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A congenital defect of the pericardium.
Surgical correction of pericardial defects is concluded to be justified in patients with clinical symptoms and when they are large the said defects do not require any treatment.
Gene therapy of coronary artery disease with phvegf165--early outcome.
Direct myocardial administration of genes encoding VEGF165 can be an effective method of treatment in patients with chronic and advanced CAD either as a supplementary treatment or as a single therapy.
Protective influence of pretreatment with allopurinol on myocardial function in patients undergoing coronary artery surgery.
0,1 & 2 - three RobIn Heart prototypes comparison and tests results
Histamine metabolism in experimental silicosis. I. Experiments on the isolated rat lung and on guinea pig lung homogenates and sections.
The lack of hyperacute xenogeneic heart transplant rejection in a human.
Improved biocompatibility of extracorporeal circulation by the use of auto-oxygenation instead of artificial oxygenator in perfusion circuit.
- A. Bochenek, Z. Religa, T. Spyt
- Medicine, EngineeringNephrology, dialysis, transplantation : official…
The current study clearly confirms the superior biocompatibility of cardiopulmonary bypass with lung over oxygenator with no change in platelet count or platelet aggregation to ADP.
The use of flow cytometry for the investigation of viability of heart valve-derived fibroblasts.
The first and middle stages of spermiogenesis in Chara vulgaris are focused on, with the main proteins taking part in the reorganisation of chromatin structure and in the exchange of somatic proteins into generative ones are formed.
Electrophysiologic properties of transplanted human heart with and without rejection.
Six male heart transplant recipients underwent routine electrophysiologic evaluation and prolongation of effective refractory period of the donor atrium, functional refractoriness of the atrioventricular node, and effective refraction of the right ventricle were observed.
Coarctation of the aorta with right aortic arch. A rare case and atypical clinical picture.
- M. Szkutnik, Z. Religa, J. Białkowski, M. Wojtalik
- Medicine, EngineeringTexas Heart Institute journal
The case of a 13-year-old girl with a diffusely hypoplastic right aortic arch, anomalous origin of the left subclavian artery, and a small, insignificant ventricular septal defect is reported, which resulted in an atypical clinical picture and delayed diagnosis.