Zobrazeno 1 - 10
of 285
pro vyhledávání: '"Sofijanova, A."'
Publikováno v:
Balkan Journal of Medical Genetics, Vol 25, Iss 2, Pp 71-76 (2022)
Holoprosencephaly (HPE) is the most common embryonic forebrain developmental anomaly. It involves incomplete or absent division of the prosencephalon into two distinct cerebral hemispheres during the early stages of organogenesis. HPE is etiologicall
Externí odkaz:
https://doaj.org/article/87cc755e939243079594a31269cd0c4e
Autor:
Ridova, Nevenka, Trajkova, Sanja, Chonevska, Biljana, Stojanoski, Zlate, Ivanovski, Martin, Popova-Labachevska, Marija, Stojanovska-Jakimovska, Simona, Filipche, Venko, Sofijanova, Aspazija, Panovska-Stavridis, Irina
Publikováno v:
In Molecular Genetics and Metabolism Reports September 2022 32
Autor:
Naunova-Timovska Silvana, Sofijanova Aspazija, Bojadzieva Sonja, Shuperliska Elizabeta, Jordanova Olivera
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 150, Iss 5-6, Pp 302-307 (2022)
Introduction/Objective. This study was designed to demonstrate the association of the RIFLE classification and neutrophil gelatinase-associated lipocalin (NGAL) in predicting of newborns with acute kidney injury (AKI). Methods. This was a prospective
Externí odkaz:
https://doaj.org/article/6f6cc1fe99b04ac5b8fd8fb545695f40
Autor:
Nevenka Ridova, Sanja Trajkova, Biljana Chonevska, Zlate Stojanoski, Martin Ivanovski, Marija Popova-Labachevska, Simona Stojanovska-Jakimovska, Venko Filipche, Aspazija Sofijanova, Irina Panovska-Stavridis
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 32, Iss , Pp 100895- (2022)
The majority of Gaucher Disease (GD) cases result from pathologic mutations in the GBA1 gene. A rich mutational spectrum of about 500 identified variants has been recognized. The disease is characterized by phenotypic diversity. Data regarding the ge
Externí odkaz:
https://doaj.org/article/0642f2602258478da790e4e96a1e9e17
Publikováno v:
Clinical Case Reports, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract We report a unique case of self‐healing collodion baby (CB) that was successfully managed despite the risk of potentially serious complications. Self‐healing CB is a rare and distinct outcome of collodion phenotype occurring in approxima
Externí odkaz:
https://doaj.org/article/352d3f717fb2410086ff446ea0b3db7c
Publikováno v:
South East European Journal of Sustainable Development; 2024, Vol. 8 Issue 3, p47-51, 5p
Autor:
Nikolina Zdraveska, Aco Kostovski, Aspazija Sofijanova, Snezana Jancevska, Jana Jovanovska, Milena Kacarska, Katerina Damevska
Publikováno v:
Clinical Case Reports, Vol 10, Iss 6, Pp n/a-n/a (2022)
Abstract Neonatal lupus erythematosus (NLE) is a rare autoimmune disease due to a passive transfer of maternal autoantibodies to the fetus. The clinical spectrum is variable and includes skin lesions, cardiac, hematological, or hepatobiliary disorder
Externí odkaz:
https://doaj.org/article/dd6380dbb31f46c5bfd4f46106fac1a2
Autor:
Aleksovski, Boris, Neceva, Violeta, Vujović, Viktorija, Manusheva, Nensi, Rendevski, Vladimir, Novotni, Antoni, Filipce, Ana, Spasovska, Anastazija, Sofijanova, Aspazija, Aleksovski, Vasko, Gjorgoski, Icko
Publikováno v:
In Thrombosis Research May 2018 165:24-32
Publikováno v:
Економски Развој - Economic Development / Economic Development. 20(1-2):187-201
Externí odkaz:
https://www.ceeol.com/search/article-detail?id=674841
Autor:
Danilo Nonkulovski, Filip Duma, Aspazija Sofijanova Danilo Nonkulovski, Filip Duma, Aspazija Sofijanova, Ilija Kirovski, Ivona Jovanovska, Tafije Daci Rexhepi Ilija Kirovski, Ivona Jovanovska, Tafije Daci Rexhepi, Tanja Ignatovska, Milkica Pasoska Tanja Ignatovska, Milkica Pasoska
Publikováno v:
INTERNATIONAL JOURNAL OF INNOVATIVE MEDICINE & HEALTHCARE. :22-27
Introduction Tethered cord is a term for several different conditions. Common to all conditions of the tethered cord is that the movement of the spinal cord is limited at its base. During daily activities, the spinal cord can not move up and down ins
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80fa76c82678502bd33a084679a0e488
https://doi.org/10.55858/ijimh01022022-22
https://doi.org/10.55858/ijimh01022022-22