International audienceObjectives Malnutrition is common in children with biliary atresia (BA) awaiting liver transplantation (LT). Few studies have evaluated the effectiveness of enteral nutrition (EN) in these patients. The objective of this work was to assess the efficacy and tolerance of EN in children with BA awaiting LT. Methods A total of 31 patients with BA followed between 1995 and 2018 were retrospectively included. Anthropometric indicators (weight, length, and head circumference) and adverse effects of EN were noted at the start (T0) and the end (T1) of EN. The z -scores for anthropometric indicators were compared between T0 and T1. Results The median age at T0 was 7 months (interquartile range [IQR] 5–9), and the median duration...
Biliary atresia (BA) is a congenital malformation or an evolutive inflammatory process which, withou...
PURPOSE: The purpose of this study was to assess the overall results of recipients undergoing transp...
The nutritional profiles of 37 children (aged 0.5-14.0 years) with chronic liver disease at the time...
International audienceObjectives Malnutrition is common in children with biliary atresia (BA) awaiti...
WOS: 000406275100011PubMed ID: 28699603Background/Aims: Biliary atresia (BA) is the main cause of ne...
Biliary atresia (BA) is a rare disease of infancy in which obliteration of the biliary tract results...
Malnutrition is a significant clinical problem in infants with biliary atresia. The natural history ...
Metabolic diseases (MD) are the second largest indication group for orthotopic liver transplantation...
Biliary atresia is the most frequent cause of chronic cholestasis in infants. When left untreated, t...
Abstract It is important to prevent protein/calorie malnutrition in children with end stage liver d...
The nutritional profiles of 37 children (aged 0.5-14.0 years) with chronic liver disease at the time...
OBJECTIVE: To analyze the nutritional status of pediatric patients after orthotopic liver transplant...
Objectives: Most infants with biliary atresia (BA) require liver transplantation (LT) after hepatopo...
SUMMARY Biliary atresia is the leading cause of chronic infantile cholestasis which eventually leads...
OBJECTIVE: To analyze the nutritional status of pediatric patients after orthotopic liver transplant...
Biliary atresia (BA) is a congenital malformation or an evolutive inflammatory process which, withou...
PURPOSE: The purpose of this study was to assess the overall results of recipients undergoing transp...
The nutritional profiles of 37 children (aged 0.5-14.0 years) with chronic liver disease at the time...
International audienceObjectives Malnutrition is common in children with biliary atresia (BA) awaiti...
WOS: 000406275100011PubMed ID: 28699603Background/Aims: Biliary atresia (BA) is the main cause of ne...
Biliary atresia (BA) is a rare disease of infancy in which obliteration of the biliary tract results...
Malnutrition is a significant clinical problem in infants with biliary atresia. The natural history ...
Metabolic diseases (MD) are the second largest indication group for orthotopic liver transplantation...
Biliary atresia is the most frequent cause of chronic cholestasis in infants. When left untreated, t...
Abstract It is important to prevent protein/calorie malnutrition in children with end stage liver d...
The nutritional profiles of 37 children (aged 0.5-14.0 years) with chronic liver disease at the time...
OBJECTIVE: To analyze the nutritional status of pediatric patients after orthotopic liver transplant...
Objectives: Most infants with biliary atresia (BA) require liver transplantation (LT) after hepatopo...
SUMMARY Biliary atresia is the leading cause of chronic infantile cholestasis which eventually leads...
OBJECTIVE: To analyze the nutritional status of pediatric patients after orthotopic liver transplant...
Biliary atresia (BA) is a congenital malformation or an evolutive inflammatory process which, withou...
PURPOSE: The purpose of this study was to assess the overall results of recipients undergoing transp...
The nutritional profiles of 37 children (aged 0.5-14.0 years) with chronic liver disease at the time...