Zobrazeno 1 - 10
of 198
pro vyhledávání: '"Chee Y Ooi"'
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:
Michael J Coffey, Ivan Low, Sacha Stelzer-Braid, Bernd Wemheuer, Millie Garg, Torsten Thomas, Adam Jaffe, William D Rawlinson, Chee Y Ooi
Publikováno v:
PLoS ONE, Vol 15, Iss 5, p e0233557 (2020)
Intestinal bacterial dysbiosis is evident in children with cystic fibrosis (CF) and intestinal viruses may be contributory, given their influence on bacterial species diversity and biochemical cycles. We performed a prospective, case-control study on
Externí odkaz:
https://doaj.org/article/1b4788400dab4b23be75642ad0d102a2
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:
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:
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
Autor:
Aliye, Uc, Gretchen A, Cress, Fuchenchu, Wang, Maisam, Abu-El-Haija, Kate M, Ellery, Douglas S, Fishman, Cheryl E, Gariepy, Tanja, Gonska, Tom K, Lin, Quin Y, Liu, Megha, Mehta, Asim, Maqbool, Brian A, McFerron, Veronique D, Morinville, Chee Y, Ooi, Emily R, Perito, Sarah Jane, Schwarzenberg, Zachary M, Sellers, Jose, Serrano, Uzma, Shah, David M, Troendle, Michael, Wilschanski, Yuhua, Zheng, Ying, Yuan, Mark E, Lowe
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 75(5)
The objective of this study is to investigate risk factors and disease burden in pediatric acute recurrent pancreatitis (ARP) and chronic pancreatitis (CP).Data were obtained from INternational Study group of Pediatric Pancreatitis: In search for a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c26e046ebb5c94d5d4941f4fedd9b30a
https://pubmed.ncbi.nlm.nih.gov/35976273
https://pubmed.ncbi.nlm.nih.gov/35976273
Publikováno v:
Nutrients, Vol 14, Iss 3, p 480 (2022)
Cystic fibrosis (CF) is a life-shortening genetic disorder that affects the cystic fibrosis transmembrane conductance regulator (CFTR) protein. In the gastrointestinal (GI) tract, CFTR dysfunction results in low intestinal pH, thick and inspissated m
Externí odkaz:
https://doaj.org/article/82f8da6031574f99ba55fb3089321d99
Autor:
Carla Colombo, Grant A Ramm, Anders Lindblad, Fabiola Corti, Luigi Porcaro, Federico Alghisi, Irina Asherova, Helen Evans, Nataliya Kashirskaya, Elena Kondratyeva, Peter J Lewindon, Isabelle de Monestrol, Mark Oliver, Chee Y. Ooi, Rita Padoan, Sahana Shankar, Gianfranco Alicandro
Publikováno v:
Journal of Cystic Fibrosis. 22:263-265
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e1932592aa4ab45a6b1a060c1fea7f3
https://doi.org/10.1016/j.jcf.2023.01.012
https://doi.org/10.1016/j.jcf.2023.01.012