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Naslov Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4? (Article)
Autori Riedhammer Korbinian Maria  Simmendinger Hannes  Tasic Velibor  Putnik Jovana  Abazi-Emini Nora  Stajic Natasa  Berutti Riccardo  Weidenbusch Marc  Patzer Ludwig  Lungu Adrian  Milosevski-Lomic Gordana  Guenthner Roman  Braunisch Matthias C  Comic Jasmina  Hoefele Julia 
Info CLINICAL GENETICS, (2024), vol. 105 br. 4, str. 406-414
Projekat Deutsche Forschungsgemeinschaft; German Research Foundation (DFG); Technical University of Munich (TUM)
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21 (Article)
Autori Paripovic Aleksandra  Maver Ales  Stajic Natasa  Putnik Jovana  Ostojic Slavica B  Alimpic Biljana  Ilic Nina  Sarajlija Adrijan 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Complicated Urinary Tract Infection in Children (Meeting Abstract)
Autori Paripovic Aleksandra  Putnik Jovana  Stajic Natasa 
Info PEDIATRIC NEPHROLOGY, (2023), vol. 38 br. , Suppl. 2, str. S152-S152
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Phenotypic Variability of Individuals with Cakut (Meeting Abstract)
Autori Kraljevic Bernard  Riedhammer Korbinian Maria  Tasic Velibor  Abazi-Emini Nora  Gessner Michaela  Lange-Sperandio Baerbel  Stavileci Valbona  Putnik Jovana  Paripovic Aleksandra  Stajic Natasa  Comic Jasmina  Hoefele Julia 
Info PEDIATRIC NEPHROLOGY, (2023), vol. 38 br. , Suppl. 2, str. S54-S55
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Moyamoya syndrome in Schimke immuno-osseous dysplasia (Article)
Autori Vujic Ana J  Obradovic Slobodan  Igrutinovic Zoran R  Protrka Zoran M  Jankovic Marijana  Radovanovic Marija D  Stajic Natasa  Medovic Rasa H  Jankovic Sveta 
Info VOJNOSANITETSKI PREGLED, (2023), vol. 80 br. 3, str. 270-274
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience (Article)
Autori 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 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. 6, str. 674-680
Projekat CAKUT/UTI/Bladder Dysfunction of the European Society for Paediatric Nephrology (ESPN); German Research Foundation (DFG); Technical University of Munich (TUM)
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Outcomes of steroid-resistant nephrotic syndrome in children not treated with intensified immunosuppression (Article)
Autori Trautmann Agnes  ...  Stajic Natasa  ...  (broj koautora 28) 
Info PEDIATRIC NEPHROLOGY, (2023), vol. 38 br. 5, str. 1499-1511
Projekat Projekt DEAL; ERKNet, the European Rare Kidney Disease Reference Network; European Union
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract (Article)
Autori Wu Chen-Han Wilfred  ...  Stajic Natasa  ...  (broj koautora 36) 
Info EUROPEAN UROLOGY OPEN SCIENCE, (2022), vol. 44 br. , str. 106-112
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
Naslov Exome Sequencing in Individuals with Congenital Anomalies of the Kidney and Urinary Tract (Cakut): a Single-Center Experience (Meeting Abstract)
Autori Comic Jasmina  Riedhammer Korbinian Maria  Tasic Velibor  Putnik Jovana  Abazi-Emini Nora  Paripovic Aleksandra  Stajic Natasa  Nushi-Stavileci Valbona  Braunisch Matthias C  Hoefele Julia 
Info PEDIATRIC NEPHROLOGY, (2022), vol. 37 br. 11, str. 2889-2889
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science  
Naslov Genotype-Phenotype Correlation in a Cohort of Individuals with Disease-Causing Variants in COL4A3/COL4A4 Associated with Type-Iv-Collagen-Related Nephropathy (Alport Syndrome and Thin Basement Membrane Nephropathy) (Meeting Abstract)
Autori Simmendinger Hannes  Riedhammer Korbinian Maria  Tasic Velibor  Putnik Jovana  Abazi-Emini Nora  Stajic Natasa  Weidenbusch Marc  Patzer Ludwig  Lungu Adrian  Milosevski-Lomic Gordana  Braunisch Matthias C  Guenthner Roman  Comic Jasmina  Hoefele Julia 
Info PEDIATRIC NEPHROLOGY, (2022), vol. 37 br. 11, str. 2854-2854
Ispravka ISI/Web of Science   Elečas   Rang časopisa   Citati: ISI/Web of Science   Scopus  
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