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Per Venge

Researcher at Uppsala University

Publications -  457
Citations -  34544

Per Venge is an academic researcher from Uppsala University. The author has contributed to research in topics: Eosinophil cationic protein & Eosinophil. The author has an hindex of 86, co-authored 454 publications receiving 33109 citations. Previous affiliations of Per Venge include University of Helsinki & Karolinska Institutet.

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The EvA study: aims and strategy

TL;DR: The population of the EvA study is different from other COPD study populations, since patients with current oral glucocorticoids, antibiotics and exacerbations or current smokers are excluded, such that the signals detected in the molecular analysis are due to the distinct inflammatory process of emphysema and airway disease in COPD.
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Biocompatibility of heparin-coated circuits used in cardiopulmonary bypass.

TL;DR: The lower levels of myeloperoxidase, lactoferrin and calprotectin during CPB in the HC group indicate that surface modification with end-point attached heparin enhances the biocompatibility of CPB.
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Predictors of histology, tissue eosinophilia and mast cell infiltration in Hodgkin's lymphoma--a population-based study.

TL;DR: Investigation of selected patient characteristics and genetic factors affect HL phenotype, in particular tissue eosinophilia, mast cell counts and HL histological subtype, finds few tumours, surrounded by numerous inflammatory cells.
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Eosinophil peroxidase: a new serum marker of atopy and bronchial hyper-responsiveness

TL;DR: S-EPO is a promising marker with a higher sensitivity for BHR than S-ECP or B-Eos, and further studies are needed to define the value of S- EPO when following disease activity.
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Cell surface expression of FcgammaRI (CD64) on neutrophils and monocytes in patients with influenza A, with and without complications.

TL;DR: It is concluded that neutrophil expression of CD64 and serum levels of HNL are both promising assays in the distinction between infections caused by bacteria or influenza A, whereas CD64 could identify patients with complications of their influenza A infection.