Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,003,237 papers from all fields of science
Search
Sign In
Create Free Account
Biliary Atresia
Known as:
Biliary atresia, congenital
, EHBA
, Biliary duct atresia
Expand
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
Create Alert
Alert
Related topics
Related topics
24 relations
Broader (5)
Atresia
Cholestasis
Congenital Disorders
Fetal Diseases
Expand
Bile duct proliferation
Bile duct structure
Biliary tract structure
Cat eye syndrome
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Impact of Age at Kasai Operation on Its Results in Late Childhood and Adolescence: A Rational Basis for Biliary Atresia Screening
Marie-Odile Serinet
,
B. Wildhaber
,
+5 authors
C. Chardot
Pediatrics
2009
Corpus ID: 26044814
BACKGROUND. Increased age at surgery has a negative impact on results of the Kasai operation for biliary atresia in infancy and…
Expand
Review
2006
Review
2006
Two Hundred Forty Consecutive Portal Vein Embolizations Before Extended Hepatectomy for Biliary Cancer: Surgical Outcome and Long-term Follow-Up
M. Nagino
,
J. Kamiya
,
H. Nishio
,
T. Ebata
,
T. Arai
,
Y. Nimura
Annals of Surgery
2006
Corpus ID: 36597113
Objective:To assess clinical benefit of portal vein embolization (PVE) before extended, complex hepatectomy for biliary cancer…
Expand
Highly Cited
2005
Highly Cited
2005
Outcome in adulthood of biliary atresia: A study of 63 patients who survived for over 20 years with their native liver
P. Lykavieris
,
C. Chardot
,
M. Sokhn
,
F. Gauthier
,
J. Valayer
,
O. Bernard
Hepatology
2005
Corpus ID: 32488464
To define the long‐term prognosis of children undergoing the Kasai operation for biliary atresia, a retrospective study was…
Expand
Highly Cited
2004
Highly Cited
2004
The murine winged-helix transcription factor Foxl2 is required for granulosa cell differentiation and ovary maintenance
D. Schmidt
,
C. Ovitt
,
+4 authors
M. Treier
Development
2004
Corpus ID: 31658647
Human Blepharophimosis/ptosis/epicanthus inversus syndrome (BPES) type I is an autosomal dominant disorder associated with…
Expand
Review
2003
Review
2003
Pathogenesis and outcome of biliary atresia: current concepts.
R. Sokol
,
C. Mack
,
M. Narkewicz
,
F. Karrer
Journal of Pediatric Gastroenterology and…
2003
Corpus ID: 17672661
Neonatal cholestatic disorders are a group of hepatobiliary diseases occurring within the first 3 months of life. Bile flow is…
Expand
Highly Cited
2002
Highly Cited
2002
Hepatic and extrahepatic malignancies in primary sclerosing cholangitis.
A. Bergquist
,
A. Ekbom
,
+10 authors
U. Broomé
Journal of Hepatology
2002
Corpus ID: 20374275
Highly Cited
1993
Highly Cited
1993
Biliary atresia splenic malformation syndrome: an etiologic and prognostic subgroup.
M. Davenport
,
M. Savage
,
A. Mowat
,
E. Howard
Surgery
1993
Corpus ID: 45385448
BACKGROUND The polysplenia syndrome is the most common extrahepatic anomaly found in association with extrahepatic biliary…
Expand
Highly Cited
1985
Highly Cited
1985
Biliary atresia.
R. Altman
,
J. Levy
Pediatric annals
1985
Corpus ID: 1814629
Highly Cited
1985
Highly Cited
1985
Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis.
C. Niederau
,
R. Fischer
,
A. Sonnenberg
,
W. Stremmel
,
H. Trampisch
,
G. Strohmeyer
New England Journal of Medicine
1985
Corpus ID: 42306344
We analyzed survival and causes of death among 163 patients with primary hemochromatosis diagnosed between 1959 and 1983. The…
Expand
Highly Cited
1955
Highly Cited
1955
Congenital intestinal atresia; observations on its origin.
J. Louw
,
C. Barnard
The Lancet
1955
Corpus ID: 40596726
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE