Familial liver diseases

Factor II G 20210 a mutation in idiopathic portal vein thrombosis in children

Haemochromatosis gene mutations in chronic hepatitis C patients

Molecular biology in pediatric gastrointestinal and liver diseases

The value of human glutathione S-transferases in early detection of cystic fibrosis related liver disease

Glypican-3: A novel serum and histochemical marker for hepatocellular carcinoma

The role of glutathione -S- transferase gene mutation in the development of hepatocellular carcinoma

Metabolic liver diseases in infancy and childhood : Update in diagnosis and management

Cholestatic disorders of infancy : A detailed study of cases presenting during 2006 in the pediatric hepatology unit at Cairo University Children's Hospital

DNA sequencing of uncharacterized β–globin gene mutations in β–thalassaemia in children