Autori: Stajic Natasa
| 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
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| Info | VOJNOSANITETSKI PREGLED, (2023), vol. 80 br. 3, str. 270-274 |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| 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
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| 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 | Web of Science Članak Elečas Rang časopisa Citati: |
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| 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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| 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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| 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
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| Info | PEDIATRIC NEPHROLOGY, (2022), vol. 37 br. 11, str. 2889-2889 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| 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
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| Info | PEDIATRIC NEPHROLOGY, (2022), vol. 37 br. 11, str. 2854-2854 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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| 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)
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| Info | FRONTIERS IN MEDICINE, (2022), vol. 9 br. , str. - |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | The first case of pediatric Cushing disease in Serbia (Meeting Abstract) |
| Autori | Panic-Zaric Sanja Vukovic Rade M Milenkovic Tatjana Mitrovic Katarina Todorovic Sladjana Ristic Snezana Stajic Natasa Putnik Jovana Paripovic Aleksandra Vukomanovic Vladislav A Ninic Sanja S Prijic Sergej M Popovic Sasa S Cerovic Ivana B Kitic Ivana Pasic Srdjan S Minic Predrag B Rodic Milan Kuzmanovic Milos B Jovic Milena Djordjevic-Milosevic Maja Pekic-Djurdjevic Sandra R Petakov Milan S Milicevic Mihailo Jovanovic Milan D
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| Info | HORMONE RESEARCH IN PAEDIATRICS, (2022), vol. 95 br. SUPPL 2, Suppl. 2, str. 444-444 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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| 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 | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Delineation of the phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy - Alport syndrome and thin basement membrane nephropathy (Meeting Abstract) |
| Autori | 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
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| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2022), vol. 30 br. SUPPL 1, Suppl. 1, str. 141-142 |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science |
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