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John B. Simpson

Researcher at Sequoia Hospital

Publications -  62
Citations -  4312

John B. Simpson is an academic researcher from Sequoia Hospital. The author has contributed to research in topics: Atherectomy & Angioplasty. The author has an hindex of 27, co-authored 62 publications receiving 4260 citations. Previous affiliations of John B. Simpson include University of Washington & Iowa State University.

Papers
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Journal ArticleDOI

Percutaneous transluminal coronary angioplasty: report of complications from the National Heart, Lung, and Blood Institute PTCA Registry.

TL;DR: The results support the relative safety of PTCA as a method of nonsurgical myocardial revascularization in carefully selected patients and nonfatal complications were significantly influenced by the presence of unstable angina and initial lesion severity > 90% diameter stenosis.
Journal ArticleDOI

Proliferation in primary and restenotic coronary atherectomy tissue. Implications for antiproliferative therapy.

TL;DR: The response to injury in existing animal models of angioplasty may follow a very different course of events from the clinical reality in human atherosclerotic coronary arteries and may help explain why current approaches to restenosis therapy have been ineffective.
Patent

Adjustable treatment chamber catheter

TL;DR: In this paper, a catheter device for treatment of disease in biological conduits is described, which has inner and outer coaxial catheter members, each having an inflatable balloon attached near its distal end.
Patent

Atherectomy device and method

TL;DR: In this article, an atherectomy device for removing stenosis materials from a vascular vessel is described, which includes a flexible tubular member, a flexible drive means disposed within the tubular part, and a cutting assembly carried by the distal extremity of the tube.
Journal ArticleDOI

Osteopontin is synthesized by macrophage, smooth muscle, and endothelial cells in primary and restenotic human coronary atherosclerotic plaques.

TL;DR: Using in situ hybridization and immunohistochemical methods, it is demonstrated that in addition to macrophages, smooth muscle and endothelial cells synthesize OPN mRNA and protein in human coronary atherosclerotic plaque specimens obtained by directional atherectomy, suggesting that OPN may contribute to cellular accumulations and dystrophic calcification in atherosclerosis plaques.