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Autori: Tasic Velibor

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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  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati:
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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)
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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  
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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  
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Naslov Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association (Article)
Autori 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 
Info KIDNEY INTERNATIONAL, (2014), vol. 85 br. 6, str. 1310-1317
Projekat National Institutes of Health [R01-DK045345, R01-DK088767]; March of Dimes Foundation [6FY11-241]; Division of Intramural Research; National Human Genome Research Institute (NHGRI); National Institutes of Health and Human services; Bundesministerium fur B
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Molecular characterization of cystinuria in south-eastern European countries (Article)
Autori Popovska-Jankovic Katerina Tasic Velibor Bogdanovic Radovan M Miljkovic Predrag Golubovic Emilija  Soylu A Saraga Marjan Pavicevic Snezana Baskin E Akil I Gregoric Alojz Lilova Marusia Topaloglu R Sukarova-Stefanovska Emilija Plaseska-Karanfilska D 
Info UROLITHIASIS, (2013), vol. 41 br. 1, str. 21-30
Projekat Science Funds of the Research Centre for Genetic Engineering and Biotechnology (RCGEB)
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov A Novel GH1 Mutation in a Family with Isolated Growth Hormone Deficiency Type II (Article)
Autori Gucev Zoran Tasic Velibor Saranac Ljiljana Stobbe Heike Kratzsch Juergen Klammt Juergen Pfaeffle Roland 
Info HORMONE RESEARCH IN PAEDIATRICS, (2012), vol. 77 br. 3, str. 1-5
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Five Novel Mutations In Cystinuria Genes Slc3a1 And Slc7a9 (Article)
Autori Popovska-Jankovic Katerina Tasic Velibor Bogdanovic Radovan M Miljkovic Predrag Baskin E Efremov G Plaseska-Karanfilska Dijana 
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2009), vol. 12 br. 1, str. 15-20
Projekat Macedonian Academy of Sciences and Arts, Skopje, Republic of Macedonia [09-59/1]
Ispravka Web of Science   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov CLDN16 genotype predicts renal decline in familial hypomagnesemia with hypercalciuria and nephrocalcinosis (Article)
Autori Konrad Martin Hou Jianghui Weber Stefanie Doetsch Joerg Kari Jameela A Seeman Tomas Kuwertz-Broeking Eberhard Peco-Antic Amira E Tasic Velibor Dittrich Katalin Alshaya Hammad O von Vigier Rodo O Gallati Sabina Goodenough Daniel A Schaller Andre 
Info JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, (2008), vol. 19 br. 1 , Suppl. , str. 171 -181
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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