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1دورية أكاديمية
المؤلفون: Ena Batinović, Anet Papazovska Cherepnalkovski, Bernarda Lozić, Luka Brajković, Ivana Zanchi, Vesna Pavlov, Marija Bucat
المصدر: Acta Medica, Vol 66, Iss 1, Pp 32-36 (2023)
مصطلحات موضوعية: Medicine
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Vesna Pavlov, Anet Papazovska Cherepnalkovski, Marino Marcic, Ljiljana Marcic, Radenka Kuzmanic Samija
المصدر: Biomedicines, Vol 11, Iss 10, p 2795 (2023)
مصطلحات موضوعية: hypoxic–ischemic encephalopathy, genetic variants, single nucleotide polymorphisms, Biology (General), QH301-705.5
وصف الملف: electronic resource
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3دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
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المصدر: Hrvatski časopis zdravstvenih znanosti
Volume 2
Issue 1مصطلحات موضوعية: deficit glukoza-6-fosfat dehidrogenaze, kvantitativno ispitivanje, referentne vrijednosti, Republika Sjeverna Makedonija, Glucose-6-phosphate dehydrogenase deficiency, quantitative testing, reference values, Republic of North Macedonia
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdbe2a5d51e648777dee0eb09798e491
https://doi.org/10.48188/hczz.2.1.6 -
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المؤلفون: Batinović, Ena, Papazovska Cherepnalkovski, Anet, Lozić, Bernarda, Brajković, Luka, Zanchi, Ivana, Pavlov, Vesna, Bucat, Marija
مصطلحات موضوعية: COVID 19, Edwards Syndrome, Klinefelter Syndrome, aneuploidy, genetic nondisjunctions
URL الوصول: https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::0005a43df9f360f49da45c7317e57ba4
https://doi.org/10.14712/18059694.2023.13 -
6دورية أكاديمية
المؤلفون: Papazovska-Cherepnalkovski A, Koceva S, Kocova M
المصدر: Balkan Journal of Medical Genetics, Vol 11, Iss 2, Pp 31-37 (2008)
مصطلحات موضوعية: karyotype, sry gene, turner syndrome, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1311-0160
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المؤلفون: Natasha Aluloska, Anet Papazovska Cherepnalkovski, Nikolina Zdraveska, Katica Piperkova, Vjekoslav Krzelj
مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, business.industry, InformationSystems_INFORMATIONSTORAGEANDRETRIEVAL, Medicine, business, The Republic, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries)
URL الوصول: 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 -
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المؤلفون: Todor Gruev, Natasa Najdanovska Aluloska, Vjekoslav Krzelj, Anet Papazovska Cherepnalkovski, Beti Zafirovska-Ivanovska, Nikolina Zdraveska, Joško Markić, Katica Piperkovska
المصدر: Open Access Macedonian Journal of Medical Sciences, Vol 3, Iss 4, Pp 694-698 (2015)
Open Access Macedonian Journal of Medical Sciences
Open Access Macedonian Journal of Medical Sciences; Vol 3, No 4 (2015): Dec 15 (OAMJMS); 694-698
Open Access Macedonian Journal of Medical Sciences; Vol. 3 No. 4 (2015): Dec 15 (OAMJMS); 694-698مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Bilirubin, unspecific etiology, lcsh:Medicine, Hematocrit, Gastroenterology, chemistry.chemical_compound, Blood serum, ABO/Rh isoimmunisation, Coombs test, Internal medicine, ABO blood group system, medicine, hemolytic jaundice, medicine.diagnostic_test, business.industry, lcsh:R, laboratory, Paediatrics, General Medicine, Clinical Science, Jaundice, chemistry, Immunology, Etiology, Medicine, Hemoglobin, medicine.symptom, business
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c15ffef7b60fb876a8f837f77a2e8df5
https://doi.org/10.3889/oamjms.2015.129 -
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المؤلفون: Papazovska Cherepnalkovski, Anet, Zemunik, Tatijana, Glamočanin, Sofijanka, Piperkova, Katica, Gunjača, Ivana, Kocheva, Svetlana, Coneska Jovanova, Biljana, Krželj, Vjekoslav
المصدر: Medical Archives
مصطلحات موضوعية: Male, Original Paper, Heterozygote, Mutation, Missense, Republic of Macedonia, genotype-phenotype correlation, Glucosephosphate Dehydrogenase, Polymerase Chain Reaction, Republic of North Macedonia, molecular characterization, Glucosephosphate Dehydrogenase Deficiency, hemic and lymphatic diseases, G6PD deficiency, Mutation, G6PD defiiency, Humans, Female, Genetic Association Studies
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المؤلفون: Алулоска (Aluloska), Наташа (Natasha), Кировски (Kirovski), Илија (Ilija), Папазовска-Черепналковски (Papazovska-Cherepnalkovski), Анет (Anet), Палчевска (Palchevska), Снежана (Snezhana), Бицевска-Манџуковска (Bicevska-Mandzukovska), Христина (Hristina), Китева-Тренчевска (Kiteva-Trenchevska), Гордана (Gordana), Тасиќ (Tasic), Велибор (Velibor)
المصدر: Archives of Public Health; Vol 9, No 2 (2017): Archives of Public Health; 5-11
Архиви на јавното здравје; Vol 9, No 2 (2017): Archives of Public Health; 5-11مصطلحات موضوعية: малформации, бубрези, уринарен тракт, клинички тек, исход, Nephrology, Medicine, Нефрологија, malformations, kidneys, urinary tract, clinical course, outcome, Медицина
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=iddesignpres::7eaf7627083ec0937f871c520ef67612
http://www.id-press.eu/aph/article/view/1358