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Резултати

Genetic evaluation of newborns with critical congenital heart defects admitted to the intensive care unit (✓)   [2021]

Miletić, Aleksandra; Ruml-Stojanović, Jelena ; Parezanović, Vojislav  ; Rsovac, Snežana; Drakulić, Danijela  ; Soldatović, Ivan  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Borlja, Nikola;
Milivojević, Milena  ; Marjanović, Ana  ; Branković, Marija  ; Čuturilo, Goran  ;

Voiding Cystourethrography - Do We Over-Do IT   [2017]

Zivkovic, Dragana  ; Sarac, Dragan; Fratric, Ivana  

Changes in the incidence and etiology of congenital hypothyroidism detected during 30 years of a screening program in central Serbia   [2016]

Mitrovic, Katarina; Vukovic, Rade M; Milenkovic, Tatjana; Todorovic, Sladjana; Radivojcevic, Jovana; Zdravkovic, Dragan S

Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia (✓)   [2021]

Raičević, Maja; Milenković, Tatjana; Hussain, Khalid; Đorđević, Maja  ; Martić, Jelena  ; Todorović, Slađana; Mitrović, Katarina; Sarajlija, Adrijan  ; Vuković, Rade

Hypertensive encephalopathy as a late complication of autonomic dysreflexia in a 12-year-old boy with a previous spinal cord injury (✓)   [2014]

Bjelaković, Bojko  ; Dimitrijević, Lidija  ; Lukić, Stevo  ; Golubovic, Emilija 

Predictive genetic markers of coagulation, inflammation and apoptosis in Perthes disease-Serbian experience   [2015]

Srzentić Dražilov, Sanja  ; Nikčević, Gordana  ; Spasovski, Duško  ; Baščarević, Zoran  ; Živković, Zorica; Terzić-Šupić, Zorica  ; Matanović, Dragana  ; Đorđević, Valentina  ; Pavlović, Sonja  ; Spasovski, Vesna  

4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome   [2011]

Čuturilo, Goran  ; Menten, Björn; Krstic, Aleksandar; Drakulić, Danijela  ; Jovanović, Ida ; Parezanović, Vojislav  ; Stevanović, Milena  

Genotype phenotype correlation in a pediatric population with antithrombin deficiency (✓)   [2019]

Kovač, Mirjana ; Mitić, Gorana  ; Đilas, Iva ; Kuzmanović, Miloš  ; Šerbić, Olivera  ; Leković, Danijela  ; Tomić, Branko  ; Bereczky, Zsuzsanna

Primary Budd-Chiari syndrome in a 3-year-old boy with homozygous factor V Leiden G1691A mutation   [2014]

Boskovic, Aleksandra; Kitic, Ivana; Stankovic, Ivica; Prokic, Dragan; Zlatar, Nada

Three siblings with triple A syndrome with a novel frameshift mutation in the AAAS gene and a review of 17 independent patients with the frequent p.Ser263Pro mutation   [2008]

Milenković, Tatjana; Koehler, Katrin; Krumbholz, Manuela; Živanović, Slađana; Zdravković, Dragan S.; Huebner, Angela

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