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Peter C. Taylor

Researcher at University of Oxford

Publications -  397
Citations -  19020

Peter C. Taylor is an academic researcher from University of Oxford. The author has contributed to research in topics: Rheumatoid arthritis & Arthritis. The author has an hindex of 63, co-authored 359 publications receiving 16347 citations. Previous affiliations of Peter C. Taylor include HealthPartners & University of Cambridge.

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Metabolic profiling predicts response to anti-tumor necrosis factor α therapy in patients with rheumatoid arthritis.

TL;DR: The clear relationship between urine metabolic profiles of RA patients at baseline and their response to anti-TNF therapy may allow development of novel approaches to the optimization of therapy.
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Ofatumumab, a fully human anti-CD20 monoclonal antibody, in biological-naive, rheumatoid arthritis patients with an inadequate response to methotrexate: a randomised, double-blind, placebo-controlled clinical trial

TL;DR: Ofatumumab significantly improved all clinical outcomes in biological-naive, active rheumatoid arthritis patients with no detectable immunogenicity at week 24, and no unexpected safety findings were identified.
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Clinical efficacy of launched JAK inhibitors in rheumatoid arthritis.

TL;DR: Tofacitinib and baricitinib are the first orally available, small-molecule inhibitors of Janus kinase (JAK) enzymes to be approved for the treatment of RA and demonstrated rapid improvements in disease activity, function and patient-reported outcomes as well as disease modification.
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Antibody therapy for rheumatoid arthritis.

TL;DR: High-quality monoclonal antibodies with specificity for relevant disease molecules can now be produced in abundance and there is preliminary evidence for the clinical efficacy of both keliximab and rituximab, a chimeric mAb against the B cell antigen CD20 and CTLA4-Ig.
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Isolated left anterior descending coronary atherosclerosis: long-term comparison of internal mammary artery and venous autografts.

TL;DR: Recommendations for revascularization can be made selectively to patients with critical isolated left anterior descending stenoses who have limiting symptoms and large areas of viable myocardium at risk.