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Last year, Unilever’s Simple Skincare ushered micellar cleansing water into mass with great success. This year, it is adding cleansing oil. read more
Is the radial artery a viable conduit in coronary surgery? This study examined very-long-term outcomes in patients who received an RA graft for myocardial revascularization. Journal of the American ...
The technique uses an artery in the wrist to explore and treat the heart as opposed to an artery in the groin.
Shockwave Medical has secured approval from the US Food and Drug Administration (FDA) for its Lithoplasty system to treat calcified plaque in peripheral artery disease (PAD) patients.
W. L. Gore & Associates has received approval from the US Food and Drug Administration (FDA) for its Tigris dual-component vascular stent to treat peripheral artery disease (PAD).
The merits of PCI vs. coronary bypass graft surgery for stable coronary artery disease continue to be debated. This review examines the many factors that inform the decision-making process. European...
Okanagan Specialty Fruits' Arctic Fuji has received mostly positive public comments supporting the approval of the biotech no -More-
Various Locator abutments and attachments are available commercially for use in overdenture patients. Patients are advised to use cleansing agents to keep their overdentures clean. The effect of diffe...
Coronary artery bypass grafting with aortic valve replacement (AVR) or mitral valve replacement (MVR) is traditionally performed via sternotomy. Minimally invasive coronary surgery (MICS) and minimall...
In severe cases of epistaxis, in spite of several procedures described in the literature for its management, surgical treatment has been recognized by most authors as 1 of the most effective, especial...
As arterial myocardial revascularization is proved to provide great results, radial artery use as a graft and its consequences remain an important issue.
The history of intragastric balloons (IGBs) began in 1985 with the Garren-Edwards Bubble. It was approved by the U.S. Food and Drug Administration (FDA) for temporary use as a weight loss device, but ...