Genetic Aspects of Inflammation and Immune Response in Stroke

por Nikolic, Dejan, Jankovic, Milena, Petrovic, Bojana, Novakovic, Ivana
Publicado 2020

The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti

por Minić, Snežana, Cerovac, Nataša, Novaković, Ivana, Gazikalović, Slobodan, Popadić, Svetlana, Trpinac, Dušan
Publicado 2023

Genetic variation in the CLOCK gene is associated with idiopathic recurrent spontaneous abortion

por Hodžić, Alenka, Lavtar, Polona, Ristanović, Momčilo, Novaković, Ivana, Dotlić, Jelena, Peterlin, Borut
Publicado 2018

The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options

por Jankovic, Milena, Petrovic, Bojana, Novakovic, Ivana, Brankovic, Slavko, Radosavljevic, Natasa, Nikolic, Dejan
Publicado 2022

miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome

por Jankovic, Milena, Nikolic, Dejan, Novakovic, Ivana, Petrovic, Bojana, Lackovic, Milan, Santric-Milicevic, Milena
Publicado 2023

Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation

por Minić, Snežana, Trpinac, Dušan, Novaković, Ivana, Cerovac, Nataša, Dobrosavljević Vukojević, Danijela, Rosain, Jérémie
Publicado 2022

Genetic Variation in Circadian Rhythm Genes CLOCK and ARNTL as Risk Factor for Male Infertility

por Hodžić, Alenka, Ristanović, Momčilo, Zorn, Branko, Tulić, Cane, Maver, Aleš, Novaković, Ivana, Peterlin, Borut
Publicado 2013

Associations of Common Variants in HFE and TMPRSS6 Genes with Hepcidin-25 and Iron Status Parameters in Patients with End-Stage Renal Disease

por Dopsaj, Violeta, Topić, Aleksandra, Savković, Miljan, Milinković, Neda, Novaković, Ivana, Ćujić, Danica, Simić-Ogrizović, Sanja
Publicado 2019

Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes

por Vidmar, Lovro, Maver, Ales, Drulović, Jelena, Sepčić, Juraj, Novaković, Ivana, Ristič, Smiljana, Šega, Saša, Peterlin, Borut
Publicado 2019

KCC2 rs2297201 Gene Polymorphism Might be a Predictive Genetic Marker of Febrile Seizures

por Dimitrijevic, Sanja, Jekic, Biljana, Cvjeticanin, Suzana, Tucovic, Aleksandra, Filipovic, Tamara, Novaković, Ivana, Ivić, Bojana, Nikolic, Dimitrije
Publicado 2022

Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages

por Pereza, Nina, Terzić, Rifet, Plaseska-Karanfilska, Dijana, Miljanović, Olivera, Novaković, Ivana, Poslon, Željka, Ostojić, Saša, Peterlin, Borut
Publicado 2022

Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients

por Perovic, Dijana, Damnjanovic, Tatjana, Jekic, Biljana, Dusanovic‐Pjevic, Marija, Grk, Milka, Djuranovic, Ana, Rasic, Milica, Novakovic, Ivana, Maksimovic, Nela
Publicado 2022

Association of PRDM16 rs12409277 and CtBP2 rs1561589 gene polymorphisms with lipid profile of adolescents

por Maksimovic, Nela, Vidovic, Vanja, Damnjanovic, Tatjana, Jekic, Biljana, Majkic Singh, Nada, Simeunovic, Slavko, Bozovic, Dara Savic, Vidovic, Stojko, Novakovic, Ivana
Publicado 2021

Physical activity evaluation in Yugoslav Study of the Precursors of Atherosclerosis in School Children – YUSAD study

por Simeunovic, Slavko, Milincic, Zeljka, Nikolic, Dejan, Simeunovic, Dejan, Arandjelovic, Dragana, Novakovic, Ivana, Petronic, Ivana, Risimic, Dijana, Nedeljkovic, Srecko, Vukotic, Milija
Publicado 2010

C-5 Hydroxyethyl and Hydroxypropyl Acyclonucleosides as Substrates for Thymidine Kinase of Herpes Simplex Virus Type 1 (HSV-1 TK): Syntheses and Biological Evaluation

por Meščić, Andrijana, Krištafor, Svjetlana, Novaković, Ivana, Osmanović, Amar, Müller, Ursina, Završnik, Davorka, Ametamey, Simon M., Scapozza, Leonardo, Raić-Malić, Silvana
Publicado 2013

Genetic and Epigenomic Modifiers of Diabetic Neuropathy

por Jankovic, Milena, Novakovic, Ivana, Nikolic, Dejan, Mitrovic Maksic, Jasmina, Brankovic, Slavko, Petronic, Ivana, Cirovic, Dragana, Ducic, Sinisa, Grajic, Mirko, Bogicevic, Dragana
Publicado 2021

Multidimensional aspects of pain in myotonic dystrophies

por Peric, Marina, Peric, Stojan, Rapajic, Nada, Dobricic, Valerija, Savic-Pavicevic, Dusanka, Nesic, Ivana, Radojicic, Svetlana, Novakovic, Ivana, Lavrnic, Dragana, Rakocevic-Stojanovic, Vidosava
Publicado 2015

Current Concepts on Genetic Aspects of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis

por Jankovic, Milena, Novakovic, Ivana, Gamil Anwar Dawod, Phepy, Gamil Anwar Dawod, Ayman, Drinic, Aleksandra, Abdel Motaleb, Fayda I., Ducic, Sinisa, Nikolic, Dejan
Publicado 2021

Whole Mitochondrial Genome Analysis in Serbian Cases of Leber’s Hereditary Optic Neuropathy

por Dawod, Phepy G. A., Jancic, Jasna, Marjanovic, Ana, Brankovic, Marija, Jankovic, Milena, Samardzic, Janko, Potkonjak, Dario, Djuric, Vesna, Mesaros, Sarlota, Novakovic, Ivana, Abdel Motaleb, Fayda I., Kostic, Vladimir S., Nikolic, Dejan
Publicado 2020

Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review

por Dawod, Phepy G. A., Jancic, Jasna, Marjanovic, Ana, Brankovic, Marija, Jankovic, Milena, Samardzic, Janko, Gamil Anwar Dawod, Ayman, Novakovic, Ivana, Abdel Motaleb, Fayda I., Radlovic, Vladimir, Kostic, Vladimir S., Nikolic, Dejan
Publicado 2021