Zobrazeno 1 - 10
of 1 497
pro vyhledávání: '"Chee Y"'
Autor:
Su Min Joyce Tan, Michael J. Coffey, Katrina Blazek, Neela Sitaram, Isabella Dobrescu, Alberto Motta, Sandra Chuang, Chee Y. Ooi
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Background and aimThe COVID-19 pandemic necessitated the transition to online medical education. This study evaluated the efficacy of online case-based tutorials using a serious game tutorial [PlayMed™ (PM)], as compared to a traditional slideshow
Externí odkaz:
https://doaj.org/article/9317235a715d457b84e66aac08d905d6
Autor:
Nisha E. Mathew, Delyse McCaffrey, Adam K. Walker, Kylie-Ann Mallitt, Anne Masi, Margaret J. Morris, Chee Y. Ooi
Publikováno v:
Molecular Autism, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract Background Gastrointestinal symptoms and inflammatory gastrointestinal diseases exist at higher rates in the autistic population. It is not clear however whether autism is associated with elevated gastrointestinal inflammation as studies exa
Externí odkaz:
https://doaj.org/article/73152531d9f34713853946ee2224e06d
Autor:
Tamarah E. Katz, Claire E. Wakefield, Christina Signorelli, Andrew S. Day, Angharad Vernon-Roberts, Chee Y. Ooi
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionGastrointestinal (GI) symptoms are common in individuals with Cystic Fibrosis (CF). International research has highlighted that GI care for this group of patients is lacking. Gastroenterology services to CF clinics across Australasia are
Externí odkaz:
https://doaj.org/article/50a3c40358b14449bc23eeb775f9395d
Autor:
Isabelle McKay, Josie van Dorst, Tamarah Katz, Michael Doumit, Bernadette Prentice, Louisa Owens, Yvonne Belessis, Sandra Chuang, Adam Jaffe, Torsten Thomas, Michael Coffey, Chee Y. Ooi
Publikováno v:
Gut Microbes, Vol 15, Iss 1 (2023)
ABSTRACTCystic fibrosis (CF) is a multisystem, autosomal, recessive disease primarily affecting the lungs, pancreas, gastrointestinal tract, and liver. Whilst there is increasing evidence of a microbial ‘gut-lung axis’ in chronic respiratory cond
Externí odkaz:
https://doaj.org/article/0405a8d452fa422eb472bfd16dd90ace
Publikováno v:
Medicine in Microecology, Vol 13, Iss , Pp 100057- (2022)
Cystic fibrosis (CF) is a multisystem genetic disease which affects numerous organs in the body. Patients with CF exhibit profound alterations in the gastrointestinal microbiome, characterised by an increase in pathogenic bacteria and reduction in be
Externí odkaz:
https://doaj.org/article/d53ee5eb4158482d8320cebdf2208c13
Autor:
Isabelle R. McKay, Chee Y. Ooi
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Cystic fibrosis (CF) is a common disorder of autosomal recessive inheritance, that once conferred a life expectancy of only a few months. Over recent years, significant advances have been made to CF therapeutic approaches, changing the face of the di
Externí odkaz:
https://doaj.org/article/0f405b1c68784a92a5bf1b2fac0e676a
Autor:
Sharon L. Wong, Nikhil T. Awatade, Miro A. Astore, Katelin M. Allan, Michael J. Carnell, Iveta Slapetova, Po-chia Chen, Alexander Capraro, Laura K. Fawcett, Renee M. Whan, Renate Griffith, Chee Y. Ooi, Serdar Kuyucak, Adam Jaffe, Shafagh A. Waters
Publikováno v:
iScience, Vol 25, Iss 1, Pp 103710- (2022)
Summary: Characterization of I37R, a mutation located in the lasso motif of the CFTR chloride channel, was conducted by theratyping several CFTR modulators from both potentiator and corrector classes. Intestinal current measurements in rectal biopsie
Externí odkaz:
https://doaj.org/article/9a4dc92c469442f8afda25d75b18cedf
Autor:
Janaya Elizabeth Perron, Michael Jonathon Coffey, Andrew Lovell-Simons, Luis Dominguez, Mark E King, Chee Y Ooi
Publikováno v:
Journal of Medical Internet Research, Vol 23, Iss 7, p e22920 (2021)
BackgroundSimulation-based technologies are emerging to enhance medical education in the digital era. However, there is limited data for the use of virtual reality simulation in pediatric medical education. We developed Virtual Doc as a highly immers
Externí odkaz:
https://doaj.org/article/953ef437ff6a4fdb9d2b2ccdf6c232ae
Autor:
Chee Y. Ooi, Rosie Sutherland, Carlo Castellani, Katherine Keenan, Margaret Boland, Joe Reisman, Candice Bjornson, Mark A. Chilvers, Richard van Wylick, Steven Kent, April Price, Dimas Mateos-Corral, Daniel Hughes, Melinda Solomon, Peter Zuberbuhler, Janna Brusky, Peter R. Durie, Felix Ratjen, Tanja Gonska
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-7 (2019)
Abstract Background Newborn screening (NBS) for cystic fibrosis (CF) not only identifies infants with a diagnosis of CF, but also those with an uncertain diagnosis of cystic fibrosis (CF), i.e. CF transmembrane conductance regulator (CFTR)-related me
Externí odkaz:
https://doaj.org/article/7b7dc0389d05407d9f20efd82bd3212f
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-4 (2019)
Abstract Background Cholecystoduodenostomy is a surgical procedure that bypasses the extrahepatic biliary tree and connects the gallbladder directly to the duodenum. This case describes the successful use of this procedure in a novel situation. Case
Externí odkaz:
https://doaj.org/article/7b399fc1a7224c9691e4e9e34514e9be