Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Katica Piperkova"'
Publikováno v:
Hrvatski časopis zdravstvenih znanosti
Volume 2
Issue 1
Volume 2
Issue 1
Glucose-6-phosphate dehydrogenase is a key regulatory enzyme in the pentose-phosphate cycle that participates in the formation of reduced equivalents to maintain the cellular redox status. The G6PD enzyme activity is crucial in protecting cells from
Autor:
Natasha Aluloska, Anet Papazovska Cherepnalkovski, Nikolina Zdraveska, Katica Piperkova, Vjekoslav Krzelj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f59b6f7f1f5ff7d94109c9a625e01d46
http://www.intechopen.com/articles/show/title/neonatal-hyperbilirubinemia-in-newborns-of-the-republic-of-north-macedonia
http://www.intechopen.com/articles/show/title/neonatal-hyperbilirubinemia-in-newborns-of-the-republic-of-north-macedonia
Publikováno v:
Macedonian Journal of Medical Sciences (Archived); Vol. 5 No. 4 (2012): Dec 15 (MJMS); 416-422
Macedonian Journal of Medical Sciences; Vol 5, No 4 (2012): Dec 15 (MJMS); 416-422
Macedonian Journal of Medical Sciences; Vol 5, No 4 (2012): Dec 15 (MJMS); 416-422
Background: The aim was to investigate whether S100 in serum is a prognostic marker of cerebral injury in term newborn infants with hypoxic ischemic encephalopathy (HIE) after perinatal asphyxia. Material and Methods: All risk neonates with severe as
Autor:
Svetlana Kocheva, Sofijanka Glamocanin, Katica Piperkova, Anet Papazovska Cherepnalkovski, Vjekoslav Krzelj, Biljana Coneska Jovanova, Ivana Gunjača, Tatijana Zemunik
Publikováno v:
Medical Archives. 69:284
Glucose-6-phospahte dehydrogenase deficiency (G6PD) is one of the most common inherited disorders affecting around 400 million people worldwide. Molecular analysis of the G6PD gene identified more than 140 distinct mutations, the majority being singl
Autor:
Bernarda Lozić, Todor Gruev, Ana Kuzmanić Skelin, Eugenija Marušić, Anet Papazovska Cherepnalkovski, Katica Piperkova, Vjekoslav Krzelj
Publikováno v:
Acta Informatica Medica
Background: Neonatal hyperbilirubinemia is a common clinical manifestation of the inherited glucose-6-phosphate dehydrogenase (G6PD) deficiency. Aim of the study: The aim of this study was to investigate the influence of the inherited G6PD deficiency
Publikováno v:
Early Human Development. 86:S138-S139
Autor:
Snezana Palcevska Kocevska, Anet Papazovska Cherepnalkovski, Natasa Najdanovska Aluloska, Katica Piperkova, Arijeta Hasani, Vedran Stojanovic, Gabriela Tavcioska, Ljiljana Pota
Publikováno v:
Early Human Development. 86:S141
Autor:
Ljiljana Pota, Natasa Najdanovska Aluloska, Snezana Palcevska Kocevska, Nikolina Zdravevska, Katica Piperkova, Anet Papazovska Cherepnalkovski
Publikováno v:
Early Human Development. 86:S138
Autor:
Ljiljana Kojic, Katerina Dimovska, Sonja Bojadzieva, Aspazija Sofijanova, Natasha Aluloska, Radica Muratovska, Aleksandar Sajkovski, Simonida Spasevska, Katica Piperkova
Publikováno v:
Early Human Development. 86:S81
Publikováno v:
Early Human Development. 84:S119