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Naslov Analysis of mtDNA mutations in Serbian patients with Leber hereditary optic neuropathy (Meeting Abstract)
Autori Dawod Phepy GA  Rovcanin Branislav R  Marjanovic Ana  Marjanovic Ana  Jankovic Milena Z  Novakovic Ivana V  Dujmovic Irena  Jancic Jasna B  Kostic Vladimir S 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 181-181
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov De novo mutations in idiopathic male infertility (Meeting Abstract)
Autori Hodzic Alenka  Maver Ales  Zorn Branko  Plaseska-Karanfilska Dijana  Ristanovic Momcilo  Novakovic Ivana V  Peterlin Borut 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 16-17
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Increased burden of ultra-rare genetic variants in the inflammasome regulatory genes in patients with multiple sclerosis (Meeting Abstract)
Autori Peterlin Borut  Vidmar Lovro  Drulovic Jelena S  Sepcic Juraj  Novakovic Ivana V  Ristic Smiljana  Sega-Jazbec Sasa  Maver Ales 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2019), vol. 26 br. , Suppl. 1, str. 885-885
Projekat Slovenian Research Agency
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov The pattern of inheritance and genetic status in early onset Alzheimer's disease and frontotemporal dementia (Meeting Abstract)
Autori Mandic-Stojmenovic Gorana B  Stefanova Elka D  Novakovic Ivana V  Dobricic Valerija S  Stojkovic Tanja  Kostic Vladimir K 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2019), vol. 26 br. , Suppl. 1, str. 120-120
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes (Article)
Autori Vidmar Lovro  Mayer Ales  Drulovic Jelena S  Sepcic Juraj  Novakovic Ivana V  Ristic Smiljana  Sega Sasa  Peterlin Borut 
Info SCIENTIFIC REPORTS, (2019), vol. 9 br. , str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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 ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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  
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