Allospecificity of liver allograft-derived lymphocytes and correlation with clinicopathologic findings [PDF]
Demetris, AJ +6 more
core
ABSTRACT Background Left‐sided hepatectomy for perihilar cholangiocarcinoma includes conventional left hepatectomy (C‐LH; H1234‐B), extended left hepatectomy (E‐LH; H12345′8′‐B‐MHV), and left trisectionectomy (LT; H123458‐B). The anatomical characteristics of the resected length of the right hepatic duct (RHD) in E‐LH remain unclear.
Kota Sugiura +9 more
wiley +1 more source
The Frequency of Anatomical Variants of the Bile Ducts: A Review Based on a Single Classification as Support for Cholangiographic Examinations. [PDF]
Olmedo NB, Dos Santos JS, Junior JE.
europepmc +1 more source
Iatrogenic bile duct stricture
G W Johnston, P G Reasbeck, L F Tinckler
openaire +2 more sources
Papillary Neoplasms of the Gallbladder and Extrahepatic Bile Ducts: A Report of Two Cases With Associated Invasive Carcinoma. [PDF]
Miry N +4 more
europepmc +1 more source
Abstract Objectives To investigate the prognostic significance of aspartate aminotransferase to platelet ratio index (APRI) in relation to histopathological features across the clinical course of biliary atresia (BA). Methods In this observational cohort study, we enrolled 135 BA patients with available APRI values at Kasai portoenterostomy (KPE, n ...
Nicholas Nordenheim +7 more
wiley +1 more source
Serum predictors of native liver survival post‐Kasai: Systematic review and meta‐analysis
Abstract Objectives After hepatoportoenterostomy (HPE), a minority of biliary atresia (BA) patients reach adolescence without liver transplantation. Several serum markers have been suggested to better predict post‐HPE outcomes in BA patients. We aimed to identify serum predictors of native liver survival (NLS) in post‐HPE BA patients.
Ahmad Anouti +5 more
wiley +1 more source
Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea
Abstract Among congenital diarrhea and enteropathies (CODEs), proprotein convertase subtilisin/kexin type 1 (PCSK1) deficiency is a rare monogenic disorder, associated with severe neonatal diarrhea and polyendocrinopathies. We report an 18‐day‐old male neonate, born to consanguineous parents, presenting with persistent watery diarrhea, metabolic ...
Eleonora Saraceno +7 more
wiley +1 more source
Complex Reconstruction of Right-Lobe Grafts on the Bench: Portal Vein, Anterior Sector Hepatic Veins, Inferior Hepatic Veins and Multiple Bile Ducts. [PDF]
Gupta AA, Soin AS.
europepmc +1 more source

