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Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|May 27, 2016
Effects of body temperature on post-anoxic oxidative stress from the perspective of postnatal physiological adaptive processes in ratsH Kletkiewicz, J Rogalska, A Nowakowska, et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology|February 4, 2014
Decrease in 3-nitrotyrosine in the amniotic fluid of women with cytomegalovirus infectionZ Gaj, J Wilczynski, A Nowakowska-Glab, et al.
Biomed Research International|June 21, 2014
The analysis of genetic aberrations in children with inherited neurometabolic and neurodevelopmental disordersKrystyna Szymańska, Krzysztof Szczałuba, Agnieszka Lugowska, et al.
Problemy Medycyny Wieku Rozwojowego|January 1, 1981
[Progress in the early detection of inborn errors of metabolism]K Bozkowa, B Cabalska, N Duczyńska, et al.
Optics Express|May 4, 2016
Nitride superluminescent diodes with broadened emission spectrum fabricated using laterally patterned substrateA Kafar, S Stanczyk, M Sarzynski, et al.
Journal of Applied Genetics|August 20, 2010
Prostaglandin-endoperoxide synthase genes COX1 and COX2 - novel modifiers of disease severity in cystic fibrosis patientsK Czerska, A Sobczynska-Tomaszewska, D Sands, et al.
BMC Cancer|February 11, 2024
Identification and characterization of stromal-like cells with CD207+/low CD1a+/low phenotype derived from histiocytic lesions - a perspective in vitro model for drug testingAgnieszka Śmieszek, Klaudia Marcinkowska, Zofia Małas, et al.
Neonatology|January 24, 2015
High-Resolution Array Comparative Genomic Hybridization Utility in Polish Newborns with Isolated Cleft Lip and PalateKrzysztof Szczałuba, Beata A Nowakowska, Katarzyna Sobecka, et al.
Ginekologia Polska|January 15, 2021
Prenatal diagnosis of glutaric acidemia type 2 with the use of exome sequencing - an up-to-date review and new case reportAnna M Kucinska-Chahwan, Tomasz Roszkowski, Maciej Geremek, et al.
European Journal of Human Genetics : EJHG|August 19, 2010
Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein-Taybi syndrome detected by aCGHAnne Chun-Hui Tsai, Cherilyn J Dossett, Carol S Walton, et al.
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