Novaković, Ivana

Type

Date issued

389 2000 - 2027
3 1900 - 1999

Mp-cat.

187 М30/М60
47 M21
45 M22
38 M23
17 M21a
15 M10/M40
11 M20/M50
11 other
9 M21a+
4 M24
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Results 61-80 of 392 Results/Page

Issue Date	Title	Author(s)	Type	Мp-cat.
2023	The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti	Minić, Snežana B. ; Cerovac, Nataša M. ; Novaković, Ivana V. ; Gazikalović, Slobodan; Popadić, Svetlana P. ; Trpinac, Dušan P.	Article	21M21
2023	miRNAs as a Potential Biomarker in the COVID-19 Infection and Complications Course, Severity, and Outcome	Janković, Milena ; Nikolić, Dejan ; Novaković, Ivana ; Petrović, Bojana ; Lacković, Milan ; Šantrić-Milićević, Milena	Article	21M21
2023	Novel GATOR1 variants in focal epilepsy	Kovačević, Maša ; Janković, Milena ; Branković, Marija ; Milićević, Ognjen ; Novaković, Ivana ; Sokić, Dragoslav ; Ristić, Aleksandar ; Shamsani, Jannah; Vojvodić, Nikola	Article	22M22
2023	Motor neuron involvement in facial muscles as characteristic of ANO10 mutation	Dragašević-Mišović, Nataša ; Milovanović, Andona ; Stanković, Iva ; Marjanović, Ana ; Branković, Marija ; Dobričić, Valerija S. ; Petrović, Igor N. ; Svetel, Marina V. ; Novaković, Ivana ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2023	Clinical and genetic features of Huntington’s disease patients from Serbia: A single-center experience	Kresojević, Nikola ; Perović, Ivana; Stanković, Iva ; Tomić, Aleksandra ; Ječmenica-Lukić, Milica ; Marković, Vladana ; Stojković, Tanja ; Mandić, Gorana ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Novaković, Ivana ; Petrović, Igor ; Dragašević, Nataša ; Stefanova, Elka ; Svetel, Marina ; Kostić, Vladimir ;	Article	21M21
2023	TREM2 R47H as a risk factor for Alzheimer's disease in Serbian patients	Pešić, Milica ; Andrejić, Nikola; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka	Conference Paper	Mp. category will be shown later
2023	The association of R47H variant in the TREM2 gene and genetic susceptibility to Alzheimer's disease in Serbian population	Andrejić, Nikola; Pešić, Milica ; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Mandić, Gorana ; Novaković, Ivana ; Stojković, Tanja ; Stefanova, Elka	Article	53M53
2023	Reply to: “Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism”	Kresojević, Nikola ; Marković, Vladana ; Dobričić, Valerija ; Stanković, Iva ; Stojković, Tanja ; Tomić, Aleksandra ; Ječmenica-Lukić, MIlica ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Novaković, Ivana ; Petrović, Igor ; Dragašević, Nataša ; Svetel, Marina ; Kostić, Vladimir ;	Article	21a+M21a+
2022	Analysis of “clinical exome” panel in Serbian patients with cognitive disorders	Branković, Marija ; Stefanova, Elka ; Mandić, Gorana ; Marjanović, Ana ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Stević, Zorica ; Janković, Milena ; Novaković, Ivana ; Peterlin, Borut; Kostić, Vladimir ;	Article	22M22
2022	The Genetic Basis of Strokes in Pediatric Populations and Insight into New Therapeutic Options	Janković, Milena ; Petrović, Bojana ; Novaković, Ivana ; Branković, Slavko ; Radosavljević, Nataša ; Nikolić, Dejan	Article	21M21
2022	C9ORF72 repeat expansion is not associated with atypical parkinsonism in the Serbian population	Marjanović, Ana ; Dobričić, Valerija ; Ječmenica-Lukić, Milica ; Stanković, Iva ; Milićević, Ognjen ; Dragašević-Mišković, Nataša ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Svetel, Marina ; Stefanova, Elka ; Kostić, Vladimir ;	Article	22M22
2022	Impact of the Fetuin Gene Polymorphisms in Coronary Artery Calcification and Mortality of Patients with Chronic Kidney Disease and Renal Transplant	Jovičić-Pavlović, Svetlana; Simić-Ogrizović, Sanja P. ; Bukumirić, Zoran M. ; Erić, Milena; Pavlović, Natalija; Kotlica, Boba ; Novaković, Ivana V.	Article	22M22
2022	Phenotypic and Genetic Heterogeneity of Adult Patients with Hereditary Spastic Paraplegia from Serbia	Perić, Stojan ; Marković, Vladana ; Candayan, Ayse; De Vriendt, Els; Momčilović, Nikola; Savić, Andrija; Dragašević-Mišković, Nataša ; Svetel, Marina ; Stević, Zorica ; Božović, Ivo ; Mesaroš, Šarlota ; Drulović, Jelena ; Basta, Ivana ; Petrović, Igor ; Tamaš, Olivera; Mijajlović, Milija ; Novaković, Ivana ; Sokić, Dragoslav ; Jordanova, Albena;	Article	21M21
2022	Genetic and phenotypic variability in adult patients with Niemann Pick type C from Serbia: single-center experience	Kresojević, Nikola ; Dobričić, Valerija ; Ječmenica-Lukić, Milica ; Tomić, Aleksandra ; Petrović, Igor ; Dragašević, Nataša ; Perović, Ivana; Marjanović, Ana ; Branković, Marija ; Janković, Milena ; Novaković, Ivana ; Svetel, Marina ; Kostić, Vladimir S. ;	Article	21aM21a
2022	Clinical exome sequencing in Serbian patients with movement disorders – Single centre experience	Branković, Marija ; Dragašević, Nataša ; Dobričić, Valerija ; Maver, Aleš; Bergant, Gaber; Petrović, Igor ; Perić, Stojan ; Marjanović, Ana ; Janković, Milena ; Jančić, Jasna ; Novaković, Ivana ; Peterlin, Borut; Svetel, Marina ; Kostić, Vladimir ;	Article	22M22
2022	Current State of Compulsory Basic and Clinical Courses in Genetics for Medical Students at Medical Faculties in Balkan Countries With Slavic Languages	Pereza, Nina; Terzic, Rifet; Plaseska-Karanfilska, Dijana; Miljanovic, Olivera; Novaković, Ivana V. ; Poslon, Zeljka; Ostojic, Sasa; Peterlin, Borut	Article	21M21
2022	Correlation between leukocyte-platelet aggregates and thrombosis in myeloproliferative neoplasms	Šefer, Dijana ; Miljić, Predrag ; Kraguljac-Kurtović, Nada ; Bižić-Radulović, Sandra; Bogdanović, Andrija ; Knežević, Vesna; Marković, Dragana ; Beleslin-Čokić, Bojana ; Novaković, Ivana ; Marinković, Jelena ; Leković, Danijela ; Gotić, Mirjana ; Čokić, Vladan ;	Article	22M22
2022	Diagnostic yield of whole exome sequencing in early-onset and familial Parkinson's disease in the Balkans	Maver, Aleš; Kovanda, Anja; Bergant, Gaber; Teran, Nataša; Vrečar, Irena; Branković, Marija ; Janković, Milena Z. ; Svetel, Marina V. ; Kostić, Vladimir S. ; Novaković, Ivana V. ; Rački, Valentino; Vuletić, Vladimira; Peterlin, Borut;	Conference Paper	Mp. category will be shown later
2022	Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients	Perović, Dijana ; Damnjanović, Tatjana M. ; Jekić, Biljana B. ; Dušanović-Pjević, Marija G. ; Grk, Milka B. ; Đuranovic, Ana S. ; Rašić, Milica ; Novaković, Ivana V. ; Maksimović, Nela S.	Article	22M22
2022	Challenges in Rare Diseases Diagnostics: Incontinentia Pigmenti with Heterozygous GBA Mutation	Minić, Snežana B. ; Trpinac, Dušan P. ; Novaković, Ivana V. ; Cerovac, Nataša M. ; Dobrosavljević-Vukojević, Danijela ; Rosain, Jeremie	Article	21M21