Претрага
Резултати
Genotype phenotype correlation in a pediatric population with antithrombin deficiency
[2019]
Kovač, Mirjana 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, 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, Angela4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome [2011]
Čuturilo, GoranSocial-economic factors and irrational antibiotic use as reasons for antibiotic resistance of bacteria causing common childhood infections in primary healthcare [2011]
Ilić, Katarina; Jakovljević, Emil; Škodrić Trifunović, VesnaPathogens causing urinary tract infections in infants: a European overview by the ESCAPE study group [2015]
Alberici, Irene; ...; Peco-Antic, Amira E; ...; (broj, koautora 22)Triple A syndrome: 32 years experience of a single centre (1977-2008) [2010]
Milenkovic, Tatjana; Zdravkovic, Dragan S; Savic, Natasa; Todorovic, Sladjana; Mitrovic, Katarina; Koehler, Katrin; Huebner, AngelaClinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome [2009]
Toromanovic, Alma; Tahirovic, Husref; Milenkovic, Tatjana; Koehler, Katrin; Kind, Barbara; Zdravkovic, Dragan S; Hasanhodzic, Mensuda; Huebner, AngelaClinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia
[2021]
Raičević, Maja; Milenković, Tatjana; Hussain, Khalid; Đorđević, Maja Predictive genetic markers of coagulation, inflammation and apoptosis in Perthes disease - Serbian experience
[2015]
Srzentić, Sanja Филтери
По типу
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