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American Journal of Rhinology|March 1, 1997
Correlation of middle meatal and maxillary sinus cultures in acute maxillary sinusitisA M Vaidya, J M Chow, J A Stankiewicz, et al.
Pneumonologia I Alergologia Polska|January 1, 1997
[Disruption of the middle bronchus]J Wójcik, T Grodzki, J Alchimowicz, et al.
Journal of Cataract and Refractive Surgery|September 29, 2009
Comparison of torsional and longitudinal modes using phacoemulsification parametersMarek Rekas, Robert Montés-Micó, Karolina Krix-Jachym, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|July 7, 2018
Beneficial effect of combined spironolactone and quinapril treatment on thrombosis and hemostasis in 2K1C hypertensive ratsA Gromotowicz-Poplawska, A Stankiewicz, J Mikita, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|August 6, 2002
Maxillary sinus puncture and culture in the diagnosis of acute rhinosinusitis: the case for pursuing alternative culture methodsMichael S Benninger, Peter C Appelbaum, James C Denneny, et al.
International Journal of Endocrinology|December 14, 2011
The Role of -786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic SyndromeBlazej Misiak, Marta Krolik, Anna Kukowka, et al.
Antimicrobial Agents and Chemotherapy|May 19, 2000
A novel complex mutant beta-lactamase, TEM-68, identified in a Klebsiella pneumoniae isolate from an outbreak of extended-spectrum beta-lactamase-producing KlebsiellaeJ Fiett, A Pałucha, B Miaczyńska, et al.
Klinika Oczna|March 31, 2004
[Genetic instability in human malignant uveal melanomas]Ewa Proniewska-Skretek, Witold Pepiński, Małgorzata Skawrońska, et al.
American Journal of Medical Genetics. Part A|March 22, 2005
Congenital diaphragmatic hernia in WAGR syndromeD A Scott, M L Cooper, P Stankiewicz, et al.
Human Genetics|September 15, 2005
Molecular analysis of a constitutional complex genome rearrangement with 11 breakpoints involving chromosomes 3, 11, 12, and 21 and a approximately 0.5-Mb submicroscopic deletion in a patient with mild mental retardationKatarzyna Borg, Paweł Stankiewicz, Ewa Bocian, et al.
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