Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Jovana Putnik"'
Autor:
Aleksandra Paripović, Nataša Stajić, Jovana Putnik, Slavica Ostojić, Biljana Alimpić, Adrijan Sarajlija
Publikováno v:
Global Pediatrics, Vol 8, Iss , Pp 100145- (2024)
This case report describes a patient harboring TARS2 mutations where chronic kidney disease stands out as the predominant clinical feature. The distinct manifestation observed in this case underscores the importance of continual exploration and docum
Externí odkaz:
https://doaj.org/article/a4005024dfab4a83a285e2e941d24677
Autor:
Jasmina Ćomić, Korbinian M. Riedhammer, Roman Günthner, Christian W. Schaaf, Patrick Richthammer, Hannes Simmendinger, Donald Kieffer, Riccardo Berutti, Velibor Tasic, Nora Abazi-Emini, Valbona Nushi-Stavileci, Jovana Putnik, Nataša Stajic, Adrian Lungu, Oliver Gross, Lutz Renders, Uwe Heemann, Matthias C. Braunisch, Thomas Meitinger, Julia Hoefele
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Disease-causing variants in COL4A3-5 are associated with type-IV-collagen-related nephropathy, a genetically and phenotypically multifaceted disorder comprising Alport syndrome (AS) and thin basement membrane nephropathy (TBMN) and autosomal, X-linke
Externí odkaz:
https://doaj.org/article/00d7a4d3a820481e94eec216b9d586ac
Autor:
Jaap W. Groothoff, Ella Metry, Lisa Deesker, Sander Garrelfs, Cecile Acquaviva, Reham Almardini, Bodo B. Beck, Olivia Boyer, Rimante Cerkauskiene, Pietro Manuel Ferraro, Luitzen A. Groen, Asheeta Gupta, Bertrand Knebelmann, Giorgia Mandrile, Shabbir S. Moochhala, Agnieszka Prytula, Jovana Putnik, Gill Rumsby, Neveen A. Soliman, Bhaskar Somani, Justine Bacchetta
Publikováno v:
Nature reviews. Nephrology, 19(3), 194-211. Nature Publishing Group
Nat Rev Nephrol
ISSN
Nat Rev Nephrol
ISSN
Primary hyperoxaluria (PH) is an inherited disorder that results from the overproduction of endogenous oxalate, leading to recurrent kidney stones, nephrocalcinosis and eventually kidney failure; the subsequent storage of oxalate can cause life-threa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5f447c83d0936f643cfc69826ac7d26
https://pure.amc.nl/en/publications/clinical-practice-recommendations-for-primary-hyperoxaluria(ab09f0b8-3434-4c08-918c-81ddf53300b3).html
https://pure.amc.nl/en/publications/clinical-practice-recommendations-for-primary-hyperoxaluria(ab09f0b8-3434-4c08-918c-81ddf53300b3).html
Autor:
Korbinian M. Riedhammer, Jasmina Ćomić, Velibor Tasic, Jovana Putnik, Nora Abazi-Emini, Aleksandra Paripovic, Natasa Stajic, Thomas Meitinger, Valbona Nushi-Stavileci, Riccardo Berutti, Matthias C. Braunisch, Julia Hoefele
Individuals with congenital anomalies of the kidney and urinary tract (CAKUT) show a broad spectrum of malformations. CAKUT can occur in an isolated fashion or as part of a syndromic disorder and can lead to end-stage kidney failure. A monogenic caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fe93b600d7c95a0780a7b6a7d115b3b
https://doi.org/10.21203/rs.3.rs-2251540/v1
https://doi.org/10.21203/rs.3.rs-2251540/v1
Publikováno v:
PRILOZI. 42:109-115
Introduction: Atypical hemolytic uremic syndrome (aHUS) is a rare form of thrombotic microangiopathy, caused by dysregulation of the complement alternative pathway. Deletion of the complement factor H–related genes, CFHR1 and CFHR3, together with t
Autor:
Aleksandra Paripović, Radovan Bogdanovic, Natasa Stajic, Vukomanović Vladislav, Jovana Putnik, Ana Gazikalović
Publikováno v:
Nephrologietherapeutique. 16(7)
Aim Aim of the study was to determine if carotid intima media thickness in children with idiopathic nephrotic syndrome is greater than in healthy subjects, and to assess whether carotid intima media thickness in children with nephrotic syndrome is as
Autor:
Barbara Uetz, Christoph Schmaderer, Lutz Renders, Carmen Montoya, Natasa Stajic, Marc Weidenbusch, Korbinian M. Riedhammer, Velibor Tasic, Matthias C. Braunisch, Matias Wagner, Julia Hoefele, Valbona Nushi-Stavileci, Jovana Putnik, Roman Günthner, Sabine Ponsel, Peter Strotmann, Baerbel Lange-Sperandio, Clara Hemmer, Zoran Gucev, Tim M. Strom
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 76(4)
Rationale & Objective Hereditary nephropathies are clinically and genetically heterogeneous disorders. For some patients, the clinical phenotype corresponds to a specific hereditary disease but genetic testing reveals that the expected genotype is no
Autor:
Rajit K Basu, Ahmad Kaddourah, Stuart L Goldstein, Ayse Akcan-Arikan, Megan Arnold, Cody Cruz, Michele Goldsworthy, Nancy Jaimon, Stephen Alexander, Marino Festa, Deirdre Hahn, Lauren Brown, Ari Jeon, Akash Deep, David Askenazi, Sean Bagshaw, Catherine Morgan, Rashid Alobaidi, Rajit Basu, David Cooper, Stuart Goldstein, Theresa Mottes, Tara Terrell, Patricia Arnold, Christina Metcalf, Shalayna Woodley, Radovan Bogdanović, Natasa Stajić, Branko Kovacevic, Amira Peco-Antic, Aleksandra Paripovic, Patrick Brophy, Timothy Bunchman, Duane Williams, Michelle Hoot, Vimal Chadha, Keefe Davis, Vikas Dharnidharka, Leslie Walther, Vincent Faustino, Janet Taft, Joana Tala, Katja Gist, Danielle Soranno, Il Soo Ha, Hee Gyung Kang, Richard Hackbarth, Mary Avendt-Reeber, Chloe Butler, Doug DeGraaf, Dawn Eding, Nathalie Hautala, Akunne Ndika, Eka Laksmi Hidayati, Songming Huang, Sean Kennedy, Madeleine Didsbury, Hari Kushartono, Risky Prasetyo, Cherry Mammen, Matthew Paden, Cheryl Stone, Stefano Picca, Federica Connola, James Schneider, Todd Sweberg, Aaron Kessel, David Selewski, Susan Hieber, Brankica Spasojević-Dimitrijeva, Ivana Ivanisevic, Jovana Putnik, Snezana Ristic, Scott Sutherland, Amy Staples, Craig Wong, Senan Hadid, Catherine Joseph, Robert Woroniecki, Michael Zappitelli, Noha Elsaerafy, Joshua Zaritsky
Summary Background Acute kidney injury occurs in one in four children admitted to an intensive care unit (ICU) and its severity is independently associated with increased patient morbidity and mortality. Early prediction of acute kidney injury has th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e36ecea4c07aa90e346f6ecbccb98957
https://europepmc.org/articles/PMC6053052/
https://europepmc.org/articles/PMC6053052/
Autor:
Radovan Bogdanovic, Natasa Stajic, Aleksandra Paripović, Jovana Putnik, Shinji Kunishima, Milos Kuzmanovic
Publikováno v:
Vojnosanitetski Pregled, Vol 71, Iss 4, Pp 395-398 (2014)
Vojnosanitetski pregled (2014) 71(4):395-398
Vojnosanitetski pregled (2014) 71(4):395-398
Introduction. The group of autosomal dominant disorders - Epstein syndrome, Sebastian syndrome, Fechthner syndrome and May-Hegglin anomaly - are characterised by thrombocytopenia with giant platelets, inclusion bodies in granulocytes and variable lev
Autor:
Aleksandra Paripović, Natasa Stajic, Gordana Basta-Jovanovic, Jovana Putnik, Radovan Bogdanovic
Publikováno v:
Modern Rheumatology. 23:182-189
Renal tubular acidosis (RTA) is common in adults with primary Sjogren syndrome (pSS) but to date this condition has only been identified in 12 pediatric cases of pSS. Here we present the case of a 13-year-old, otherwise asymptomatic girl in whom the