Results 11 to 20 of about 11,497 (209)

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, Benedikt Kaufmann, Maria Eugenia Inzaugarat, Theresa Maria Holtmann, Lukas Geisler, Jana Hundertmark, Marlene Sophia Kohlhepp, Laela M. Boosheri, Daisy R. Chilin‐Fuentes, Amanda Birmingham, Kathleen M. Fisch, Joel D. Schilling, Sven H. Loosen, Christian Trautwein, Christoph Roderburg, Münevver Demir, Frank Tacke, Hal M. Hoffman, Ariel E. Feldstein, Alexander Wree   +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, Kieran Hawthorne, Kenneth D. R. Setchell, Monica Narvaez Rivas, Lisa Henn, Charlotte A. Beil, Saul J. Karpen, Vicky L. Ng, Estella M. Alonso, Jorge A. Bezerra, Stephen L. Guthery, Simon Horslen, Kathy M. Loomes, Patrick McKiernan, John C. Magee, Robert M. Merion, Jean P. Molleston, Philip Rosenthal, Richard J. Thompson, Kasper S. Wang, Ronald J. Sokol, Benjamin L. Shneider, for Childhood Liver Disease Research Network (ChiLDReN)   +22 more
wiley   +1 more source

Waitlist mortality of young patients with biliary atresia: Impact of allocation policy and living donor liver transplantation

Liver Transplantation, EarlyView., 2022
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, Marieke van Rosmalen, Patrick F. van Rheenen, Marieke T. de Boer, Aad P. van den Berg, Hubert P. J. van der Doef, Michel Rayar, Ruben H.J. de Kleine, Robert J. Porte, Vincent E. de Meijer, Henkjan J. Verkade   +10 more
wiley   +1 more source

Intestinal Atresia

Clinics in Perinatology, 1978
Forty-five patients with intestinal atresia, including 20 with duodenal, 21 with jejunoileal, and 3 with colonic obstruction, were encountered at the Yale-New Haven Hospital between 1970 and 1976. The overall survival rate in the 43 operated cases was 93 per cent.
J A, Olvera Durán, R, Peniche García
openaire   +4 more sources

Staged surgical treatment of apple peel intestinal atresia

Journal of Pediatric Surgery Case Reports, 2019
Apple peel atresia is an uncommon cause of intestinal obstruction. The authors report a case of a 36 weeks preterm girl, presenting with a fetal intestinal obstruction on prenatal ultrasonography, that was intraoperatively diagnosed with small bowel ...
Jalles Filipa, Morgado Mariana, Janeiro Marta, Gonçalves Miroslava   +3 more
doaj   +1 more source

Use of feeding jejunostomy in a type IV jejuno-ileal atresia in a low-income country

Journal of Pediatric Surgery Case Reports, 2020
Intestinal atresia is a rarely reported congenital anomaly in Haiti. To date there exists little to no published data describing the management of this entity in Haiti.
Patrick Charlorin, Osnel Louima, Gabriel Steve Pierre, Roberto Peigne, Alexis Bowder, Andriani Grazia Maria, Augustin Sylvio   +6 more
doaj   +1 more source

Jejunal atresia due to heterotopic pancreatic intussusception

Journal of Pediatric Surgery Case Reports, 2021
Jejunal atresia is a common cause of neonatal intestinal obstruction that requires surgical correction and may be caused by intestinal volvulus, intussusception, or internal hernia. A 1-day-old female infant was referred to our hospital for evaluation of
So-Hyun Nam, Song-Hee Han
doaj   +1 more source

Fenestrated Colonic Atresia: A rare presentation

Journal of Pediatric Surgery Case Reports, 2020
Congenital Colonic Atresia is described to be the rarest form of intestinal atresia and many anomalies can be associated with it. Surgical repair is the definitive treatment but managing it with primary anastomosis vs intestinal diversion is still being ...
Mohamad H. El Mahmoud, Shehanah F. Al Omair, Tahani N. Alrashidi   +2 more
doaj   +1 more source

Duodeno-jejunal Atresia with Apple-peel Appearance of the Remaining Ileum: A Rare Association

MAMC Journal of Medical Sciences, 2015
Intestinal atresia is a common cause of neonatal intestinal obstruction. We present a rare case of duodenal atresia, multiple jejunal atresias, and apple peel appearance of the remaining ileum in a 3-day-old neonate.
Abhishek Chinya, Simmi K Ratan, Satish Kumar Aggarwal   +2 more
doaj   +1 more source

Acquired Jejunal Atresia in a 2-Month-old Infant [PDF]

Journal of Clinical and Diagnostic Research, 2015
Acquired intestinal atresia in non–necrotizing enterocolitis affected patients is very rare. We report a 2 month old male infant who presented with bilious vomiting, abdominal distension and constipation. He was exclusively breast fed, gained weight and
Ankur Mandelia, Sandeep Agarwala
doaj   +1 more source