Претрага
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;Voiding Cystourethrography - Do We Over-Do IT [2017]
Zivkovic, Dragana ; Sarac, Dragan; Fratric, IvanaChanges 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 SClinical 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, RadeHypertensive 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, EmilijaPredictive 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, Vesna4q34.1-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, MilenaGenotype 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, ZsuzsannaPrimary 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, NadaThree 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, AngelaФилтери
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