Results 271 to 280 of about 222,722 (307)
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Biliary atresia and biliary cysts

Baillière's Clinical Gastroenterology, 1997
The authors present a review of the classification, aetiology, presentation, treatment and long-term outcome of children and adults with biliary atresia and choledochal cyst disease. Biliary atresia should be suspected in any infant with jaundice beyond the second week of life.
Dorry L. Segev   +2 more
openaire   +3 more sources

Cardiac-associated biliary atresia (CABA): a prognostic subgroup

Archives of Disease in Childhood, 2020
Objectives To describe the range of concurrent cardiac malformations in biliary atresia (BA) while providing a functional framework of risk. Methods Demographic and variables were collected from a prospectively maintained single-centre database.
B. Aldeiri   +5 more
semanticscholar   +1 more source

Biliary atresia in the newborn

Journal of Pediatric Surgery, 1986
A prenatal sonographic diagnosis of extrahepatic biliary atresia was made and, 76 hours after birth, operatively confirmed. A standard Kasai operation was performed, with the exception of the use of an ancillary appendiceal conduit to provide biliary drainage of an independent bile duct draining the right anterior hepatic segment.
Roberta J. Hall   +3 more
openaire   +3 more sources

Etiopathogenesis of Biliary Atresia

Seminars in Liver Disease, 2001
Biliary atresia, a progressive sclerosis of the extrahepatic biliary tree that occurs only within the first 3 months of life, is one of the most common causes of neonatal cholestasis and accounts for over half of children who undergo liver transplantation.
Cara L. Mack, Ronald J. Sokol
openaire   +3 more sources

Genetics in biliary atresia

Current Opinion in Gastroenterology, 2019
Biliary atresia is a poorly understood deadly disease. Genetic predisposition factors are suspected albeit not firmly established. This review summarizes recent evidence of genetic alterations in biliary atresia.Whole-genome association studies in biliary atresia patients identified four distinct predisposition loci with four different genes ...
Muriel Girard, Ganna Panasyuk
openaire   +3 more sources

Biliary atresia

Pediatrics, 1975
It is difficult for me to find fault with Dr. Lilly's presentation, especially since he refers to me as a fair-minded, clear-thinking man! Dr. Thaler and I concluded in 1968 that the chance of encountering a patient with operable atresia of the extrahepatic biliary ducts was so small that our primary obligation was to protect the infant ...
openaire   +2 more sources

Congenital Biliary Atresia

Archives of Pediatrics & Adolescent Medicine, 1977
To the Editor.—It is somewhat puzzling to read the recent article on congenital biliary atresia in the August issue of theJournal(130:830,1976) by Kobayashi and co-workers and many others like it in recent literature. In theWestern Journal of Surgery, Obstetrics, and Gynecology(58:714, 1950) there is an article entitled "Surgical Relief of External ...
openaire   +3 more sources

Acquired biliary atresia

Journal of Pediatric Surgery, 1996
Three infants are described in whom acquired biliary atresia developed during the perinatal period. In two cases this was related to a spontaneous perforation of the bile duct, and in the other it probably was related to previous surgery for duodenal and ileal atresias.
Edward R. Howard   +2 more
openaire   +3 more sources

Serum MMP-7 in the Diagnosis of Biliary Atresia

Pediatrics, 2019
BA is a serious disorder with difficulty in accurate noninvasive diagnosis. This study validated the promising diagnostic accuracy of MMP-7 for BA.
Jingying Jiang   +7 more
semanticscholar   +1 more source

Biliary Atresia

Pediatrics In Review, 2022
Indira, Sriram, Daniel, Nicklas
openaire   +2 more sources

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