Marjanović, Ana

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59 2020 - 2027
42 2010 - 2019

Mp-cat.

Date issued - custom

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Results 81-100 of 101 Results/Page

Issue Date	Title	Author(s)	Type	Мp-cat.
2018	Myotonic dystrophy type 2 as a multisystem disease	Božović, Ivo ; Perić, Stojan ; Pešović, Jovan Z. ; Bjelica, Bogdan ; Brkušanin, Miloš Đ. ; Basta, Ivana ; Marjanović, Ana ; Branković, Marija ; Kačar, Aleksandra ; Savić-Pavićević, Dušanka Lj. ; Rakočević-Stojanović, Vidosava ;	Conference Paper	Mp. category will be shown later
2018	Analysis of pathogenic mtDNA mutations associated with Leber's hereditary optic neuropathy: our experience	Dawod, Phepy Gamil Anwar; Rovčanin, Branislav ; Branković, Marija ; Marjanović, Ana ; Janković, Milena ; Novaković, Ivana ; Motaleb, Fayda Ibrahim Abdel; Jančić, Jasna ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2018	Contribution to the knowledge on the distribution of freshwater sponges – the Danube and Sava rivers case study	Anđus, Stefan ; Nikolić, Nađa ; Dobričić, Valerija ; Marjanović, Ana ; Gačić, Zoran ; Branković, Goran ; Raković, Maja ; Paunović, Momir	Article	22M22
2018	NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C	Branković, Marija ; Kresojević, Nikola D. ; Marjanović, Ana ; Novaković, Ivana V. ; Kostić, Vladimir K.	Conference Paper	Mp. category will be shown later
2018	Myotonic Dystrophy Type 2 – Data from the Serbian Registry	Božović, Ivo ; Perić, Stojan ; Pešović, Jovan ; Bjelica, Bogdan ; Brkušanin, Miloš ; Basta, Ivana ; Božić, Marija ; Senćanić, Ivan; Marjanović, Ana ; Branković, Marija ; Savić-Pavićević, Dušanka ; Rakočević-Stojanović, Vidosava ;	Article	Mp. category will be shown later
2018	C9ORF72 genetic screening in Serbian patients with neurodegenerative disorders	Marjanović, Ana ; Dobričić, Valerija S. ; Marjanović, Ivan V. ; Branković, Marija ; Janković, Milena Z ; Mandić, Gorana B. ; Stević, Zorica D. ; Novaković, Ivana V. ; Stefanova, Elka D. ; Kostić, Vladimir K.	Conference Paper	Mp. category will be shown later
2017	Study of ATXN2 repeath length in C9ORF72 expansion carriers	Marjanović, Ana ; Dobričić, Valerija ; Marjanović, Ivan ; Branković, Marija ; Janković, Milena ; Mandić, Gordana; Stefanova, Elka ; Stević, Zorica ; Novaković, Ivana ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2017	SOD1, TDP-43, FUS/TLS and C9orf72 genes in Serbian ALS patients: long term survey	Keckarević, Dušan P. ; Janković, Milena ; Gagić, Milica; Keckarević-Marković, Milica P. ; Kecmanović, Miljana M. ; Marjanović, Ana S. ; Marjanović, Ivan V. ; Novaković, Ivana V. ; Stević, Zorica D.	Conference Paper	Mp. category will be shown later
2017	Next generation sequencing in dystonia - our experience	Novaković, Ivana ; Branković, Marija ; Marjanovic, Ana ; Janković, Milena ; Dobričić, Valerija ; Stojiljković, Maja ; Petrović, Igor ; Pavlović, Sonja ; Svetel, Marina ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2017	First report of angiogenin gene mutations in patients with amyotrophic lateral sclerosis in Serbia	Janković, Milena ; Marjanović, Ivan ; Marjanović, Ana ; Perić, Stojan ; Basta, Ivana ; Novaković, Ivana ; Stević, Zorica	Conference Paper	Mp. category will be shown later
2017	The presence of premutation in the FMR1 gene in patients with clinical picture of degenerative ataxia, tremor and parkinsonism	Pešić, Milica ; Marjanović, Ana ; Radivojević, Danijela ; Ćirković, Sanja; Grk, Milka ; Dušanović-Pjević, Marija ; Novaković, Ivana ; Dobričić, Valerija ; Dragašević-Mišković, Nataša ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2017	PANK2 gene mutation spectrum in Serbian patients with neurodegeneration with brain iron accumulation	Novaković, Ivana ; Svetel, Marina ; Hartig, Monika; Dobričić, Valerija ; Janković, Milena ; Marjanović, Ana ; Branković, Marija ; Krajnović, Maja; Cvetković, Dragana ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2017	Genetic study of Achondroplasia in Serbian population	Radunović, Sara; Dobričić, Valerija ; Marjanović, Ana ; Branković, Marija ; Joksić, Ivana ; Kontić, Olivera ; Čuturilo, Goran ; Novaković, Ivana ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2017	Prospective measurement of quality of life in myotonic dystrophy type 1	Perić, Stojan Z. ; Heatwole. C.; Durovic, E; Kačar, Aleksandra S. ; Nikolić, Ana V. ; Basta, Ivana Ž. ; Marjanović, Ana S. ; Stević, Zorica ; Lavrnić, Dragana V. ; Stojanović, Vidosava M.	Article	21M21
2017	Freshwater sponges in Danube and Sava rivers – molecular and morphological identification	Anđus, Stefan P. ; Nikolić, Nađa S. ; Dobričić, Valerija ; Marjanović, Ana S. ; Raković, Maja J. ; Paunović, Momir M.	Conference Paper	Mp. category will be shown later
2017	Analysis of mtDNA mutations in Serbian patients with Lebers optic atrophy	Dawod, Phepy G. A.; Rovčanin, Branislav ; Branković, Marija ; Marjanović, Ana ; Janković, Milena ; Novaković, Ivana ; Dujmović, Irena ; Jančić, Jasna ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2017	NPC1 and NPC2 gene analysis in Serbian patients with Niemann-Pick disease type C	Branković, Marija ; Dobričić, Valerija ; Kresojević, Nikola ; Marjanović, Ana ; Novaković, Ivana ; Kostić, Vladimir	Conference Paper	Mp. category will be shown later
2016	Five-year study of quality of life in myotonic dystrophy	Perić, Stojan ; Vujnić, Milorad; Dobričić, Valerija ; Marjanović, Ana ; Basta, Ivana ; Novaković, Ivana V. ; Lavrnić, Dragana ; Rakočević-Stojanović, Vidosava	Article	21M21
2016	HPCA-related dystonia: Too rare to be found?	Dobričić, Valerija ; Kresojević, Nikola ; Marjanović, Ana ; Tomić, Aleksandra ; Svetel, Marina ; Novaković, Ivana ; Kostić, Vladimir	Article	21aM21a
2015	Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited	Dobričić, Valerija ; Kresojević, Nikola ; Žarković, Milena; Tomić, Aleksandra ; Marjanović, Ana ; Westenberger, Ana; Cvetković, Dragana ; Svetel, Marina ; Novaković, Ivana ; Kostić, Vladimir	Article	21M21