Results 191 to 200 of about 15,869 (231)
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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 ...
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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 ...
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Biliary atresia and biliary cysts
Baillière's Clinical Gastroenterology, 1997The 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.
P A, Lipsett, D L, Segev, P M, Colombani
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Journal of Pediatric Gastroenterology and Nutrition, 2015
ABSTRACTBiliary atresia is a rare disease of unclear etiology, in which obstruction of the biliary tree causes severe cholestasis leading to cirrhosis and ultimately death if left untreated. Biliary atresia is the leading cause of neonatal cholestasis and the most frequent indication for pediatric liver transplantation.
Amy G, Feldman, Cara L, Mack
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ABSTRACTBiliary atresia is a rare disease of unclear etiology, in which obstruction of the biliary tree causes severe cholestasis leading to cirrhosis and ultimately death if left untreated. Biliary atresia is the leading cause of neonatal cholestasis and the most frequent indication for pediatric liver transplantation.
Amy G, Feldman, Cara L, Mack
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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 ...
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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 ...
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Current Opinion in Gastroenterology, 1979
This chapter discusses the causes and management of extrahepatic biliary atresia. Extrahepatic biliary atresia, the most common of the progressive hepatic disorders, is itself a rare disease affecting approximately 1: 14,000 live-born infants. It is, nevertheless, the most important hepatic cause of morbidity in infancy and early childhood.
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This chapter discusses the causes and management of extrahepatic biliary atresia. Extrahepatic biliary atresia, the most common of the progressive hepatic disorders, is itself a rare disease affecting approximately 1: 14,000 live-born infants. It is, nevertheless, the most important hepatic cause of morbidity in infancy and early childhood.
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Pediatric and Developmental Pathology, 2004
Extrahepatic biliary atresia (EHBA) is an inflammatory fibrosing process affecting the extrahepatic and intrahepatic biliary tree resulting in fibrous obliteration of the extrahepatic biliary tract, ductopenia of intrahepatic bile ducts, and biliary cirrhosis.
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Extrahepatic biliary atresia (EHBA) is an inflammatory fibrosing process affecting the extrahepatic and intrahepatic biliary tree resulting in fibrous obliteration of the extrahepatic biliary tract, ductopenia of intrahepatic bile ducts, and biliary cirrhosis.
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Hepatology, 1984
Extrahepatic biliary atresia is defined as partial or total absence of permeable bile duct between porta hepatis and the duodenum. The incidence varies from 1:8,000 to 1:10,000. Cholestasis is total and permanent. 131I Rose Bengal test and needle liver biopsy allow correct identification of 95% of cases before surgery Before ...
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Extrahepatic biliary atresia is defined as partial or total absence of permeable bile duct between porta hepatis and the duodenum. The incidence varies from 1:8,000 to 1:10,000. Cholestasis is total and permanent. 131I Rose Bengal test and needle liver biopsy allow correct identification of 95% of cases before surgery Before ...
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Pediatrics, 1981
Since Kasai et al1 demonstrated convincingly that biliary atresia was a treatable, and in some instances curable condition, the approach to the jaundiced infant has changed dramatically. Efforts to identify infants with this disease were greatly accelerated as the "hands off" philosophy, predicated on the assumption that attempts to correct biliary ...
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Since Kasai et al1 demonstrated convincingly that biliary atresia was a treatable, and in some instances curable condition, the approach to the jaundiced infant has changed dramatically. Efforts to identify infants with this disease were greatly accelerated as the "hands off" philosophy, predicated on the assumption that attempts to correct biliary ...
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2023
Abstract Neonatal cholestasis syndrome includes a wide spectrum of diseases with varying clinical phenotypes all of which present with cholestasis in infancy. Biliary atresia is one of the causes of cholestasis and mandates early diagnosis and corrective surgery.
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Abstract Neonatal cholestasis syndrome includes a wide spectrum of diseases with varying clinical phenotypes all of which present with cholestasis in infancy. Biliary atresia is one of the causes of cholestasis and mandates early diagnosis and corrective surgery.
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