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Daniel G. Petereit

Researcher at University of Wisconsin-Madison

Publications -  77
Citations -  2948

Daniel G. Petereit is an academic researcher from University of Wisconsin-Madison. The author has contributed to research in topics: Brachytherapy & Cancer. The author has an hindex of 28, co-authored 69 publications receiving 2695 citations.

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The American Brachytherapy Society recommendations for high-dose-rate brachytherapy for carcinoma of the cervix

TL;DR: In this article, the authors present guidelines for using high-dose-rate brachytherapy in the management of patients with cervical cancer, taking into consideration the current availability of resources in most institutions.
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The adverse effect of treatment prolongation in cervical carcinoma

TL;DR: The results suggest that prolongation of treatment time is associated with decreased local control and survival in patients with cervical carcinoma, consistent with emerging data from other institutions.
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Medical Mistrust and Less Satisfaction With Health Care Among Native Americans Presenting for Cancer Treatment

TL;DR: A comparative community-based participatory research project in which newly-diagnosed cancer patients were prospectively surveyed using novel scales for medical mistrust and satisfaction with health care, and race was the only factor found to be significantly predictive of higher mistrust and lower satisfaction scores.
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Literature analysis of high dose rate brachytherapy fractionation schedules in the treatment of cervical cancer: is there an optimal fractionation schedule?

TL;DR: A dose response relationship could not be identified for either tumor control nor late tissue complications, and these findings do not necessarily question the validity of the linear quadratic model, as much as they question the quality of the current HDR brachytherapy literature.
Journal Article

Comparative analysis of cervical cancer in women and in a human papillomavirus-transgenic mouse model: identification of minichromosome maintenance protein 7 as an informative biomarker for human cervical cancer.

TL;DR: The mouse model was used to identify minichromosome maintenance protein 7 (MCM7), an E2F-induced cellular DNA replication factor, as a novel biomarker for cervical cancer, and strong, full thickness staining for MCM7 was seen selectively in the epithelium of high-grade intraepithelial lesions and in frank cancer.