Results 201 to 210 of about 196,612 (310)
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
Double-balloon endoscopy-assisted bile duct biopsy with a long, tapered delivery system. [PDF]
Oka Y, Sakai A, Uza N, Kodama Y.
europepmc +1 more source
Iatrogenic bile duct stricture
G W Johnston, P G Reasbeck, L F Tinckler
openaire +2 more sources
The changing face of hepatic resection [PDF]
Iwatsuki, S, Sheahan, DG, Starzl, TE
core +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
Post-cholecystectomy Changes in the Common Bile Duct Diameter: A Comparative Ultrasound Study. [PDF]
Mujakovic E +9 more
europepmc +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
Application of enhanced recovery after surgery in laparoscopic biliary reoperation for extrahepatic bile duct stones. [PDF]
Lin C +5 more
europepmc +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

