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Browsing by Author Kuburovic, Vladimir

Showing results 1 to 10 of 10
Issue DateTitleAuthor(s)TypeМp-cat.
2010An unusual presentation of cardiomyopathy in a patient with microcephaly-cardiomyopathy syndromeKuburovic, Vladimir; Vukomanovic, Vladislav A; Kosutic, Jovan Lj; Rakic, Sanja; Kuburovic, Nina BArticle
23M23
2011Assessment of health care quality in the tertiary level pediatric hospitals in SerbiaKuburovic, Nina; Djuricic, Slavisa; Neskovic, Andjelija; Dedić, Velimir  ; Kuburovic, VladimirArticle
23M23
2013Differences in the clinical spectrum of two adolescent male patients with Alstrom syndromeKuburovic, Vladimir; Marshall, Jan D; Collin, Gayle B; Nykamp, Keith; Kuburovic, Nina B; Milenkovic, Tatjana; Rakic, Sanja; Djuric, Milena Lj; Jecmenica, Jovana R; Milenkovic, Svetislav M;
Naggert, Juergen K;
Article
23M23
2012Liddle syndrome in a Serbian family and literature review of underlying mutationsBogdanovic, Radovan M; Kuburovic, Vladimir; Stajic, Natasa; Mughal, S; Hilger, A; Ninic, Sanja; Prijic, Sergej M  ; Ludwig, MichaelArticle
21M21
2011Liddle syndrome: the first family with proven mutation (PRO618SER) in the southeastern EuropeBogdanovic, Radovan M; Kuburovic, Vladimir; Stajic, Natasa; Mughal, S; Hilger, A; Kosutic, Jovan Lj; Ninic, Sanja; Prijic, Sergej M  ; Vukomanovic, Vladislav A; Ludwig, MichaelConference Paper
Mp. category will be shown later
2020Mowat-Wilson syndrome: growth chartsIvanovski, Ivan P ; Djuric, Olivera S; ...; Cuturilo, Goran; ...; Kuburovic, Vladimir; ...; (broj, koautora 53)Article
21M21
2020Mowat-Wilson syndrome: growth chartsIvanovski, I; ...; Cuturilo, Goran; ...; Kuburovic, Vladimir; ...; (broj, koautora 50)Conference Paper
Mp. category will be shown later
2018Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for careIvanovski, Ivan ; Đurić, Olivera ; Caraffi, Stefano Giuseppe; Santodirocco, Daniela; Pollazzon, Marzia; Rosato, Simonetta; Cordelli, Duccio Maria; Abdalla, Ebtesam; Accorsi, Patrizia; Adam, Margaret P.;
Ajmone, Paola Francesca; Badura-Stronka, Magdalena; Baldo, Chiara; Baldi, Maddalena; Bayat, Allan; Bigoni, Stefania; Bonvicini, Federico; Breckpot, Jeroen; Callewaert, Bert; Cocchi, Guido; Cuturilo, Goran; De, Brasi Daniele; Devriendt, Koenraad; Dinulos, Mary Beth; Hjortshøj, Tina Duelund; Epifanio, Roberta; Faravelli, Francesca; Fiumara, Agata; Formisano, Debora; Giordano, Lucio; Grasso, Marina; Grønborg, Sabine; Iodice, Alessandro; Iughetti, Lorenzo; Kuburovic, Vladimir; Kutkowska-Kazmierczak, Anna; Lacombe, Didier; Lo, Rizzo Caterina; Luchetti, Anna; Malbora, Baris; Mammi, Isabella; Mari, Francesca; Montorsi, Giulia; Moutton, Sebastien; Møller, Rikke S.; Muschke, Petra; Nielsen, Jens Erik Klint; Obersztyn, Ewa; Pantaleoni, Chiara; Pellicciari, Alessandro; Pisanti, Maria Antonietta; Prpic, Igor; Poch-Olive, Maria Luisa; Raviglione, Federico; Renieri, Alessandra; Ricci, Emilia; Rivieri, Francesca; Santen, Gijs W.; Savasta, Salvatore; Scarano, Gioacchino; Schanze, Ina; Selicorni, Angelo; Silengo, Margherita; Smigiel, Robert; Spaccini, Luigina; Sorge, Giovanni; Szczaluba, Krzysztof; Tarani, Luigi; Tone, Luis Gonzaga; Toutain, Annick; Trimouille, Aurelien; Te, Valera Elvis rci; Vergano, Samantha Schrier; Zanotta, Nicoletta; Zenker, Martin; Conidi, Andrea; Zollino, Marcella; Rauch, Anita; Zweier, Christiane; Garavelli, Livia;
Article
21a+M21a+
2012Recurrent Left Atrial Myxomas in Carney Complex: A Genetic Cause of Multiple Strokes that can be PreventedBriassoulis, George; Kuburovic, Vladimir; Xekouki, Paraskevi; Patronas, Nicholas; Keil, Meg F; Lyssikatos, Charalampos; Stajevic, Mila S  ; Kovacevic, Gordana S  ; Stratakis, Constantine AArticle
22M22
2011Two cases of LEOPARD syndrome-RAF1 mutations firstly described in childrenKuburovic, Vladimir; Vukomanovic, Vladislav A; Carcavilla, Atilano; Ezquieta-Zubicaray, Begona; Kuburovic, Nina BArticle
23M23