Results 51 to 60 of about 15,869 (231)

Biliary atresia.

Mayo Clinic Proceedings, 1998
Extrahepatic biliary atresia is an obliterative cholangiopathy that involves all or part of the extrahepatic biliary tree and, in many cases, the intrahepatic bile ducts. In the United States, from 400 to 600 new cases of biliary atresia are encountered annually.
openaire   +2 more sources

Diagnosis and treatment of biliary atresia in children

Медицина болю, 2022
. There are relatively few severe liver diseases in childhood. Biliary atresia is one of the most difficult. Early diagnosis of this disease is the basis of the subsequent treatment algorithm.
K Dmytriieva, K Dmytriiev, M Vidiscak, V Vidiscak   +3 more
doaj   +1 more source

Beyond a Conduit: The Evolution of Functional Biliary Stents From Active Intervention to Enabling Platforms

iNew Medicine, EarlyView.
This review traces the evolution of functional biliary stents, outlining the paradigm shift from “active intervention” strategies that target stent failure to next‐generation “enabling platforms.” These platforms leverage biodegradable materials, 3D/4D printing, and smart sensors to achieve personalized, regenerative, and theranostic solutions ...
Muhan Li, Xu Liu, Xin Ye, Zhixia Dong, Xinjian Wan   +4 more
wiley   +1 more source

431 Galectin-3 as a Biomarker and Potential Therapeutic Target in Biliary Atresia [PDF]

, 2022
Dor Yoeli, Yuhuan Luo, Alexander Chaidez, Zhaohui Wang, Megan A. Adams, Christene A. Huang, Cara L. Mack, Nalu Navarro–Álvarez   +7 more
openalex   +1 more source

Hepatopulmonary syndrome in children and adolescents with portal hypertension in Brazil: A multicenter study

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives To describe the clinical and laboratory characteristics and outcomes of pediatric hepatopulmonary syndrome (HPS) secondary to portal hypertension (PH) in Brazil. Methods Fifty‐four pediatric patients diagnosed with PH and HPS according to the European Respiratory Society criteria were included in this multicenter retrospective study.
Leticia Drumond Alberto, Eleonora Druve Tavares Fagundes, Adriana Teixeira Rodrigues, Thaís Costa Nascentes Queiroz, Gustavo Valverde de Castro, Carlos Oscar Kieling, Sandra Maria Gonçalves Vieira, Natália Lamounier dos Martires Guerra, Natascha Silva Sandy, Gilda Porta, Irene Kazue Miura, Maria Ângela Bellomo Brandão, Gabriel Hessel, Adriana Maria Alves de Tommaso, Alexandre Rodrigues Ferreira   +14 more
wiley   +1 more source

Biliary atresia and situs inversus in infant: a rare case report [PDF]

Romanian Journal of Pediatrics
Background. Biliary atresia is the leading cause of liver transplantation in children. It is associated with other congenital anomalies. The presentation of biliary atresia with situs inversus is a rare case. Case presentation.
Rendi Aji Prihaningtyas, Seruni, Bagus Setyoboedi, Sjamsul Arief   +2 more
doaj   +1 more source

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

Journal 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 enroled 135 BA patients with available APRI values at Kasai portoenterostomy (KPE, n ...
Nicholas Nordenheim, Iiris Nyholm, Maria Hukkinen, Nelli Sjöblom, Aino Mutka, Jouko Lohi, Mark Davenport, Mikko P. Pakarinen   +7 more
wiley   +1 more source

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

Journal 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, Hamza Dahshi, Thomas G. Cotter, Tebyan A. Rabbani, Natasha Corbitt, Sara Hassan   +5 more
wiley   +1 more source

Vitamin B12 deficiency in a pediatric patient with gastric obstruction and jejunal feeding dependence: A case report

JPGN Reports, EarlyView.
Abstract Pediatric B12 deficiency is most caused by insufficient dietary intake, malabsorption or autoimmune gastritis. We present a unique case of B12 deficiency in a pediatric patient with complex gastrointestinal anatomy and jejunal nutritional dependence nearly two decades after unsuccessful surgical intervention.
Angela H. Nguyen, Dorsey Bass, Rachel E. Herdes   +2 more
wiley   +1 more source

Down-regulation of STAT3 enhanced chemokine expression and neutrophil recruitment in biliary atresia [PDF]

, 2021
Ming Fu, Ledong Tan, Zefeng Lin, Vincent Chi Hang Lui, Paul Tam, Jonathan R. Lamb, Yan Zhang, Huimin Xia, Ruizhong Zhang, Yan Chen   +9 more
openalex   +1 more source