Autori: Stajic Natasa
Naslov | Severe neurological complications in a child with multisystem inflammatory syndrome in children after asymptomatic COVID-19 (Article) |
Autori | Kravljanac Ruzica M Stajic Natasa Vukomanovic Vladislav A Petrovic Gordana Kuzmanovic Milos B |
Info | SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2024), vol. 152 br. 3-4, str. 182-185 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
Naslov | Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4? (Article; Early Access) |
Autori | Riedhammer Korbinian M 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. br. , str. - |
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 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; Early Access) |
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. br. , str. - |
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; Early Access) |
Autori | Trautmann Agnes ... Stajic Natasa ... (broj koautora 28) |
Info | PEDIATRIC NEPHROLOGY, (2022), vol. br. , str. - |
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 |