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Julie M. Hasenwinkel

Researcher at Syracuse University

Publications -  37
Citations -  675

Julie M. Hasenwinkel is an academic researcher from Syracuse University. The author has contributed to research in topics: Bone cement & Spinal cord injury. The author has an hindex of 13, co-authored 36 publications receiving 615 citations. Previous affiliations of Julie M. Hasenwinkel include State University of New York System & Northwestern University.

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A theoretical and experimental analysis of polymerization shrinkage of bone cement: A potential major source of porosity

TL;DR: The results of this study show that shrinkage of bone cement under certain constrained conditions may result in the development of porosity at the implant-bone cement interface and elsewhere in the polymerizing cement mantle.
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A novel high-viscosity, two-solution acrylic bone cement: effect of chemical composition on properties.

TL;DR: Most compositions had exotherms, setting times, and maximum strains within the range of commercial cements and flexural strengths and moduli up to 54 and 43% higher than Simplex-P, respectively.
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Effect of initiation chemistry on the fracture toughness, fatigue strength, and residual monomer content of a novel high-viscosity, two-solution acrylic bone cement.

TL;DR: Evaluating the effect of BPO and DMPT concentrations, along with their molar ratio, on the fracture toughness, fatigue strength, and residual monomer content of the experimental compositions showed that fracture toughness and fatigue strength for the solution cements were comparable to Simplex P and were not significantly affected by the BPO concentration or the B PO:DMPT molar ratios.
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Mechanical characterization of the injured spinal cord after lateral spinal hemisection injury in the rat.

TL;DR: The results of this study show that the injured spinal tissue displays complex viscoelastic behavior, likely indicating changes in tissue permeability and diffusivity.
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Raman spectroscopic investigation of spinal cord injury in a rat model.

TL;DR: Analysis of difference spectra indicated the presence of carbonyl containing compounds, hypothesized to be products of lipid peroxidation and acid catalyzed hydrolysis of glycosaminoglycan moieties, which compared well with in vitro experiments conducted on chondroitin sulfate sugars.