Publisher Copyright: © 2021 The Author(s)Portoenterostomy (PE) has remained as the generally accepted first line surgical treatment for biliary atresia (BA) for over 50 years. Currently, close to half of BA patients survive beyond 10 years with their native livers, and most of them reach adulthood without liver transplantation (LT). Despite normalization of serum bilirubin by PE, ductular reaction and portal fibrosis persist in the native liver. The chronic cholangiopathy progresses to cirrhosis, complications of portal hypertension, recurrent cholangitis or hepatobiliary tumors necessitating LT later in life. Other common related health problems include impaired bone health, neuromotor development and quality of life. Only few high-quality...
ObjectivesTo examine the medical status of children with biliary atresia (BA) with their native live...
OBJECTIVES: To determine the prognosis of patients with biliary atresia (BA) after two years of nati...
BACKGROUND & AIMS: Surgical treatment with Kasai portoenterostomy has improved the prognosis for...
Publisher Copyright: © 2021 The Author(s)Portoenterostomy (PE) has remained as the generally accepte...
Background/purpose: Biliary atresia is the most common reason for newborn cholestasis and pediatric ...
BACKGROUND: Different treatment policies can influence biliary atresia outcomes, but the pathophysio...
Biliary atresia (BA) is a rare disease of infancy in which obliteration of the biliary tract results...
Background: Progression of fibrosis and ensuing complications determine the postoperative course of ...
Item does not contain fulltextBACKGROUND: Biliary atresia is a progressive biliary injury which occu...
Background/purpose: Biliary atresia is the most common reason for newborn cholestasis and pediatric ...
Introduction: Biliary atresia (BA) represents the leading indication for liver transplantation in ch...
Item does not contain fulltextBACKGROUND & AIMS: Surgical treatment with Kasai portoenterostomy has ...
Biliary atresia (BA) is a rare neonatal cholestatic disease of unknown etiology and is the commonest...
We investigated noninvasive follow-up markers for histologic liver fibrosis and portal hypertension ...
OBJECTIVES: To determine the prognosis of patients with biliary atresia (BA) after two years of nati...
ObjectivesTo examine the medical status of children with biliary atresia (BA) with their native live...
OBJECTIVES: To determine the prognosis of patients with biliary atresia (BA) after two years of nati...
BACKGROUND & AIMS: Surgical treatment with Kasai portoenterostomy has improved the prognosis for...
Publisher Copyright: © 2021 The Author(s)Portoenterostomy (PE) has remained as the generally accepte...
Background/purpose: Biliary atresia is the most common reason for newborn cholestasis and pediatric ...
BACKGROUND: Different treatment policies can influence biliary atresia outcomes, but the pathophysio...
Biliary atresia (BA) is a rare disease of infancy in which obliteration of the biliary tract results...
Background: Progression of fibrosis and ensuing complications determine the postoperative course of ...
Item does not contain fulltextBACKGROUND: Biliary atresia is a progressive biliary injury which occu...
Background/purpose: Biliary atresia is the most common reason for newborn cholestasis and pediatric ...
Introduction: Biliary atresia (BA) represents the leading indication for liver transplantation in ch...
Item does not contain fulltextBACKGROUND & AIMS: Surgical treatment with Kasai portoenterostomy has ...
Biliary atresia (BA) is a rare neonatal cholestatic disease of unknown etiology and is the commonest...
We investigated noninvasive follow-up markers for histologic liver fibrosis and portal hypertension ...
OBJECTIVES: To determine the prognosis of patients with biliary atresia (BA) after two years of nati...
ObjectivesTo examine the medical status of children with biliary atresia (BA) with their native live...
OBJECTIVES: To determine the prognosis of patients with biliary atresia (BA) after two years of nati...
BACKGROUND & AIMS: Surgical treatment with Kasai portoenterostomy has improved the prognosis for...