Results 11 to 20 of about 402,747 (185)

Evaluation of intestinal damage biomarkers in calves with atresia coli

Journal of Veterinary Research, 2018
Intestinal obstruction such as atresia coli causes pathophysiological changes in gastrointestinal tissue due to the rise of intra-abdominal pressure. The aim of this study is to determine the intestinal damage with intestinal biomarkers in calves with ...
Yildiz Ramazan, Ok Mahmut, Ider Merve, Aydogdu Ugur, Naseri Amir, Parlak Kurtulus, Gulersoy Erdem   +6 more
doaj   +3 more sources

Jejunum ileal intestinal atresia. [PDF]

Medisur, 2005
The intestinal atresia is one of the most important causes of intestinal obstruction in newborn. They constitute aorund 95% of total intestinal obstructions in this age group. Most of intestinal atresias are jejunoieal atresia.
Claudio J. Puente Fonseca
doaj   +3 more sources

Atresia intestinal: a propósito de un caso [PDF]

Revista Peruana de Investigación Materno Perinatal, 2018
El tracto intestinal fetal puede ser alterado por numerosos procesos patológicos, los hallazgos ecográficos típicos de la obstrucción intestinal son dilatación de las asas intestinales en el abdomen fetal proximal a la obstrucción.
admin admin, Jaime Ingar-Pinedo, Erasmo Huertas-Tacchino, Oscar Antonio Limay-Ríos, Walter Castillo-Urquiaga, Mario Zarate-Girao, Lenin W Pérez-Arias, Luis M Diaz-Infantes   +7 more
doaj   +2 more sources

Apple-peel atresia presenting as foetal intestinal obstruction

African Journal of Paediatric Surgery, 2011
Apple-peel atresia or Type 3 jejuno-ileal atresia (JIA) is an uncommon cause of foetal intestinal obstruction. Bowel obstruction in the foetus is diagnosed on the prenatal ultrasonography only in 50% cases.
Ashok Yadavrao Kshirsagar, Sushma Rajaram Desai, Mayur Anant Nagvekar, Gaurav Om Prakash Vasisth   +3 more
doaj   +3 more sources

Concordant Intestinal Atresia in Two Pairs of Monozygotic Twins [PDF]

American Journal of Perinatology Reports, 2011
Intestinal atresia in both twins from the same pregnancy is very rare. Only seven pairs of twins have been described. The authors report on two cases of monozygotic twins with different types of intestinal atresia and clinical evolution.
Mario Giuffrè, Mariavalentina Catania, Giovanni Corsello   +2 more
doaj   +2 more sources

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

Congenital short bowel syndrome: Clinical aspects by systematic review. [PDF]

JPGN Rep
Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Remund B, Schibli S, Sokollik C.
europepmc   +2 more sources

Changes of smooth muscle contractile filaments in small bowel atresia [PDF]

, 2012
AIM: To investigate morphological changes of intestinal smooth muscle contractile fibres in small bowel atresia patients. METHODS: Resected small bowel specimens from small bowel atresia patients (n = 12) were divided into three sections (proximal ...
Rolle, Udo, Metzger, Roman, Fiegel, Henning C., Gfrörer, Stefan, Ramachandran, Priya   +4 more
core   +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