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R. D. Peters

Researcher at University of Toronto

Publications -  9
Citations -  1056

R. D. Peters is an academic researcher from University of Toronto. The author has contributed to research in topics: Imaging phantom & Harmonic wavelet transform. The author has an hindex of 9, co-authored 9 publications receiving 1023 citations. Previous affiliations of R. D. Peters include Women's College, Kolkata & Sunnybrook Health Sciences Centre.

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Journal ArticleDOI

Ex vivo tissue-type independence in proton-resonance frequency shift MR thermometry

TL;DR: A method of calibrating the temperature dependence of the proton‐resonance frequency is described and results are presented that indicate a tissue‐type independence, including physiological perturbations and volume magnetic susceptibility effects from geometry and orientation.
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Quantifying tissue damage due to focused ultrasound heating observed by MRI.

TL;DR: The results suggest that quantitative MR guidance of thermal coagulation therapy is feasible, and they provide information useful for designing future investigations in vivo.
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Prostate cancer: MR imaging and thermometry during microwave thermal ablation-initial experience.

TL;DR: Percutaneous interstitial microwave thermoablation of locally recurrent prostate carcinoma was continually guided with magnetic resonance (MR) imaging to derive tissue temperature change on the basis of proton-resonance shift.
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Magnetic resonance thermometry for predicting thermal damage: an application of interstitial laser coagulation in an in vivo canine prostate model.

TL;DR: Histological evaluation shows that the thermal‐injury boundary can be predicted from a threshold‐maximum temperature or an equivalent Arrhenius t43 period of 200 minutes, but it is not reliably predicted using the temperature‐time product.
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Proton-resonance frequency shift MR thermometry Is affected by changes in the electrical conductivity of tissue

TL;DR: A potential source of variation in the PRF‐shift method of thermometry is identified that manifests as a constant incremental phase shift per unit change in temperature that is independent of the echo‐time setting, when constructing temperature‐sensitive phase images from a gradient‐echo pulse sequence.