[This corrects the article DOI: 10.1371/journal.pone.0228391.].
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147733 | PMC |
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0231911 | PLOS |
J Pediatr
December 2024
Division of Pediatric Emergency Medicine, Department of Pediatrics, Hospital for Sick Children and University of Toronto; Toronto, Canada. Electronic address:
Objectives: To examine pediatrician diagnostic skill development of dermatology image-based cases via a web-based tool and to determine case-level variables that were associated with diagnostic error.
Study Design: This was a multi-center, prospective, cross-sectional study. A convenience sample of pediatric trainees and attendings were eligible for participation.
Pediatr Radiol
December 2024
Department of Diagnostic Radiology, Division of Pediatric Radiology, Dalhousie University, IWK Health, 5850/5980 University Avenue, PO Box 9700, Halifax, NS, B3K 6R8, Canada.
Clin Trials
November 2024
Population Health Research Institute, Hamilton, ON, Canada.
Background: Over the course of a clinical trial, irregularities may arise in the data. Trialists implement human-intensive, expensive central statistical monitoring procedures to identify and correct these irregularities before the results of the trial are analyzed and disseminated. Machine learning algorithms have shown promise for identifying center-level irregularities in multi-center clinical trials with minimal human intervention.
View Article and Find Full Text PDFAesthetic Plast Surg
November 2024
Department of Plastic Surgery, Peking University Third Hospital, #49, North Garden Road, Haidian District, Beijing, People's Republic of China.
Background: The chin significantly influences facial aesthetics, contributing to the overall balance and harmony of the face. This study aimed to assess the effectiveness of the hyaluronic acid filler Hyamax® Volumizer for chin augmentation and correction of chin retrusion compared to a no-treatment control.
Methods: Participants aged 18-55 years with mild to moderate chin retrusion were randomized in a 3:1 ratio to receive either the treatment group (n = 150) or control group (n = 50).
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