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Armen Yuri Gasparyan

Researcher at Dudley Group NHS Foundation Trust

Publications -  139
Citations -  5595

Armen Yuri Gasparyan is an academic researcher from Dudley Group NHS Foundation Trust. The author has contributed to research in topics: Medicine & Publishing. The author has an hindex of 35, co-authored 122 publications receiving 4370 citations. Previous affiliations of Armen Yuri Gasparyan include Medical University of Graz & University of Birmingham.

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Mean Platelet Volume: A Link Between Thrombosis and Inflammation?

TL;DR: Evidence, particularly derived from prospective studies and a meta-analysis, suggest a correlation between an increase in MPV and the risk of thrombosis, and MPV as a prognostic and therapeutic marker as well as the factors influencing its measurement is considered.
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Writing a narrative biomedical review: considerations for authors, peer reviewers, and editors

TL;DR: The aim of this review is to analyze the main steps in writing a narrative biomedical review and to consider points that may increase the chances of success.
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The Platelet-to-Lymphocyte Ratio as an Inflammatory Marker in Rheumatic Diseases

TL;DR: Accumulating evidence suggests that PLR can provide valuable information to clinicians who encounter multisystem manifestations of rheumatic diseases, which are reflected in shifts in platelet, lymphocyte, neutrophil, or monocyte counts.
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The Role of Aspirin in Cardiovascular Prevention: Implications of Aspirin Resistance

TL;DR: The clinical implications of aspirin resistance are explored in various cardiovascular disease states, including diabetes mellitus, hypertension, heart failure, and other similar disorders where platelet reactivity is enhanced.
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Rheumatologists' perspective on coronavirus disease 19 (COVID-19) and potential therapeutic targets.

TL;DR: Patients with coronavirus disease 19 (COVID-19) may have features mimicking rheumatic diseases, such as arthralgias, acute interstitial pneumonia, myocarditis, leuc Openia, lymphopenia, thrombocytopenia and cytokine storm with features akin to secondary hemophagocytic lymphohistiocytosis.