Children with biliary atresia show developmental problems, including language delays, following a living donor liver transplant (LDLT) in infancy…
Articles by Steve Bryson, PhD
A living donor liver transplant successfully managed liver failure in a 6-month-old boy with progressive familial intrahepatic cholestasis type 8…
Clinical genome sequencing, or cGS, testing to detect a rare genetic disease such as Alagille syndrome, resulted in a…
A team of researchers, backed by a grant totaling more than $3 million, will study the feasibility of a nationwide…
The U.S. Food and Drug Administration (FDA) has granted breakthrough therapy designation to larsucosterol, Durect’s investigational therapy for people…
One year of treatment with Gilead Sciences’ seladelpar normalized biomarkers of liver injury and rapidly reduced itch for most…
A reduced dose of soybean fat emulsion seems to be better than the standard dose at preventing parenteral nutrition-associated…
The blood levels of two proteins, called MMP-7 and SOX9, are significantly higher in infants with biliary atresia than…
April 19 is a day set aside to raise awareness of liver diseases such as Alagille syndrome. It’s…
Current screening and treatment strategies won’t allow Canada to eliminate new cases of hepatitis C by 2030, a population…