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Резултати

Prenatal diagnosis of Saethre-Chotzen syndrome caused by TWIST1 microdeletion and complex chromosomal rearrangement involving chromosomes 5, 7 and 11   [2023]

Joksić, Ivana  ; Toljić, Mina  ; Maksimović, Nela  ; Perović, Dijana  ; Jurišić, Aleksandar  

The G894T polymorphism of the eNOS gene and atherosclerosis precursors in Serbian child population   [2007]

Damnjanović, Tatjana  ; Novaković, Ivana  ; Bunjevački, Vera  ; Nedeljković, S.; Vukotić, M.; Simeunović, Slavko ; Luković, Ljiljana 

Unravelling phenylalanine-induced neuronal dysfunction: transcriptome analysis of NT2-derived neurons highlights neurite impairment and synaptic connectivity   [2025]

Stankovic, Sara; Lazic, Andrijana  ; Parezanovic, Marina V; Andjelkovic, Marina Z; Ugrin, Milena M; Stevanovic, Milena J  ; Pavlovic, Sonja T; Stojiljkovic, Maja M; Klaassen, Kristel M

Applications of the new tool: VUS Notifier   [2025]

Domazet, Milan; Ugrin, Milena M; Andjelkovic, Marina Z; Klaassen, Kristel M; Skakic, Anita G  ; Komazec, Jovana; Spasovski, Vesna M  ; Todorovic, Sasa; Stojiljkovic, Maja M

Association of ADARB1 gene with suicide attempt risk in patients with major psychiatric disorders   [2015]

Karanović, Jelena  ; Saša Šviković; Maja Pantović; Svetlana Đurica; Brajušković, Goran  ; Damjanović, Aleksandar ; Jovanović, Vladimir  ; Ivković, Maja  ; Stanka Romac; Savić-Pavićević, Dušanka  

case-control study of association of FV HR2 6775A > G polymorphisms with thrombosis in Montenegrin patients; Haplotype analysis between FV 1691G > A and FV HR2 6775A > G polymorphisms   [2024]

Teofilov, Sladjana; Miljanovic, Olivera; Ostojic, Tatjana; Bulatovic, Milena; Perovic, Sasa; Djordjevic, Natasa  

Analysis of ATXN1 and ATXN2 repeat length in C9ORF72 expansion carriers   [2019]

Marjanović, Ana ; Dobričić, Valerija S. ; Branković, Marija  ; Janković, Milena Z. ; Mandić, Gorana B.  ; Stefanova, Elka D. ; Stević, Zorica D. ; Novaković, Ivana V.  ; Kostić, Vladimir S. 

RTL in peripheral blood of CD patients as a potential predictor of the disease outcome   [2024]

Stevanović, Bojana  ; Milovanović, Ivan  ; Kosić, Marija  ; Popović, Branka  

Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier   [2022]

Kristel Klaassen  ; Đorđević, Maja; Skakić, Anita  ; Božica Kecman; Parezanović, Marina  ; Anđelković, Marina  ; Stevanović, Nina  ; Spasovski, Vesna  ; Ugrin, Milena  ; Drmanac, Radoje;
Pavlović, Sonja  ; Stojiljković, Maja  ;

Loss-of-function of AMFR causes autosomal recessive hereditary spastic paraplegia by altering lipid metabolism   [2023]

Deng, Ruizhi; ...; Capo, Ivan Dj  ; ...; (broj, koautora 27)

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