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Biliary Atresia

Known as: Biliary atresia, congenital, EHBA, Biliary duct atresia 
Progressive destruction or the absence of all or part of the extrahepatic BILE DUCTS, resulting in the complete obstruction of BILE flow. Usually… Expand
National Institutes of Health

Papers overview

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Review
2009
Review
2009
Biliary atresia is a rare disease of infancy, which has changed within 30 years from being fatal to being a disorder for which… Expand
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Highly Cited
2009
Highly Cited
2009
BACKGROUND. Increased age at surgery has a negative impact on results of the Kasai operation for biliary atresia in infancy and… Expand
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Highly Cited
2006
Highly Cited
2006
OBJECTIVE To determine the prognostic factors and optimal approaches to the diagnosis and management of biliary atresia, the… Expand
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Highly Cited
2004
Highly Cited
2004
Human Blepharophimosis/ptosis/epicanthus inversus syndrome (BPES) type I is an autosomal dominant disorder associated with… Expand
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Highly Cited
2003
Highly Cited
2003
PURPOSE The aim of this study was to elucidate the epidemiology and short- and long-term results of biliary atresia in Japan… Expand
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Highly Cited
2002
Highly Cited
2002
BACKGROUND/AIMS To assess the risk of hepatic and extrahepatic malignancies in a large cohort of Swedish primary sclerosing… Expand
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Highly Cited
2000
Highly Cited
2000
BACKGROUND Biliary atresia is an obliterative cholangiopathy of infancy that is fatal if untreated. Surgical treatment, the Kasai… Expand
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Highly Cited
2000
Highly Cited
2000
ObjectiveTo determine the treatment efficacy, safety, local tumor control, and complications related to radiofrequency ablation… Expand
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Highly Cited
1985
Highly Cited
1985
 
Is this relevant?
Highly Cited
1985
Highly Cited
1985
We analyzed survival and causes of death among 163 patients with primary hemochromatosis diagnosed between 1959 and 1983. The… Expand
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