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 | 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 | The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy-A human genetics department experience (Article) |
Autori | Comic Jasmina ... Nushi-Stavileci Valbona Putnik Jovana Stajic Natasa ... (broj koautora 20) |
Info | FRONTIERS IN MEDICINE, (2022), vol. 9 br. , str. - |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract (Article) |
Autori | Zheng Bixia ... Stajic Natasa ... (broj koautora 17) |
Info | NEPHROLOGY DIALYSIS TRANSPLANTATION, (2022), vol. 37 br. 10, str. 1833-1843 |
Projekat | Begg Family Foundation; program of China Scholarships Council [201908320472]; Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [442070894]; Health Research Board, Ireland [HPF-206-674]; International Pediatric Research Foundation Early Investigators' Exchange Program; Irish Nephrology Society Specialist Registrar Bursary - Eugen Drewlo Chair for Kidney Research and Innovation at the Schulich School of Medicine & Dentistry at Western University, London, Ontario, Canada; American College of Medical Genetics and Genomics Foundation; National Institutes of Health [T32-DK007726, U54HG006504] |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy (Article) |
Autori | Garam Nora ... Stajic Natasa ... (broj koautora 68) |
Info | FRONTIERS IN IMMUNOLOGY, (2021), vol. 12 br. , str. - |
Projekat | Premium Postdoctoral Fellowship Program of the Hungarian Academy of Sciences [PPD2018-016/2018]; Higher Education Institutional Excellence Program of the Ministry of Human Capacities in Hungary within the framework of the molecular biology thematic progra |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |