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Research outputs

A randomized, controlled double-blind study comparing the efficacy and safety of dose-ranging voclosporin with placebo in achieving remission in patients with active lupus nephritis [2019]

Rovin, Brad H. ; Solomons, Neil; Pendergraft, William F.; ...; Jelačić, Rosa; Jovanović, Dragan; Mitić, Branka ; Peković, Gordana; Radović, Milan ; Radunović, Goran ;

...; (broj autora 103);

Mechanisms of vascular dysfunction in the interleukin-10-deficient murine model of preeclampsia indicate nitric oxide dysregulation [2021]

Cubro, Hajrunisa; ...; Milic, Natasa M; ...; Garovic, Vesna D

Has the time come for new diagnostic criteria of Balkan endemic nephropathy? [2004]

Radovic, Milan M ; Djukanovic, Ljubica D

Genetic screening in adolescents with steroid-resistant nephrotic syndrome [2013]

Lipska, Beata S; ...; Bogdanovic, Radovan M; ...; Peco-Antic, Amira E; ...; (broj, koautora 51)

Anti-nephrin autoantibodies in steroid-resistant nephrotic syndrome may inform treatment strategy [2025]

Hengel, Felicitas E.; Dehde, Silke; Yilmaz, Alev; Bayazit, Aysun K.; Ozaltin, Fatih; Paripović, Dušan ; Emma, Francesco; Ronco, Pierre; Vivarelli, Marina; Hogan, Julien;

Schaefer, Franz; Tomas, Nicola M.; Huber, Tobias B.;

Personalized dynamic risk assessment in nephrology is a next step in prognostic research [2018]

Brankovic, Milos; Kardys, Isabella; Hoorn, Ewout J; Baart, Sara; Eric, Boersma; Rizopoulos, Dimitris

Comments on ‘In patients with type 1 diabetes and new-onset microalbuminuria the development of advanced chronic kidney disease may not require progression to proteinuria’ [2010]

Mitrovic, Jelena S.; Ležaić, Višnja

Insights from ADPedKD, ERKReg and RaDaR registries provide a multi-national perspective on the presentation of childhood autosomal dominant polycystic kidney disease in high-and middle-income countries [2025]

Gimpel, Charlotte; ...; Paripović, Aleksandra; Paripović, Dušan ; ...; Spasojević, Brankica B. ; ...; (broj koautora 72)

Genotype-phenotype associations in WT1 glomerulopathy [2014]

Lipska, Beata S; ...; Peco-Antic, Amira E; ...; Bogdanovic, Radovan M; ...; (broj, koautora 27)

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association [2014]

Saisawat, Pawaree; Kohl, Stefan; Hilger, Alina C; Hwang, Daw-Yang; Gee, Heon Yung; Dworschak, Gabriel C; Tasic, Velibor; Pennimpede, Tracie; Natarajan, Sivakumar; Sperry, Ethan;

Matassa, Danilo S; Stajic, Natasa; Bogdanovic, Radovan M; de, Blaauw Ivo; Marcelis, Carlo LM; Wijers, Charlotte HW; Bartels, Enrika; Schmiedeke, Eberhard; Schmidt, Dominik; Maerzheuser, Stefanie; Grasshoff-Derr, Sabine; Holland-Cunz, Stefan; Ludwig, Michael; Noethen, Markus M; Draaken, Markus; Brosens, Erwin; Heij, Hugo; Tibboel, Dick; Herrmann, Bernhard G; Solomon, Benjamin D; de, Klein Annelies; van, Rooij Iris ALM; Esposito, Franca; Reutter, Heiko M; Hildebrandt, Friedhelm;