Results 201 to 210 of about 196,612 (310)

Differences in Right Hepatic Duct Length Among Left‐Sided Hepatectomies: Conventional Hepatectomy Versus Extended Hepatectomy Versus Trisectionectomy

open access: yesJournal of Hepato-Biliary-Pancreatic Sciences, EarlyView.
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

Iatrogenic bile duct stricture

open access: yesJournal of British Surgery, 1986
G W Johnston, P G Reasbeck, L F Tinckler
openaire   +2 more sources

The changing face of hepatic resection [PDF]

open access: yes, 1989
Iwatsuki, S, Sheahan, DG, Starzl, TE
core   +1 more source

Serum aspartate aminotransferase to platelet ratio index in relation to liver histopathology of biliary atresia

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
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]

open access: yesCureus
Mujakovic E   +9 more
europepmc   +1 more source

Serum predictors of native liver survival post‐Kasai: Systematic review and meta‐analysis

open access: yesJournal of Pediatric Gastroenterology and Nutrition, EarlyView.
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

open access: yesJPGN Reports, EarlyView.
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

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