Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Mark R. Oliver"'
Publikováno v:
JGH Open, Vol 6, Iss 12, Pp 818-823 (2022)
Abstract Despite evidence of an increased prevalence of irritable bowel syndrome (IBS) in adults with inflammatory bowel disease (IBD) compared with the general population, the prevalence of IBS in children with IBD is unclear. In this review, we aim
Externí odkaz:
https://doaj.org/article/fd8d59d7e83040bb9280eff4e1d9f905
Autor:
Helen M. Evans, Elena Kondratyeva, Mark R. Oliver, Carla Colombo, Isabelle de Monestrol, F. Alghisi, Rita Padoan, Chee Y. Ooi, Grant A. Ramm, Nataliya Kashirskaya, Fabiola Corti, Gianfranco Alicandro, Peter Lewindon, Anders Lindblad, I. Asherova, Birgitta Strandvik
Publikováno v:
Journal of Cystic Fibrosis. 21:220-226
Background The efficacy and safety of ursodeoxycholic acid (UDCA) for the treatment of liver disease associated with cystic fibrosis (CF) are under discussion, and clinical practice varies among centers. The study aimed at evaluating if the incidence
Autor:
Carlos E. Prada, Mark R. Oliver, Jessica Wen, Joy Lee, Heidi Peters, Winita Hardikar, Hernan Eiroa, Sarah Donoghue, Amit A. Shah, Kathleen M. Loomes, Kathryn Clarkston, Akihiro Asai
Publikováno v:
Am J Med Genet A
We describe 10 females with ornithine transcarbamylase (OTC) deficiency and liver dysfunction, revealing a unique pattern of hepatocyte injury in which initial hyperammonemia and coagulopathy is followed by a delayed peak in aminotransferase levels.
Autor:
Susan M. White, Mark R. Oliver, Theresa Cole, David S. Francis, Lauren S. Akesson, Peter J Simm, Michelle G. de Silva
Publikováno v:
Journal of Paediatrics and Child Health. 57:1109-1112
Publikováno v:
JGH open : an open access journal of gastroenterology and hepatology. 6(12)
Despite evidence of an increased prevalence of irritable bowel syndrome (IBS) in adults with inflammatory bowel disease (IBD) compared with the general population, the prevalence of IBS in children with IBD is unclear. In this review, we aimed to ide
Publikováno v:
Canadian Journal of Gastroenterology, Vol 9, Iss 5, Pp 281-284 (1995)
A six-year-old boy with Ménétriér's disease, which developed in association with an intercurrent cytomegalovirus (CMV) infection, is presented. This case illustrates the clinical features, natural history and self-limited nature of this rare cause
Externí odkaz:
https://doaj.org/article/9428b9eead4c419fb9558e9ac411700b
Publikováno v:
Canadian Journal of Gastroenterology, Vol 9, Iss 4, Pp 217-220 (1995)
An infant girl who presented with cholestasis and hepatitis that rapidly progressed to fulminant liver failure is reported. Postmortem examination yielded a diagnosis of demonstrated extensive hepatic necrosis due to adenovirus type 5 infection which
Externí odkaz:
https://doaj.org/article/f7d8c691579048dba75535276798f8ed
Autor:
John Widger, Mark R Oliver, Michele O'Connell, Fergus J Cameron, Sarath Ranganathan, Phil J Robinson
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e44844 (2012)
BACKGROUND: Patients with Cystic Fibrosis (CF) are relatively insulinopenic and are at risk of diabetes, especially during times of stress. There is a paucity of data in the literature describing glucose tolerance during CF pulmonary exacerbations. W
Externí odkaz:
https://doaj.org/article/250827a930514ba998a28b186a3c15cd
Autor:
Mark R Oliver, R Brent Scott, Robin C Eccles, Cynthia Trevenen, Jonathon B Meddings, Steven R Martin
Publikováno v:
Canadian Journal of Gastroenterology, Vol 8, Iss 4, Pp 253-256 (1994)
This case report of a six-year-old child with Peutz-Jeghers syndrome illustrates the potential diversity of presenting gastrointestinal symptoms and signs including hematemesis, obstruction and recurrent intussusception. Endoscopy was useful in asses
Externí odkaz:
https://doaj.org/article/ed102c594da1472b8209752ebaaa4d3e
Autor:
Chee Y. Ooi, Kristyn Ford, Peter Lewindon, Natalie van der Haak, Rishi Bolia, Jo Harrison, Jonathan Bishop, Mark R. Oliver, Sarath Ranganathan
Publikováno v:
Journal of Paediatrics and Child Health. 54:609-619
Cystic fibrosis (CF) is the most common, life-shortening, genetic illness affecting children in Australia and New Zealand. The genetic abnormality results in abnormal anion transport across the apical membrane of epithelial cells in a number of organ