Autori: Stajic Natasa
| Naslov | COL4A5-p.Gly624Asp is the Predominant Variant in Europe Associated With a Mild Alport Syndrome Phenotype (Article) |
| Autori | Krueger Bastian M ... Putnik Jovana  Stajic Natasa ... (broj koautora 28)
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| Info | KIDNEY INTERNATIONAL REPORTS, (2025), vol. 10 br. 5, str. 1372-1383 |
| Projekat | German Research Foundation (DFG); Technical University of Munich (TUM); German Research Foundation (DFG) [HA 6908/4-1, HA 6908/7-1, HA 6908/8-1, HO 2583/13-1, RI 3503/3-1]; European Society for Pediatric Nephrology (ESPN) [2.2020] |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| 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 | Web of Science Članak Elečas Rang časopisa |
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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
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| Info | CLINICAL GENETICS, (2024), vol. 105 br. 4, str. 406-414 |
| Projekat | Deutsche Forschungsgemeinschaft; German Research Foundation (DFG); Technical University of Munich (TUM) |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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| 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
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| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64 |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| 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 | 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 | 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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