Results 21 to 30 of about 21,958 (289)
Biology and postnatal development of organ systems of cynomolgus monkeys (Macaca fascicularis)
Journal of Medical Primatology, Volume 52, Issue 1, Page 64-78, February 2023., 2023 Abstract Background The cynomolgus macaque has become the most used non‐human primate species in nonclinical safety assessment during the past decades. Methods This review summarizes the biological data and organ system development milestones of the cynomolgus macaque available in the literature.
Xiantang Li +5 more
wiley +1 more source
The Association Between Biliary Atresia and Cytomegalovirus Infection [PDF]
, 2017 Perinatal infection of cytomegalovirus (CMV) may cause cholestasis resembling biliary atresia. CMV infection is found in patients with biliary atresia. This simultaneous occurrence of biliary atresia and CMV infection prompted
Kumaheri, M. A. (Meutia) +1 more
core +2 more sources
Development of extrahepatic bile ducts and mechanisms of tumorigenesis: Lessons from mouse models
Pathology International, Volume 72, Issue 12, Page 589-605, December 2022., 2022 Abstract The biliary system is a highly branched tubular network consisting of intrahepatic bile ducts (IHBDs) and extrahepatic bile ducts (EHBDs). IHBDs are derived from hepatic progenitor cells, while EHBDs originate directly from the endoderm through a separate branching morphogenetic process.
Hiroyuki Tomita, Akira Hara
wiley +1 more source
Biliary Atresia Associated with Jejunal Atresia and a Review of the Literature in Japan
Asian Journal of Surgery, 2005 An unusual case of biliary atresia with jejunal atresia is herein described. Only 12 cases demonstrating biliary atresia associated with a jejunal atresia have been previously reported in Japan.
Koushi Asabe +4 more
doaj +1 more source
BMC Pediatrics, 2020 Background Early distinguishing biliary atresia from other causes of infantile cholestasis remains a major challenge. We aimed to develop and validate a scoring system based on bile acid for identification of biliary atresia.
Dongying Zhao +4 more
doaj +1 more source
The Successful Administration of Steroid in Extrahepatic Cholestasis
Journal of Community Medicine and Public Health Research, 2023 Biliary atresia is the most common cause of liver transplantation in children. Kasai surgery is still a bridging therapy for biliary atresia, but patients are often late for treatment.
Anindya Kusuma Winahyu +3 more
doaj +1 more source
Live transplantation in children with biliary atresia and vascular anomalies [PDF]
, 1974 Eight of 29 infants and children undergoing orthotopic liver transplantation for extrahepatic biliary atresia had associated major vascular anomalies.
Lilly, JR, Starzl, TE
core +1 more source
Journal of Indian Association of Pediatric Surgeons, 2008 Biliary atresia (BA) is a cholangiodestructive disease affecting biliary tract, which ultimately leads to cirrhosis, liver failure and death if not treated. The incidence is higher in Asian countries than in Europe. Up to 10% of cases have other congenital anomalies, such as polysplenia, asplenia, situs inversus, absence of inferior vena cava and pre ...
Sinha, C.K., Davenport, Mark
openaire +3 more sources
Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome [PDF]
, 2018 Published histologic studies of the hilar plate or entire biliary remnant at the time of Kasai portoenterostomy (KHPE) have not provided deep insight into the pathogenesis of biliary atresia, relation to age at surgery, prognosis or the basis for ...
Arva +32 more
core +1 more source
JHEP Reports, 2023 Background & Aims: Progressive familial intrahepatic cholestasis type 3 (PFIC3) is a rare liver disease caused by biallelic variations in ABCB4. Data reporting on the impact of genotype and of response to ursodeoxycholic acid (UDCA) therapy on long ...
Emmanuel Gonzales +18 more
doaj