Publications by authors named "K W Conway"

The mesenchymal transformations of infiltrating gliomas are uncommon events. This is particularly true of IDH-mutant astrocytomas and oligodendrogliomas, in which mesenchymal transformation is exceedingly rare. oligosarcoma is a newly recognized methylation class (MC) that represents transformed 1p/19q co-deleted oligodendrogliomas, but recent studies indicate it may be non-specific.

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Objective: The authors compared the performance of a novel self-collect device with clinician-collected samples for detection of high-risk human papillomavirus (hrHPV).

Materials And Methods: Eighty-two (82) participants were recruited from 5 clinical sites in the United States. Each participant performed self-collect sampling using the self-collect device followed by a standard of care clinician-collected sample.

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This case report describes a remarkable improvement in bone mineral density (BMD) in a 95-year-old female with parathyroid hormone (PTH)-mediated hypercalcemia following treatment with zoledronic acid. Despite her complex medical history, including chronic kidney disease (CKD) and osteoporosis, the patient experienced a significant increase in bone density, particularly in the left femoral neck, while maintaining stable renal function. This case highlights the efficacy and safety of zoledronic acid in elderly patients with osteoporosis and hypercalcemia, emphasizing the importance of careful monitoring to prevent renal complications.

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Article Synopsis
  • A study using data from the MD STARnet examined respiratory testing and insufficiency in people with facioscapulohumeral muscular dystrophy (FSHD) diagnosed between 2008-2016.
  • Out of 170 individuals with FSHD, only 20% received pulmonary function tests, and 14.1% had polysomnograms; however, over half of those tested showed significant respiratory issues.
  • The findings suggest a need for better monitoring and adherence to guidelines recommending that all FSHD patients receive baseline respiratory evaluations to identify complications early.
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Article Synopsis
  • The study investigates the prevalence of omphalocele, a serious congenital defect, in a large cohort of live births in Denmark from 1997-2021.
  • More than half of the infants with omphalocele were found to have additional major malformations, indicating a significant risk for complications.
  • These findings emphasize the need to consider the long-term healthcare requirements for infants with omphalocele and associated syndromes.
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