Results 31 to 40 of about 111,824 (315)
BILIARY ATRESIA: Clinical and Research Challenges for the 21st Century
Hepatology, 2018 Biliary atresia (BA) is a fibroinflammatory disease of the intrahepatic and extrahepatic biliary tree. Surgical hepatic portoenterostomy (HPE) may restore bile drainage, but progression of the intrahepatic disease results in complications of portal ...
J. Bezerra +6 more
semanticscholar +1 more source
Interleukin‐18 signaling promotes activation of hepatic stellate cells in mouse liver fibrosis
Hepatology, EarlyView., 2022 Interleukin‐18 signaling promotes activation of hepatic stellate cells in mouse liver fibrosis. Abstract Background and Aims Nucleotide‐binding oligomerization domain‐like receptor‐family pyrin domain‐containing 3 (NLRP3) inflammasome activation has been shown to result in liver fibrosis.
Jana Knorr +19 more
wiley +1 more source
Serum bile acids as a prognostic biomarker in biliary atresia following Kasai portoenterostomy
Hepatology, EarlyView., 2022 Serum bile acid levels predict outcomes in patients with biliary atresia who achieve normalized bilirubin levels after Kasai portoenterostomy. Abstract Background and Aims In biliary atresia, serum bilirubin is commonly used to predict outcomes after Kasai portoenterostomy (KP).
Sanjiv Harpavat +22 more
wiley +1 more source
Reproductive strategies in black scabbardfish (Aphanopus carbo Lowe, 1839) from the NE Atlantic
Scientia Marina, 2009 Gonads of the NE Atlantic black scabbardfish were examined to give an insight into the reproductive biology of this species. It was concluded that black scabbardfish had determinate fecundity because: (i) a distinct hiatus in oocyte size was observed ...
Ana Neves +5 more
doaj +1 more source
Impacts of Early Kasai Portoenterostomy on Short‐Term and Long‐Term Outcomes of Biliary Atresia
Hepatology Communications, 2021 There are discrepancies regarding the clinical impact of age at Kasai portoenterostomy (KP) on surgical outcomes. Hence, we re‐assessed the clinical significance of age at KP.
Ryuji Okubo +3 more
doaj +1 more source
Orphanet Journal of Rare Diseases, 2001 Oesophageal atresia (OA) encompasses a group of congenital anomalies comprising of an interruption of the continuity of the oesophagus with or without a persistent communication with the trachea. In 86% of cases there is a distal tracheooesophageal fistula, in 7% there is no fistulous connection, while in 4% there is a tracheooesophageal fistula ...
openaire +3 more sources
Atretic ovarian follicles morphology and immunolocalization of active caspase-3 in algerian bedouin goat (capra hircus) ovaries [PDF]
Kafkas Universitesi Veteriner Fakültesi Dergisi, 2018 This study aims to highlight the cellular and molecular events of atresia in the Bedouin goat ovarian follicles. Ovaries collected from slaughterhouses during breeding and non-breeding seasons were submitted to morphological studies and ...
Sara KASSOURI-MAOUCHE +7 more
doaj +1 more source
Liver transplantation, 2017 Biliary atresia (BA) is a progressive, fibro‐obliterative disorder of the intrahepatic and extrahepatic bile ducts in infancy. The majority of affected children will eventually develop end‐stage liver disease and require liver transplantation (LT ...
Shikha S. Sundaram +3 more
semanticscholar +1 more source
Nature Reviews Disease Primers, 2019 This PrimeView highlights oesophageal atresia, a congenital abnormality of the oesophagus that requires surgical reconstruction soon after birth.
M. van Lennep +8 more
semanticscholar +2 more sources
The journal of international advanced otology, 2019 The aim of this report is to provide international recommendations for functional ear reconstruction in patients with microtia and aural atresia.
Tian-Yu Zhang +8 more
semanticscholar +1 more source