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Autori: Novakovic Ivana V

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Naslov Phenotypic expression and founder effect of PANK2 c.1583C > T (p.T528M) mutation in Serbian pantothenate kinase-associated neurodegeneration patients (Article)
Autori Svetel Marina V  Hartig Monika B Cvetkovic Dragana D Beaubois Cyrielle Maksic Jasmina  Novakovic Ivana V  Krajinovic Maja Kostic Vladimir K 
Info ARCHIVES OF BIOLOGICAL SCIENCES, (2019), vol. 71 br. 2, str. 275-280
Projekat Ministry of Education, Science and Technological Development of Serbia [175090]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Analysis of the Association Between Polymorphisms within PAI-1 and ACE genes and Ischemic Stroke Outcome After rt-PA Therapy (Article)
Autori Dusanovic-Pjevic Marija G  Beslac-Bumbasirevic Ljiljana Vojvodic Ljubica M Grk Milka B  Maksimovic Nela S  Damnjanovic Tatjana M  Novakovic Ivana V  Kacar Katarina Pesic Milica  Perovic Dijana  Savic Milan B Maksic Veljko Trickovic Jelena Jekic Biljana B  
Info JOURNAL OF PHARMACY AND PHARMACEUTICAL SCIENCES, (2019), vol. 22 br. , str. 142-149
Projekat Ministry of Education, Science and Technological Development of the Republic of Serbia [175091, 175087]
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Association between Tumor Necrosis Factor-alpha Promoter-308 G/A Polymorphism and Early Onset Sepsis in Preterm Infants (Article)
Autori Varljen Tatjana J  Rakic Olgica Sekulovic Gordana Jekic Biljana B  Maksimovic Nela S  Rankovic-Janevski Milica Novakovic Ivana V  Damnjanovic Tatjana M  
Info TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, (2019), vol. 247 br. 4, str. 259-264
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 Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease (Article)
Autori Dopsaj Violeta Topic Aleksandra S  Savkovic Miljan Milinkovic Neda Lj Novakovic Ivana V  Cujic Danica  Simic-Ogrizovic Sanja P 
Info DISEASE MARKERS, (2019), vol. br. , str. -
Projekat Ministry of Education, Science and Technological Development, Belgrade, Republic of Serbia [175041, 175035]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Association of C35T polymorphism in dihydrofolate reductase gene with toxicity of methotrexate in rheumatoid arthritis patients (Article)
Autori Vejnovic Dubravka Milic Vera D Popovic Branka M  Damnjanovic Tatjana M  Maksimovic Nela S  Bunjevacki Vera I  Krajinovic Maja Novakovic Ivana V  Damjanov Nemanja S Jekic Biljana B  
Info EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, (2019), vol. 15 br. 3, str. 253-257
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 Study of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndrome (Meeting Abstract)
Autori Novakovic Ivana V  Popovic-Kuzmanovic Dragana Stojanovic Ljudmila Trajkovic Vladimir S  
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 906-906
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Identification of mutations in PARK2 gene in Serbian patients with Parkinson's disease (Meeting Abstract)
Autori Jankovic Milena Z  Dobricic Valerija S Kresojevic Nikola D  Markovic Vladana V  Petrovic Igor N Svetel Marina V  Pekmezovic Tatjana D  Novakovic Ivana V  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 410-411
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C (Meeting Abstract)
Autori Brankovic Marija  Kresojevic Nikola D  Marjanovic Ana  Novakovic Ivana V  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 406-406
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov The burden of rare genetic variants in genes involved in tumor necrosis factor (TNF) signalling pathway in multiple sclerosis (MS) (Meeting Abstract)
Autori Peterlin AM Maver Ales Hodzic A Sega S Drulovic Jelena S  Novakovic Ivana V  Pekmezovic Tatjana D  Ristic S Kapovic Miljenko Peterlin B 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 400-400
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders (Meeting Abstract)
Autori Marjanovic Ana  Dobricic Valerija S Marjanovic Ivan V Brankovic Marija  Jankovic Milena Z  Mandic Gorana B Stevic Zorica D Novakovic Ivana V  Stefanova Elka D  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2018), vol. 26 br. , Suppl. S, str. 376-376
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science  
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