Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Margareta Fistrek Prlić"'
Autor:
Ines Bosnić Kovačić, Matija Matošević, Mario Laganović, Živka Dika, Margareta Fištrek Prlić, Ema Ivandić, Marijana Ćorić, Stela Bulimbašić, Nadira Duraković, Zinaida Perić, Lana Desnica, Radovan Vrhovac, Bojan Jelaković, Sanjeev Sethi, Ivana Vuković Brinar
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-10 (2024)
Abstract Background Nephrotic syndrome (NS) is a rare complication that can occur after haematopoietic stem cell transplantation (HSCT). In patients with membranous nephropathy (MN) who have undergone allogeneic HSCT, a new antigen called protocadher
Externí odkaz:
https://doaj.org/article/93f1f8e038be4da48040a78691f73d24
Autor:
Nada Božina, Lana Ganoci, Livija Simičević, Katarina Gvozdanović, Iva Klarica Domjanović, Margareta Fistrek Prlić, Tena Križ, Ana Borić Bilušić, Mario Laganović, Tamara Božina
Publikováno v:
Arhiv za higijenu rada i toksikologiju
Volume 72
Issue 2
Volume 72
Issue 2
Statini i nesteroidni protuupalni lijekovi (NSAID) učestalo se propisuju, pa i kao konkomitantna terapija. Postoji značajna interindividualna razlika u osjetljivosti na njihove najčešće nuspojave. Rizični čimbenici za razvoj nuspojava tih lije
Autor:
Margareta Fistrek Prlic, Ivana Vukovic Brinar, Jelena Kos, Zivka Dika, Ema Ivandic, Mirjana Fucek, Bojan Jelakovic
Publikováno v:
Biomedicines, Vol 12, Iss 10, p 2233 (2024)
Background/Objectives: Hepatocyte growth factor (HGF) is a protective factor against acute renal injury and chronic renal fibrosis. A positive correlation between HGF and blood pressure (BP) has been established. This study aimed to determine the ass
Externí odkaz:
https://doaj.org/article/46e9d4fed651476095970449ff56aee9
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Externí odkaz:
https://doaj.org/article/aac11d66a76b48eeb6c49c7ade90242d
Autor:
Iva Sorić Hosman, Andrea Cvitković Roić, Margareta Fištrek Prlić, Ivana Vuković Brinar, Lovro Lamot
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Autosomal dominant polycystic kidney disease (ADPKD) is one of the leading causes of end-stage renal disease. In spite of the recent tremendous progress in the understanding of ADPKD pathogenesis, the molecular mechanisms of the disease remain incomp
Externí odkaz:
https://doaj.org/article/362f25a763bf43f6b6953d2ab36e6336
Autor:
Margareta Fistrek Prlic, Sanda Huljev Frkovic, Bodo Beck, Ivana Tonkovic Durisevic, Stela Bulimbasic, Marijana Coric, Lovro Lamot, Ema Ivandic, Ivana Vukovic Brinar
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionGenetic kidney diseases are underdiagnosed; namely, from 7% to 40% of patients suffering from chronic kidney disease (CKD) can carry a pathogenic variant, depending on population characteristics. Hereditary tubulointerstitial kidney disea
Externí odkaz:
https://doaj.org/article/87de7d133de64c65a9214404dda0a93a
Autor:
Sara Grlić, Viktorija Gregurović, Mislav Martinić, Maša Davidović, Ivanka Kos, Slobodan Galić, Margareta Fištrek Prlić, Ivana Vuković Brinar, Kristina Vrljičak, Lovro Lamot
Publikováno v:
Children, Vol 11, Iss 4, p 392 (2024)
Introduction: Pediatric cystic kidney disease (CyKD) includes conditions characterized by renal cysts. Despite extensive research in this field, there are no reliable genetics or other biomarkers to estimate the phenotypic consequences. Therefore, Cy
Externí odkaz:
https://doaj.org/article/4e16f1e0e252448699303e112be18f2d
Autor:
Margareta Fistrek Prlic, Marijana Coric, Laura Calabresi, Chiara Pavanello, Lorena Mosca, Ugo Cavallari, Ivana Vukovic Brinar, Sandra Karanovic, Mario Laganovic, Bojan Jelakovic
Publikováno v:
Atherosclerosis Plus, Vol 49, Iss , Pp 28-31 (2022)
Background and aims: We report the first two cases of familial lecithin:cholesterol acyltransferase (LCAT) deficiency in Croatia with classical clinical and biochemical features. Patients and methods: A 30-year-old man with nephrotic syndrome, cornea
Externí odkaz:
https://doaj.org/article/0af6f28a1d114651aac3088ffc570ee5
Autor:
Margareta Fistrek Prlic, Mislav Jelakovic, Marko Brinar, Dora Grgic, Ivan Romic, Zlatko Marusic, Ema Ivandic, Bojan Jelakovic, Ivana Vukovic Brinar, Zeljko Krznaric
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Chronic kidney disease (CKD) is a very common chronic non-communicable disease. Phosphate and calcium metabolism disorders are one of the most common features of CKD. Sevelamer carbonate is the most widely used non-calcium phosphate binder. Gastroint
Externí odkaz:
https://doaj.org/article/e27b64eb2af047b68f9e9630af672a4c
Autor:
Ema Ivandic, Marjan Maric, Vesna Elvedi-Gasparovic, Margareta Fistrek Prlic, Lovro Lamot, Bojan Jelakovic, Ivana Vukovic Brinar
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Cystinuria is a rare genetic disorder inherited by an autosomal recessive pattern which affects the transmembrane transporter for the base amino acid cystine. It has a general prevalence of 1 in 7000 with demographic variations. Patients with cystinu
Externí odkaz:
https://doaj.org/article/06f5c166e86348c8b463751b6cbc36ec