Jacqueline Kurz

Dr. Jacqueline Kurz

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Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 September 2019 in Pathogens
Verified
Journal Article
Open access
PDF file
JWJonna B. Westover
Jonna B. Westover
BHBrady Hickerson
Brady Hickerson
Arnaud Van WettereArnaud Van Wettere
Arnaud Van Wettere
BHBrett L. Hurst
Brett L. Hurst
JKJacqueline Kurz
Jacqueline Kurz
BGBrian Gowen
Brian Gowen
Severe fever with thrombocytopenia syndrome (SFTS) is an emerging viral hemorrhagic fever (VHF) endemic to China, South Korea, Japan, and Vietnam. Here we characterize the pathogenesis and natural history of disease in IFNAR-/- mice challenged with the HB29 strain of SFTS virus (SFTSV) and demonstrate hallmark features of VHF such as vascular leak and high concentrations of proinflammatory cytokines in blood and tissues. Treatment with FX06, a natural plasmin digest product of fibrin in clinical development as a treatment for vascular leak, reduced vascular permeability associated with SFTSV infection but did not significantly improve survival outcome. Further studies are needed to assess the role of vascular compromise in the SFTS disease process modeled in IFNAR-/- mice.

5 April 2018 in Veterinary Sciences
Verified
Journal Article
Open access
PDF file
JKJacqueline Kurz
Jacqueline Kurz
KSKate Schoenhals
Kate Schoenhals
GHGordon A. Hullinger
Gordon A. Hullinger
Arnaud Van WettereArnaud Van Wettere
Arnaud Van Wettere
Syringomyelia is a form of myelodysplasia defined by the formation of one or more fluid-filled cavities within the spinal cord that do not communicate with the central canal. The defect may be congenital or acquired. Clinical signs correlate to the segment of spinal cord affected and include pain, paresis, proprioceptive deficits, alterations in sensation, scoliosis, and autonomic dysfunction. This report describes the clinical and pathologic changes in a case of acquired syringomyelia in a 10-year-old American Paint Horse mare. The horse had a six-week history of progressive proprioceptive deficits in all four limbs, bilateral pelvic limb ataxia, and muscle fasciculations that were unresponsive to treatment with stall rest, phenylbutazone, and dexamethasone. Syringomyelia was diagnosed postmortem within cervical, thoracic, and lumbar spinal cord segments. Acquired syringomyelia should be considered among differential diagnoses in adult horses displaying progressive neurologic deficits.