Autori: Tasic Velibor
Naslov | Diversity of kidney care referral pathways in national child health systems of 48 European countries (Article) |
Autori | Tasic Velibor ... Stojanovic Vesna D ... (broj koautora 53) |
Info | FRONTIERS IN PEDIATRICS, (2024), vol. 12 br. , str. - |
Ispravka | 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) |
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. 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: |
|
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 | Web of Science 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 | Web of Science Članak Elečas Rang časopisa Citati: |
|
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 | Web of Science Elečas Rang časopisa Citati: 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 | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
|
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 |
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 |
|
Naslov | Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract (Article) |
Autori | Kohl Stefan Hwang Daw-Yang Dworschak Gabriel C Hilger Alina C Saisawat Pawaree Vivante Asaf Stajic Natasa Bogdanovic Radovan M Reutter Heiko M Kehinde Elijah O Tasic Velibor Hildebrandt Friedhelm |
Info | JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2014), vol. 25 br. 9, str. 1917-1922 |
Projekat | National Institutes of Health [R01-DK045345, R01-DK088767] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
|
Naslov | Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract (Article) |
Autori | Hwang Daw-Yang Dworschak Gabriel C Kohl Stefan Saisawat Pawaree Vivante Asaf Hilger Alina C Reutter Heiko M Soliman Neveen A Bogdanovic Radovan M Kehinde Elijah O Tasic Velibor Hildebrandt Friedhelm |
Info | KIDNEY INTERNATIONAL, (2014), vol. 85 br. 6, str. 1429-1433 |
Projekat | National Institutes of Health [R01-DK088767]; March of Dimes Foundation [6FY11-241] |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
|