immunoglobulin M; KP
MicroRNA-21/PTEN/Akt axis in the fibrogenesis of biliary atresia
Keywords: miRNAs, microRNAs; miR-21, MicroRNA-21; BA, biliary atresia; PTEN, phosphatase and tensin homolog deleted on chromosome ten; a-SMA, a-smooth muscle actin; IHC, immunohistochemistry; HSC, hepatic stellate cell; MEM, minimum essential medium; H&E, hematoxyl
Genetic variability of interleukin4 gene in Taiwanese children with biliary atresia
Keywords: BA, biliary atresia; IL4, interleukin 4; BEC, biliary epithelial cells; SNP, single nucleotide polymorphisms; PCR, polymerase chain reactions; LD, linkage disequilibrium; ADCC, antibody-dependent cell-mediated cytotoxicity; FasL, Fas ligandsCholangiopathy
The biliary atresia splenic malformation syndrome: A 28-year single-center retrospective study
Keywords: BA, Biliary atresia; BASM, Biliary atresia splenic malformation; IVC, Inferior vena cava