Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Natasa Stajić"'
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:
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:
Chen-Han Wilfred Wu, Tze Y. Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Luca Schierbaum, Sophia Schneider, Nina Mann, Dervla M. Connaughton, Makiko Nakayama, Amelie T. van der Ven, Rufeng Dai, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Natasa Stajic, Neveen A. Soliman, Jameela A. Kari, Sherif El Desoky, Hanan M. Fathy, Danko Milosevic, Daniel Turudic, Muna Al Saffar, Hazem S. Awad, Loai A. Eid, Aravind Ramanathan, Prabha Senguttuvan, Shrikant M. Mane, Richard S. Lee, Stuart B. Bauer, Weining Lu, Alina C. Hilger, Velibor Tasic, Shirlee Shril, Simone Sanna-Cherchi, Friedhelm Hildebrandt
Publikováno v:
European Urology Open Science, Vol 44, Iss , Pp 106-112 (2022)
Background: Congenital anomalies of the kidneys and urinary tract (CAKUT) are the most common cause of chronic kidney disease among children and adults younger than 30 yr. In our previous study, whole-exome sequencing (WES) identified a known monogen
Externí odkaz:
https://doaj.org/article/3efb0bd1ab7841249ffc6b6938766552
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 139, Iss 1-2, Pp 37-43 (2011)
Introduction. Infants with urinary tract malformations (UTM) presenting with urinary tract infection (UTI) are prone to develop transient type 1 pseudohypoaldosteronism (THPA1). Objective. Report on patient series with characteristics of THPA1, UTM a
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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:
Aleksandar, Sovtić, Predrag, Minić, Radovan, Bogdanović, Natasa, Stajić, Milan, Rodić, Gordana, Marković-Sovtić
Publikováno v:
Vojnosanitetski pregled. 69(4)
Infants with cystic fibrosis may fail to thrive despite recommended caloric intake because of electrolyte disurbances caused by salt depletion resulting in hypochloremic metabolic alkalosis or pseudo-Bartter's syndrome. In most patients reported symp
Autor:
Radovan, Bogdanović, Vesna, Nikolić, Milos, Ognjanović, Jovan, Dimitrijević, Jasmina, Marković-Lipkovski, Srdjan, Pasić, Aleksandra, Minić, Natasa, Stajić
Publikováno v:
Srpski arhiv za celokupno lekarstvo. 130
In 53 children and adolescents (47 males, 6 females) with lupus nephritis, clinical features at the time of renal biopsy were analyzed and correlated with pathohistological findings. The mean age at the time of diagnosis of systemic lupus was 12.9 +/
Autor:
Radovan, Bogdanović, Vesna, Nikolić, Milos, Ognjanović, Jovan, Dimitrijević, Jasmina, Marković-Lipkovski, Srdjan, Pasić, Aleksandra, Minić, Natasa, Stajić
Publikováno v:
Srpski arhiv za celokupno lekarstvo. 130
In 53 children and adolescents (47 males, 6 females) with lupus nephritis, clinical features at the time of renal biopsy were analyzed and correlated with pathohistological findings. Therapeutic regimens used and the renal status at the end of follow
Autor:
Radovan, Bogdanović, Milos, Kuzmanović, Jasmina, Marković-Lipkovski, Milos, Ognjanović, Dragan, Mićić, Ivica, Stanković, Natasa, Stajić, Vesna, Nikolić, Gordana, Bunjevacki
Publikováno v:
Srpski arhiv za celokupno lekarstvo. 130(9-10)
Several reports have documented various forms of glomerular diseases in adults with myelodysplastic syndromes (MDS), but similar reports in children are lacking. We describe two children with MDS-associated with steroid-responsive nephrotic syndrome