Results 181 to 190 of about 482,159 (313)
Reinforcement learning based automated anesthesia system for gastrointestinal endoscopy with a multicenter randomized trial. [PDF]
Bing HL +18 more
europepmc +1 more source
Abstract Lynch syndrome (LS) is the most common hereditary colorectal cancer syndrome, caused by a germline pathogenic variant in one of the mismatch repair (MMR) genes. Among these, MSH6‐associated LS represents a distinct subtype with unique molecular and clinical characteristics.
Salwa Ben Yahia +4 more
wiley +1 more source
Evaluating StyleGAN2-ADA and f-AnoGAN for GAN based unsupervised anomaly detection in gastrointestinal endoscopy. [PDF]
Bairwa AK +3 more
europepmc +1 more source
ABSTRACT Lynch syndrome (LS) is the most common hereditary colorectal cancer (CRC) syndrome and is characterized by an accelerated adenoma‐carcinoma sequence, a relatively higher prevalence of flat and subtle CRC precursor lesions, and exceptionally high adenoma miss rates despite intensive colonoscopy surveillance.
Robert Hüneburg +3 more
wiley +1 more source
Effect of Propofol Combined with Oliceridine versus Fentanyl on Desaturation During Gastrointestinal Endoscopy: A Randomized Clinical Trial. [PDF]
Xu F +14 more
europepmc +1 more source
Colorectal cancer screening reduces disease burden, but the comparative performance of screening strategies remains unclear. This population‐based study shows that the tandem strategy (positive results from both questionnaire‐based risk assessment and fecal immunochemical testing) substantially improved the detection rates of colorectal cancer and ...
Ruyue Liu +5 more
wiley +1 more source
Endoscopic clip systems for hemostasis and defect closure in gastrointestinal endoscopy. [PDF]
Aguila EJT, Lau LHS, Li JW, Berzin TM.
europepmc +1 more source
ABSTRACT Colorectal cancer (CRC) remains a leading cause of cancer‐related morbidity and mortality worldwide yet is largely preventable through effective screening and surveillance. While most CRC cases are sporadic, a substantial proportion occur in individuals at increased risk due to hereditary cancer syndromes or family history who require tailored
Ophir Gilad +5 more
wiley +1 more source

