Results 31 to 40 of about 226,924 (326)
Background: Biliary atresia (BA) is a progressive fibrosing obstructive cholangiopathy involving both the intrahepatic and extrahepatic biliary system; resulting in obstruction of bile flow and neonatal jaundice.
Ninung RD Kusumawati +5 more
doaj +1 more source
Biliatresone: progress in biliary atresia study
Background Biliary atresia (BA) is one of the main causes of neonatal end-stage liver disease. Without timely diagnosis and treatment, most children with BA will develop irreversible liver fibrosis within the first two months.
Jiajie Zhu +3 more
semanticscholar +1 more source
Biliary organoids uncover delayed epithelial development and barrier function in biliary atresia
Biliary atresia is a severe inflammatory and fibrosing cholangiopathy of neonates of unknown etiology. The onset of cholestasis at birth implies a prenatal onset of liver dysfunction.
S. Amarachintha +8 more
semanticscholar +1 more source
Value of the International Classification of Diseases code for identifying children with biliary atresia [PDF]
Background Although identifying cases in large administrative databases may aid future research studies, previous reports demonstrated that the use of the International Classification of Diseases, Tenth Revision (ICD-10) code alone for diagnosis leads to
Pornthep Tanpowpong +3 more
doaj +1 more source
Novel NIR-II fluorescent probes for biliary atresia imaging
Biliary atresia is a rare infant disease that predisposes patients to liver transplantation and death if not treated in time. However, early diagnosis is challenging because the clinical manifestations and laboratory tests of biliary atresia overlap with
Xiaodong Zeng +9 more
doaj +1 more source
It is still challenging to make accurate diagnosis of biliary atresia (BA) with sonographic gallbladder images particularly in rural area without relevant expertise.
Wenying Zhou +16 more
semanticscholar +1 more source
EP300/YAP1-SERPINE1 Signaling Regulates Ductular Reaction and Liver Fibrosis in Biliary Atresia. [PDF]
Zhu Z +9 more
europepmc +2 more sources
Abstract Patients with biliary atresia (BA) below 2 years of age in need of a transplantation largely rely on partial grafts from deceased donors (deceased donor liver transplantation [DDLT]) or living donors (living donor liver transplantation [LDLT]).
Hedayatullah Esmati +10 more
wiley +1 more source
Hepatobiliary ultrasound is the most common initial diagnostic modality in the early detection of biliary atresia. It is not the gold standard, but the hepatobiliary ultrasound examination can be used to determine the appropriate further management ...
Kristin Agustina +5 more
doaj +1 more source
Biliary Atresia: Clinical Phenotypes and Aetiological Heterogeneity
Biliary atresia (BA) is an obliterative condition of the biliary tract that presents with persistent jaundice and pale stools typically in the first few weeks of life. While this phenotypic signature may be broadly similar by the time of presentation, it
M. Davenport +2 more
semanticscholar +1 more source

