<p>Gilbert’s syndrome is a common genetic disease caused by deficiency of the liver enzyme UDP-glucuronyl transferase. The objective of the investigation is to study pathology of different portions of the gastrointestinal tract in children with Gilbert’s syndrome. A total of 182 children aged 3 to 17 years with Gilbert’s syndrome, who had been admitted to the clinic with the signs of jaundice and different gastroenterological complaints and symptoms, were examined. According to comprehensive examination results, among the gastrointestinal diseases in the patients, there was a preponderance duodenal injuries (41,5% of all diagnoses), there were less common injuries of the stomach (23,7%), esophagus (20%), and large bowel (14,8%). There was a...
Relevance. Gilbert’s syndrome (GS) is a disease with an autosomal recessive type of inheritance caus...
Hereditary spherocytosis is the most frequent congenital hemolytic anemia and is characterized with ...
AbstractIn our mutation analyses of bilirubin UDP glycosyltransferase (UGT1A1) gene, we encountered ...
Gilbert’s syndrome is a benign indirect hyperbilirubinemia of the hereditary nature, caused by defic...
Introduction: Jaundice is a common condition during the neonatal period. Prolonged jaundice occurs i...
Gilbert\'s syndrome (GS) is a benign condition that does not progress to chronic liver disease or fi...
Background and Aim: The pathogenesis of neonatal hyperbilirubinemia hasn't been completely defined i...
Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. It is character...
Gilbert syndrome is benign, often familial condition characterized by recurrent but asymptomatic mil...
BACKGROUND: Gilbert syndrome as a rule becomes manifest in adolescence or in early adulthood; it may...
Abstract Background Gilbert syndrome (GS) is an autosomal recessive inherited disorder of bilirubin ...
AbstractBackgroundGaucher’s disease (GD) is an autosomal recessive genetic disorder that results fro...
The role of Gilbert's syndrome (GS) in neonatal hyper-bilirubinemia, characterized by bilirubin leve...
BACKGROUND/AIMS: UDP-glucuronosyltransferases (UGTs) are important enzymes involved in glucuronidati...
Gilbert syndrome (GS) is characterized by intermittent unconjugated hyperbilirubinemia without struc...
Relevance. Gilbert’s syndrome (GS) is a disease with an autosomal recessive type of inheritance caus...
Hereditary spherocytosis is the most frequent congenital hemolytic anemia and is characterized with ...
AbstractIn our mutation analyses of bilirubin UDP glycosyltransferase (UGT1A1) gene, we encountered ...
Gilbert’s syndrome is a benign indirect hyperbilirubinemia of the hereditary nature, caused by defic...
Introduction: Jaundice is a common condition during the neonatal period. Prolonged jaundice occurs i...
Gilbert\'s syndrome (GS) is a benign condition that does not progress to chronic liver disease or fi...
Background and Aim: The pathogenesis of neonatal hyperbilirubinemia hasn't been completely defined i...
Gilbert syndrome is the most common inherited disorder of bilirubin glucuronidation. It is character...
Gilbert syndrome is benign, often familial condition characterized by recurrent but asymptomatic mil...
BACKGROUND: Gilbert syndrome as a rule becomes manifest in adolescence or in early adulthood; it may...
Abstract Background Gilbert syndrome (GS) is an autosomal recessive inherited disorder of bilirubin ...
AbstractBackgroundGaucher’s disease (GD) is an autosomal recessive genetic disorder that results fro...
The role of Gilbert's syndrome (GS) in neonatal hyper-bilirubinemia, characterized by bilirubin leve...
BACKGROUND/AIMS: UDP-glucuronosyltransferases (UGTs) are important enzymes involved in glucuronidati...
Gilbert syndrome (GS) is characterized by intermittent unconjugated hyperbilirubinemia without struc...
Relevance. Gilbert’s syndrome (GS) is a disease with an autosomal recessive type of inheritance caus...
Hereditary spherocytosis is the most frequent congenital hemolytic anemia and is characterized with ...
AbstractIn our mutation analyses of bilirubin UDP glycosyltransferase (UGT1A1) gene, we encountered ...