Autori: Damnjanovic Tatjana M
Naslov | Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients (Article) |
Autori | Perovic Dijana ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | JOURNAL OF CLINICAL LABORATORY ANALYSIS, (2022), vol. 36 br. 6, str. - |
Projekat | Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | TT genotype of the MMP-9-1562C/T polymorphism may be a risk factor for thrombolytic therapy-induced hemorrhagic complications after acute ischemic stroke (Article) |
Autori | Dusanovic-Pjevic Marija G ![]() ![]() ![]() ![]() ![]() ![]() |
Info | PHARMACOTHERAPY, (2021), vol. 41 br. 7, str. 562-571 |
Projekat | Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [175087, 175091]; Ministry of Education, Science and Technological Development of the Republic of Serbia [175087, 175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Analysis of association of MMP-2 gene promoter haplotype with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis (Meeting Abstract) |
Autori | Grk Milka B ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 979-979 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Analysis of the association withinMMP-2gene polymorphisms and ischemic stroke outcome after thrombolytic therapy (Meeting Abstract) |
Autori | Dusanovic-Pjevic Marija G ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 978-978 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Investigation of the MMP2 haplotype as a risk factor for the development of cerebral palsy (Meeting Abstract) |
Autori | Djuranovic Ana S ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2020), vol. 28 br. SUPPL 1, Suppl. 1, str. 351-351 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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Naslov | Association of the Brain-Derived Neurotrophic Factor Val66met Polymorphism with Body Mass Index, Fasting Glucose Levels and Lipid Status in Adolescents (Article) |
Autori | Vidovic Vanja Maksimovic Nela S ![]() ![]() ![]() ![]() ![]() ![]() |
Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2020), vol. 23 br. 1, str. 77-82 |
Projekat | Serbian Ministry of Education, Science and Technological development [175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Analysis of association of ADORA(2)A and ADORA(3) polymorphisms genotypes/haplotypes with efficacy and toxicity of methotrexate in patients with Rheumatoid arthritis (Article) |
Autori | Grk Milka B ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | PHARMACOGENOMICS JOURNAL, (2020), vol. 20 br. 6, str. 784-791 |
Projekat | Slovenian Research Agency - Slovenia [P1-0170]; Ministry of Education, Science and Technological Development of the Republic of Serbia [175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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Naslov | Genetic variant rs16944 in IL1B gene is a risk factor for early-onset sepsis susceptibility and outcome in preterm infants (Article) |
Autori | Varljen Tatjana J ![]() ![]() ![]() ![]() ![]() |
Info | INFLAMMATION RESEARCH, (2020), vol. 69 br. 2, str. 155-157 |
Projekat | Ministarstvo Prosvete, Nauke i Tehnoloskog Razvoja [~175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Methotrexate pharmacogenetics in the treatment of rheumatoid arthritis (Review) |
Autori | Jekic Biljana B ![]() ![]() ![]() |
Info | PHARMACOGENOMICS, (2019), vol. 20 br. 17, str. 1235-1245 |
Projekat | Ministry of Education, Science and Technological Development of the Republic of Serbia [175091] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Genetic variant rs16944 in IL1B gene is a risk factor for early onset sepsis susceptibility and outcome in preterm infants (Meeting Abstract) |
Autori | Maksimovic Nela S ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1364-1365 |
Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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