Publications by authors named "V C Wright"

Mycoplasma pneumoniae causes atypical pneumonia in children and young adults. Its lack of a cell wall makes it resistant to beta-lactams, which are the first-line treatment for typical pneumonia. Current diagnostic tests are time-consuming and have low specificity, leading clinicians to administer empirical antibiotics.

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Older age is often conceptualised as a stage of life in which the future is considered to be less relevant than the past. This is reflected in literature that emphasises the importance of the past in later life but overlooks the significance of the future. This paper addresses this knowledge gap by analysing narratives that older people write about the future.

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Multisystem inflammatory syndrome in children (MIS-C) is a rare condition following SARS-CoV-2 infection associated with intestinal manifestations. Genetic predisposition, including inborn errors of the OAS-RNAseL pathway, has been reported. We sequenced 154 MIS-C patients and utilized a novel statistical framework of gene burden analysis, "burdenMC," which identified an enrichment for rare predicted-deleterious variants in BTNL8 (OR = 4.

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Objective: To assess 30-day outcomes of da Vinci robotic-assisted (dV-RAS) versus laparoscopic/thoracoscopic (lap/VATS) or open oncologic surgery.

Summary Background Data: Complex procedures in deep/narrow spaces especially benefit from dV-RAS. Prior procedure-specific comparisons are not generalizable.

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Article Synopsis
  • Diagnosing pediatric tuberculosis (TB) is complicated, but changes in host gene expression in blood can help identify biomarkers and improve understanding of the immune response in children with TB.* -
  • The study involved stimulating blood samples from 102 children with confirmed TB, TB infection, pneumonia, and healthy controls, and analyzing the gene expression differences using microarrays.* -
  • Researchers identified specific gene signatures that effectively distinguish TB from pneumonia, with high accuracy (AUC of 100% for one gene and 91.7% for a combination of two genes), paving the way for new diagnostic tests aligned with WHO standards.*
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