Pronađeno: 1-10 / 44 radova

Autori: Paripovic Aleksandra

>> Filter: Samo Article i Review

>> Sve godine

Naslov Exome Sequencing in a Cohort of Individuals with Microscopic Hematuria and Clinical Suspicion of Type-IV-Collagen-Related-Nephropathy (Meeting Abstract)
Autori 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 
Info PEDIATRIC NEPHROLOGY, (2024), vol. 39 br. 1, Suppl. S, str. S260-S260
Ispravka Web of Science   Elečas   Rang časopisa  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Global longitudinal strain (GLS) in children with idiopathic nephrotic syndrome (Meeting Abstract)
Autori Paripovic Aleksandra Stajic Natasa Putnik Jovana  Popovic Sasa S Krasic Stasa D  Vukomanovic Vladislav A 
Info PEDIATRIC NEPHROLOGY, (2024), vol. 39 br. 1, Suppl. S, str. S235-S235
Ispravka Web of Science   Elečas   Rang časopisa  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Acute kidney injury in suicide attempt due to overdose of bismuth subcitrate (Meeting Abstract)
Autori Putnik Jovana  Paripovic Aleksandra Stajic Natasa 
Info PEDIATRIC NEPHROLOGY, (2024), vol. 39 br. 1, Suppl. S, str. S127-S127
Ispravka Web of Science   Elečas   Rang časopisa  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Very early and severe presentation of Triple A syndrome - case report and review of the literature (Review)
Autori Cehic Maja  Mitrovic Katarina Vukovic Rade M  Milenkovic Tatjana Kovacevic Gordana S  Todorovic Sladjana  Panic-Zaric Sanja Cvetkovic Dimitrije Paripovic Aleksandra Huebner Angela Koehler Katrin Quitter Friederike 
Info FRONTIERS IN ENDOCRINOLOGY, (2024), vol. 15 br. , str. -
Projekat Else Kroner-Fresenius-Stiftung; Eva Luise und Horst Kohler-Stiftung; Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [314061271-TRR 205/2]
Ispravka Web of Science   Članak   Elečas   Rang časopisa  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity? (Article)
Autori Ilic Nikola A  Maric Nina ... Kravljanac Ruzica M Cirkovic Jana Krstic Jovana Radivojevic Danijela  Cirkovic Sanja S Ostojic Slavica B  Krasic Stasa D  Paripovic Aleksandra Vukomanovic Vladislav A ...  Maric Gorica D  Sarajlija Adrijan  
Info GENES, (2024), vol. 15 br. 6, str. -
Ispravka Web of Science   Članak   Elečas   Rang časopisa  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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  
Info BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64
Ispravka Web of Science   Članak   Elečas   Rang časopisa  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Complicated Urinary Tract Infection in Children (Meeting Abstract)
Autori Paripovic Aleksandra Putnik Jovana  Stajic Natasa 
Info PEDIATRIC NEPHROLOGY, (2023), vol. 38 br. , Suppl. 2, str. S152-S152
Ispravka Web of Science   Elečas   Rang časopisa  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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:
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
>> Sve godine

Ispis zapisa u formatu:TXT | BibTeX