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Research outputs
Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease
[2024]
Damnjanović, Tatjana The JAK2 exon 12 mutations in V617F negative patients with erythrocytosis [2024]
Todoric-Zivanovic, Biljana; Strnad, Milica K; Atanaskovic, Lavinika; Elez, Marija NPredictors of low efficiency of WES in patients with epilepsy [2024]
Novoselova, Olga; Klestova, Valeria; Povolotskaya, Inna; Bikanov, RomanDelineation of the phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy - Alport syndrome and thin basement membrane nephropathy [2022]
Riedhammer, Korbinian Maria; Braunisch, Matthias C; Comic, Jasmina; Lungu, Adrian; Putnik, Jovana; Milosevski-Lomic, Gordana; Gessner, Michaela; Stajic, Natasa; Patzer, Ludwig; Emini, Nora;
Tasic, Velibor; Hoefele, Julia;
Recurrent congenital microcephaly: a case report
[2020]
Komnenić-Radovanović, Milica Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience [2023]
Riedhammer, Korbinian Maria; Comic, Jasmina; Tasic, Velibor; Putnik, Jovana; Abazi-Emini, Nora; Paripovic, Aleksandra; Stajic, Natasa; Meitinger, Thomas; Nushi-Stavileci, Valbona; Berutti, Riccardo;
Braunisch, Matthias C; Hoefele, Julia;
MTHFR gene polymorphism as stroke risk factor in young patients
[2004]
Damnjanović, Tatjana Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression
[2020]
Pešić, Milica Influence of eNOS gene haplotypes and iNOS rs2297518 gene variant on severe complications and mortality in surgical patients with secondary peritonitis
[2020]
Gulić, Milica Study of IL6 and TNF genes polymorphisms as a risk factor for the development of early neurological disorders and subsequent consequences in neonates
[2023]
Đuranović, Ana Filters
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