Search Results - "Chee, Y"
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Loop‐mediated isothermal amplification (LAMP): a versatile technique for detection of micro‐organisms
Published in Journal of applied microbiology (01-03-2018)“…Summary Loop‐mediated isothermal amplification (LAMP) amplifies DNA with high specificity, efficiency and rapidity under isothermal conditions by using a DNA…”
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The gastrointestinal microbiome, small bowel bacterial overgrowth, and microbiome modulators in cystic fibrosis
Published in Pediatric pulmonology (01-09-2024)“…People with cystic fibrosis (pwCF) have an altered gastrointestinal microbiome. These individuals also demonstrate propensity toward developing small…”
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Cystic fibrosis from the gastroenterologist's perspective
Published in Nature reviews. Gastroenterology & hepatology (01-03-2016)“…Key Points Cystic fibrosis is a life-limiting disease caused by different mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and…”
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Impact of Gene Modifiers on Cystic Fibrosis Phenotypic Profiles: A Systematic Review
Published in Human mutation (01-01-2024)“…Cystic fibrosis (CF) is a complex monogenic disorder with a large variability in disease severity. Growing evidence suggests that the variation observed…”
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The Enigmatic Gut in Cystic Fibrosis: Linking Inflammation, Dysbiosis, and the Increased Risk of Malignancy
Published in Current gastroenterology reports (01-02-2017)“…Purpose of Review Intestinal inflammation, dysbiosis, and increased gastrointestinal malignancy risks are well-described in patients with cystic fibrosis (CF)…”
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Gut Microbiota in Children With Cystic Fibrosis: A Taxonomic and Functional Dysbiosis
Published in Scientific reports (09-12-2019)“…Intestinal dysbiosis has been observed in children with cystic fibrosis (CF), yet the functional consequences are poorly understood. We investigated the…”
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Probiotics for people with cystic fibrosis
Published in Cochrane database of systematic reviews (22-01-2020)“…Cystic fibrosis (CF) is a multisystem disease and the importance of growth and nutrition has been well established, given its implications for lung function…”
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Impact of CFTR modulation with Ivacaftor on Gut Microbiota and Intestinal Inflammation
Published in Scientific reports (13-12-2018)“…Cystic fibrosis (CF) is caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Next to progressive airway disease, CF is…”
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Critical disease burdens of Australian adults with cystic fibrosis: Results from an online survey
Published in Pediatric pulmonology (01-07-2023)“…Background The objective of this study was to conduct a web‐based questionnaire to investigate self‐reported phenotypes and disease burdens of individuals…”
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Guidelines on the assessment of bleeding risk prior to surgery or invasive procedures British Committee for Standards in Haematology
Published in British journal of haematology (01-03-2008)“…Unselected coagulation testing is widely practiced in the process of assessing bleeding risk prior to surgery. This may delay surgery inappropriately and cause…”
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Impact of highly effective modulator therapy on gastrointestinal symptoms and features in people with cystic fibrosis
Published in Paediatric respiratory reviews (20-09-2024)“…•An analysis on the impact of highly effective modulator therapy on gastrointestinal symptoms and features in pwCF.•The benefits of…”
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Cystic Fibrosis-related Liver Disease is Associated With Increased Disease Burden and Endocrine Comorbidities
Published in Journal of pediatric gastroenterology and nutrition (01-06-2020)“…Cystic fibrosis-related liver disease (CFLD) is the leading nonpulmonary cause of mortality in cystic fibrosis (CF). We evaluated and compared the burden of…”
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Disrupted progression of the intestinal microbiota with age in children with cystic fibrosis
Published in Scientific reports (04-05-2016)“…Cystic fibrosis (CF) is a genetic disorder that leads to formation of thick epithelial secretions in affected organs. Chronic microbial infections associated…”
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Resuscitating Cardiopulmonary Resuscitation Training in a Virtual Reality: Prospective Interventional Study
Published in Journal of medical Internet research (29-07-2021)“…Background Simulation-based technologies are emerging to enhance medical education in the digital era. However, there is limited data for the use of virtual…”
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What Do We Know about the Microbiome in Cystic Fibrosis? Is There a Role for Probiotics and Prebiotics?
Published in Nutrients (22-01-2022)“…Cystic fibrosis (CF) is a life-shortening genetic disorder that affects the cystic fibrosis transmembrane conductance regulator (CFTR) protein. In the…”
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Pancreatitis and pancreatic cystosis in Cystic Fibrosis
Published in Journal of cystic fibrosis (01-11-2017)“…The pathologic effects of an altered cystic fibrosis transmembrane receptor (CFTR) protein on the exocrine pancreas is ubiquitous and of varying severity. In…”
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Body composition and body mass index measures from 8 to 18 years old in children with cystic fibrosis
Published in Journal of cystic fibrosis (01-09-2023)“…Historically, body mass index (BMI) >50th percentile has represented optimal nutritional status in children with cystic fibrosis (CF) due to its positive…”
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Role of upfront autologous transplant for peripheral T-cell lymphoma patients achieving a complete remission with first-line therapy: a systematic review and meta-analysis
Published in Bone marrow transplantation (Basingstoke) (01-06-2024)“…There is currently no consensus on the role of upfront autologous transplantation (ASCT) for patients with peripheral T-cell lymphomas (PTCL), especially in…”
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Cystic Fibrosis‐related Liver Disease is Associated With Increased Disease Burden and Endocrine Comorbidities
Published in Journal of pediatric gastroenterology and nutrition (01-06-2020)“…ABSTRACT Background: Cystic fibrosis‐related liver disease (CFLD) is the leading nonpulmonary cause of mortality in cystic fibrosis (CF). We evaluated and…”
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