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Преглед према Аутор Tasic, Velibor
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| Година | Наслов | Аутор(и) | Тип резултата | Мп-кат. |
|---|---|---|---|---|
| 2012 | A Novel GH1 Mutation in a Family with Isolated Growth Hormone Deficiency Type II | Gucev, Zoran; Tasic, Velibor; Šaranac, Ljiljana  ; Stobbe, Heike; Kratzsch, Jürgen; Klammt, Jürgen; Pfäffle, Roland | Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 2022 | Delineation of the phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy - Alport syndrome and thin basement membrane nephropathy | 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;
| Conference Paper | Mp. category will be shown later |
| 2024 | Diversity of kidney care referral pathways in national child health systems of 48 European countries | Tasic, Velibor; ...; Stojanovic, Vesna D  ; ...; (broj, koautora 53) | Научни чланак | 21M21 - Водећи међународни часопис категорије M21 |
| 2024 | Exome Sequencing in a Cohort of Individuals with Microscopic Hematuria and Clinical Suspicion of Type-IV-Collagen-Related-Nephropathy | Bittmann, Marina; Riedhammer, Korbinian Maria; Stajic, Natasa; Lungu, Adrian; Tasic, Velibor; Abazi, Emini Nora; Braunisch, Matthias C; Nushi, Stavileci Valbona; Paripovic, Aleksandra; Putnik, Jovana;
Comic, Jasmina; Hoefele, Julia;
| Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2022 | Exome Sequencing in Individuals with Congenital Anomalies of the Kidney and Urinary Tract (Cakut): a Single-Center Experience | Comic, Jasmina; Riedhammer, Korbinian Maria; Tasic, Velibor; Putnik, Jovana; Abazi-Emini, Nora; Paripovic, Aleksandra; Stajic, Natasa; Nushi-Stavileci, Valbona; Braunisch, Matthias C; Hoefele, Julia | Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2023 | Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experience | 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;
| Научни чланак | 21M21 - Водећи међународни часопис категорије M21 |
| 2009 | Five Novel Mutations In Cystinuria Genes Slc3a1 And Slc7a9 | Popovska-Jankovic, Katerina; Tasic, Velibor; Bogdanovic, Radovan M; Miljkovic, Predrag; Baskin, E; Efremov, G; Plaseska-Karanfilska, Dijana | Научни чланак | 23M23 - Међународни часопис категорије M23 |
| 2022 | 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) | 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;
| Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2024 | Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4</i>? | 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;
| Научни чланак | 22M22 - Међународни часопис категорије M22 |
| 2018 | Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort | Zaniew, Marcin; Bökenkamp, Arend; Kołbuc, Marcin; La, Scola Claudio; Baronio, Federico; Niemirska, Anna; Szczepańska, Maria; Bürger, Julia; La Manna, Angela; Miklaszewska, Monika;
Rogowska-Kalisz, Anna; Gellermann, Jutta; Zampetoglou, Argyroula; Wasilewska, Anna; Roszak, Magdalena; Moczko, Jerzy; Krzemień, Aleksandra; Runowski, Dariusz; Siteń, Grzegorz; Załuska-Leśniewska, Iga; Fonduli, Patrizia; Zurrida, Franca; Paglialonga, Fabio; Gucev, Zoran; Paripović, Dušan
; Rus, Rina; Said-Conti, Valerie; Sartz, Lisa; Chung, Woo Yeong; Park, Se Jin; Lee, Jung Won; Park, Yong Hoon; Ahn, Yo Han; Sikora, Przemysław; Stefanidis, Constantinos J.; Tasic, Velibor; Konrad, Martin; Anglani, Franca; Addis, Maria; Cheong, Hae Il; Ludwig, Michael; Bockenhauer, Detlef; | Научни чланак | 21aM21a - Водећи међународни часопис категорије M21a |
| 2014 | Mild Recessive Mutations in Six Fraser Syndrome-Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract | 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;
| Научни чланак | 21a+M21a+ - Водећи међународни часопис категорије M21a+ |
| 2014 | Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract | 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;
| Научни чланак | 21a+M21a+ - Водећи међународни часопис категорије M21a+ |
| 2006 | Mutations in uroplakin IIIA are a rare cause of renal hypodysplasia in humans | Schonfelder, EM; Knuppel, T; Tasic, Velibor; Miljkovic, Predrag; Konrad, Martin; Wuhl, E; Antignac, C; Bakkaloglu, A; Schaefer, F; Weber, Stefanie | Научни чланак | 21aM21a - Водећи међународни часопис категорије M21a |
| 2024 | Phenotypic and genotypic spectrum of familial cases with congenital anomalies of the kidney and urinary tract (CAKUT) | Schniedermeier, Timo; Goldammer, Stephanie; Tasic, Velibor; Vollhardt, Anne; Abazi, Emini Nora; Gessner, Michaela; Putnik, Jovana; Stavileci, Valbona; Mueller, Dominik; Specht, Sabine;
Stajic, Natasa; Braunisch, Matthias C; Riedhammer, Korbinian Maria; Weber, Stefanie; Hoefele, Julia;
| Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2023 | Phenotypic Variability of Individuals with Cakut | Kraljevic, Bernard; Riedhammer, Korbinian M; Tasic, Velibor; Abazi-Emini, Nora; Gessner, Michaela; Lange-Sperandio, Baerbel; Stavileci, Valbona; Putnik, Jovana; Paripovic, Aleksandra; Stajic, Natasa;
Comic, Jasmina; Hoefele, Julia;
| Конференцијски рад | Мп категорија ће бити приказана накнадно. |
| 2019 | Treatment and long-term outcome in primary distal renal tubular acidosis | Lopez-Garcia, Sergio Camilo; Emma, Francesco; Walsh, Stephen B; Fila, Marc; Hooman, Nakysa; Zaniew, Marcin; Bertholet-Thomas, Aurélia; Colussi, Giacomo; Burgmaier, Kathrin; Levtchenko, Elena;
Sharma, Jyoti; Singhal, Jyoti; Soliman, Neveen A; Ariceta, Gema; Basu, Biswanath; Murer, Luisa; Tasic, Velibor; Tsygin, Alexey; Decramer, Stéphane; Gil-Peña, Helena; Koster-Kamphuis, Linda; La, Scola Claudio; Gellermann, Jutta; Konrad, Martin; Lilien, Marc; Francisco, Telma; Tramma, Despoina; Trnka, Peter; Yüksel, Selçuk; Caruso, Maria Rosa; Chromek, Milan; Ekinci, Zelal; Gambaro, Giovanni; Kari, Jameela A; König, Jens; Taroni, Francesca; Thumfart, Julia; Trepiccione, Francesco; Winding, Louise; Wühl, Elke; Ağbaş, Ayşe; Belkevich, Anna; Vargas-Poussou, Rosa; Blanchard, Anne; Conti, Giovanni; Boyer, Olivia; Dursun, Ismail; Pınarbaşı, Ayşe Seda; Melek, Engin; Miglinas, Marius; Novo, Robert; Mallett, Andrew; Milosevic, Danko; Szczepanska, Maria; Wente, Sarah; Cheong, Hae Il; Sinha, Rajiv; Gucev, Zoran; Dufek, Stephanie; Iancu, Daniela; Peco Antić, Amira
; Kaur, Amrit; Paglialunga, Antonino; Servais, Aude; Lutovac, Branko; Hoorn, Ewout J; Shasha-Lavsky, Hadas; Harambat, Jerome; Godron-Dubrasquet, Astrid; Buder, Kathrin; Allard, Lise; Patzer, Ludwig; Shumikhina, Marina; Hansen, Matthias; Printza, Nikoleta; Küçük, Nuran; Beringer, Ortraud; Bhimma, Rajendra; Cerkauskiene, Rimante; Neuhaus, Thomas J; Stavileci, Valbona; Ulinski, Tim; Dincel, Nida Temizkan; Mohebbi, Nilufar; Kleta, Robert; Schaefer, Franz; Bockenhauer, Detlef; | Научни чланак | 21aM21a - Водећи међународни часопис категорије M21a |
| 2014 | Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association | Saisawat, Pawaree; Kohl, Stefan; Hilger, Alina C; Hwang, Daw-Yang; Gee, Heon Yung; Dworschak, Gabriel C; Tasic, Velibor; Pennimpede, Tracie; Natarajan, Sivakumar; Sperry, Ethan;
Matassa, Danilo S; Stajic, Natasa; Bogdanovic, Radovan M; de, Blaauw Ivo; Marcelis, Carlo LM; Wijers, Charlotte HW; Bartels, Enrika; Schmiedeke, Eberhard; Schmidt, Dominik; Maerzheuser, Stefanie; Grasshoff-Derr, Sabine; Holland-Cunz, Stefan; Ludwig, Michael; Noethen, Markus M; Draaken, Markus; Brosens, Erwin; Heij, Hugo; Tibboel, Dick; Herrmann, Bernhard G; Solomon, Benjamin D; de, Klein Annelies; van, Rooij Iris ALM; Esposito, Franca; Reutter, Heiko M; Hildebrandt, Friedhelm;
| Научни чланак | 21a+M21a+ - Водећи међународни часопис категорије M21a+ |