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Autori: Novakovic Ivana V

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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 ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Identification of mutations in the PARK2 gene in Serbian patients with Parkinson's disease (Article)
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 JOURNAL OF THE NEUROLOGICAL SCIENCES, (2018), vol. 393 br. , str. 27-30
Projekat Serbian Ministry of Science and Technological Development [ON175090, ON175091]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion (Article)
Autori Hodzic Alenka  Lavtar Polona  Ristanovic Momcilo  Novakovic Ivana V  Dotlic Jelena R  Peterlin Borut 
Info PLOS ONE, (2018), vol. 13 br. 5, str. -
Projekat Slovenian Research Agency [P3-0326]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia (Article)
Autori Dobricic Valerija S  Tomic Aleksandra D  Brankovic Vesna  Kresojevic Nikola D  Jankovic Milena Z  Westenberger Ana  Milic-Rasic Vedrana M  Klein Christine  Novakovic Ivana V  Svetel Marina V  Kostic Vladimir S 
Info PARKINSONISM & RELATED DISORDERS, (2017), vol. 45 br. , str. 81-84
Projekat Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation; German Research Foundation (DFG) Research Unit [FOR2488]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients (Article)
Autori Mitropoulos Konstantinos  ...  Dobricic Valerija S  Novakovic Ivana V  Kostic Vladimir S  ...  (broj koautora 33) 
Info HUMAN GENOMICS, (2017), vol. 11 br. , str. -
Projekat European Commission [RD-Connect] [FP7-305444]; European Commission [U-PGx] [H2020-668353]; Greek General Secretariat of Research and Technology [eMoDiA] [PiDeltaE11_0415]; Golden Helix Foundation; Serbian Ministry of Education, Science and Technology deve
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov The emerging role of the FKBP5 gene polymorphisms in vulnerability-stress model of schizophrenia: further evidence from a Serbian population (Article)
Autori Mihaljevic Marina M  Zeljic Katarina  Soldatovic Ivan A  Andric Sanja V  Mirjanic Tijana  Richards Alexander  Mantripragada Kiran  Pekmezovic Tatjana D  Novakovic Ivana V  Maric Nadja P 
Info EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, (2017), vol. 267 br. 6, str. 527-539
Projekat European Network of National Schizophrenia Networks Studying Gene-Environment Interactions -EU-GEI [HEALTH-F2-2010-241909]; Ministry of Education and Sciences of Serbia [III 41029]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis (Article)
Autori Maver Ales  ...  Drulovic Jelena S  Pekmezovic Tatjana D  Novakovic Ivana V  ...  (broj koautora 19) 
Info SCIENTIFIC REPORTS, (2017), vol. 7 br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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