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Research outputs

Immunization Coverage and the Reasons for Unvaccination in Indjija, Srem District, Republic of Serbia   [2019]

Petrovic, Vesna; Visnjevac, Danilo; Rozek-Mitrovic, Tanja

Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature   [2000]

Boerkoel, Cornelius F; O'Neill, S; Andre, Jean-Luc; Benke, PJ; Bogdanovic, Radovan M; Bulla, M; Burguet, A; Cockfield, Sandra; Cordeiro, Isabel; Ehrich, Jochen HH;
Frund, S; Geary, DF; Ieshima, A; Illies, F; Joseph, MW; Kaitila, I; Lama, Guiliana; Leheup, B; Ludman, MD; McLeod, DR; Medeira, A; Milford, David V; Ormala, T; Rener-Primec, Z; Santava, A; Santos, HG; Schmidt, Beate; Smith, Graham C; Spranger, J; Zupancic, N; Weksberg, R;

Liddle syndrome in a Serbian family and literature review of underlying mutations   [2012]

Bogdanovic, Radovan M; Kuburovic, Vladimir; Stajic, Natasa; Mughal, S; Hilger, A; Ninic, Sanja; Prijic, Sergej M  ; Ludwig, Michael

Microbiological aspects of vulvovaginitis in prepubertal girls (✓)   [2012]

Ranđelović, Gordana ; Mladenović, Vesna; Ristić, Ljiljana; Otašević, Suzana  ; Branković, Sofija; Mladenović-Antić, Snežana; Bogdanović, Milena; Bogdanović, Dragan  

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

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

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  

Pathogens causing urinary tract infections in infants: a European overview by the ESCAPE study group   [2015]

Alberici, Irene; ...; Peco-Antic, Amira E; ...; (broj, koautora 22)

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

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