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Vox Sanguinis|November 3, 2023
Frequency of red blood cell transfusions in preterm neonates in Brazil: A systematic review and meta-analysisCristina Ortiz Sobrinho Valete, Esther Angelica Luiz Ferreira, Carolina Perez Montenegro, et al.
Journal of Interventional Cardiology|November 28, 2019
Impact of the Balloon Inflation Time and Pattern on the Coronary Stent ExpansionJarosław Skowroński, Rafał Wolny, Jan Jastrzębski, et al.
American Heart Journal|March 30, 2006
Intravascular ultrasound assessment of the spatial distribution of ruptured coronary plaques in the left anterior descending coronary arteryJerzy Pregowski, Pawel Tyczynski, Gary S Mintz, et al.
Archives of Medical Science : AMS|February 2, 2012
Transapical aortic valve implantation - a rescue procedure for patients with aortic stenosis and "porcelain aorta"Katarzyna Czerwinska, Ewa Orłowska-Baranowska, Adam Witkowski, et al.
Kidney & Blood Pressure Research|September 24, 2004
Characterization of glucose uptake by cultured rat podocytesBarbara Lewko, Ewa Bryl, Jacek M Witkowski, et al.
Kardiologia Polska|July 1, 2004
Chronic heart failure. The relationship between increased activity of skeletal muscle ergoreceptors and reduced exercise toleranceAgnieszka Kaczmarek, Ewa A Jankowska, Tomasz Witkowski, et al.
Journal of General Internal Medicine|November 7, 2009
Adverse drug event rates in six community hospitals and the potential impact of computerized physician order entry for preventionBalthasar L Hug, Daniel J Witkowski, Colin M Sox, et al.
European Journal of Heart Failure|February 5, 2009
Pathophysiological and clinical relevance of simplified monitoring of nocturnal breathing disorders in heart failure patientsGian Domenico Pinna, Roberto Maestri, Andrea Mortara, et al.
The American Journal of Cardiology|February 16, 2013
Prevalence and characteristics of coronary anomalies originating from the opposite sinus of Valsalva in 8,522 patients referred for coronary computed tomography angiographyMaksymilian P Opolski, Jerzy Pregowski, Mariusz Kruk, et al.
The Journal of Clinical Investigation|January 1, 1989
Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasiaE R McCabe, J Towbin, J Chamberlain, et al.
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