Publications by authors named "G W Stamp"

Pain is an interpersonal and inherently social experience. Pain perception and administration of medical treatment all occur in a particular environmental and social context. Early environmental influences and early learning experiences and interactions condition the body's response to different threats (like pain), ultimately shaping the underlying neurophysiology.

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Article Synopsis
  • Mucosal (MM) and acral melanomas (AM) are rare types of melanoma that often have KIT mutations, which could be treated with targeted small-molecule inhibitors, though none are currently approved for melanoma.
  • A Phase II clinical trial (NICAM) assessed the safety and effectiveness of nilotinib in patients with KIT-mutant MM and AM; 18% of screened patients had KIT mutations, with some showing promising results.
  • The trial found that nilotinib demonstrated activity in treating these mutations, suggesting the need for further research on its use in managing KIT-mutated melanoma.
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Purpose: We conducted a retrospective analysis of prospectively collected data to evaluate (1) the extent of surgical correction following minimally invasive periacetabular osteotomy, (2) improvements in functional outcomes and any potential predictors for favourable outcome, and (3) complications after minimally invasive periacetabular osteotomy.

Methods: A total of 352 minimally invasive periacetabular osteotomy procedures were performed on 312 hip dysplasia patients between 2013 and 2020. Radiological parameters such as lateral centre edge angle, acetabular index, and Tönnis grade of arthritis were calculated.

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Unlabelled: Understanding the evolutionary pathways to metastasis and resistance to immune-checkpoint inhibitors (ICI) in melanoma is critical for improving outcomes. Here, we present the most comprehensive intrapatient metastatic melanoma dataset assembled to date as part of the Posthumous Evaluation of Advanced Cancer Environment (PEACE) research autopsy program, including 222 exome sequencing, 493 panel-sequenced, 161 RNA sequencing, and 22 single-cell whole-genome sequencing samples from 14 ICI-treated patients. We observed frequent whole-genome doubling and widespread loss of heterozygosity, often involving antigen-presentation machinery.

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