Search Results - "Galešić Ljubanović, Danica"

The 2019 and 2021 International Workshops on Alport Syndrome by Daga, Sergio, Ding, Jie, Deltas, Constantinos, Savige, Judy, Lipska-Ziętkiewicz, Beata S, Hoefele, Julia, Flinter, Frances, Gale, Daniel P, Aksenova, Marina, Kai, Hirofumi, Perin, Laura, Barua, Moumita, Torra, Roser, Miner, Jeff H, Massella, Laura, Ljubanović, Danica Galešić, Lennon, Rachel, Weinstock, Andrè B, Knebelmann, Bertrand, Cerkauskaite, Agne, Gear, Susie, Gross, Oliver, Turner, A Neil, Baldassarri, Margherita, Pinto, Anna Maria, Renieri, Alessandra

“…In 1927 Arthur Cecil Alport, a South African physician, described a British family with an inherited form of kidney disease that affected males more severely…”
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Immune-mediated diseases after coronavirus disease 2019 vaccination: rare but important complication by Zagorec, Nikola, Horvatic, Ivica, Senjug, Petar, Horacek, Matija, Ljubanovic, Danica Galesic, Galesic, Kresimir

“…Since the beginning of mass vaccination against coronavirus disease 2019 (COVID-19), vaccine-linked immune-mediated diseases have been increasingly reported…”
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PULMONARY HEMORRHAGE AND CRESCENTIC GLOMERULONEPHRITIS IN A PATIENT WITH SEROPOSITIVE ANTI-GLOMERULAR BASEMENT MEMBRANE DISEASE AND ANTI-NEUTROPHIL CYTOPLASMIC ANTIBODIES by Bernadette Sreter, Katherina, Pavlović, Draško, Tomić, Monika, Šenjug, Petar, Galešić Ljubanović, Danica

“…Anti-glomerular basement membrane (anti-GBM) disease is an acute and life-threatening systemic autoimmune disorder. The coexistence of circulating…”
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C4d Is an Independent Predictor of the Kidney Failure in Primary IgA Nephropathy by Zagorec, Nikola, Horvatić, Ivica, Kasumović, Dino, Osmani, Besa, Sović, Slavica, Nikić, Jagoda, Horaček, Matija, Šenjug, Petar, Galešić, Krešimir, Galešić Ljubanović, Danica

“…C4d deposits are present in a substantial proportion of patients with IgA nephropathy (IgAN), indicating the activation of the lectin pathway (LP) of the…”
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Letter to the Editor: Characterization of Choriocapillaris and Choroidal Abnormalities in Alport Syndrome by Bosnar, Damir, Knežic Zagorec, Mira, Bušic, Mladen, Cigic, Valentina, Zagorec, Nikola, Nikuševa Martic, Tamara, Galešic Ljubanovic, Danica

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Clinical and histopathological characteristics of COL4A3 c.2881+1G>A variant causing Alport spectrum disorders in Croatian population by Horaček, Matija, Nikuševa Martić, Tamara, Šenjug, Petar, Šenjug Perica, Marija, Oroz, Maja, Kuzmac, Sania, Klarić, Dragan, Glavina Durdov, Merica, Saraga, Marijan, Milošević, Danko, Batinić, Danica, Ćorić, Marijana, Paić, Frane, Galešić Ljubanović, Danica

“…Alport syndrome (AS) and thin basement membrane nephropathy (TBMN) are part of the spectrum of kidney disorders caused by pathogenic variants in α3, α4, or α5…”
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TIOPRONIN AND/OR NSAID? A CASE OF NEPHROTIC SYNDROME AND ACUTE INTERSTITIAL NEPHRITIS IN A YOUNG WOMAN WITH CYSTINURIA by Vidovic, Luka, Josipovic, Josipa, Senjug, Petar, Ljubanovic, Danica Galesic

“…Cystinuria is an autosomal recessive disease that leads to recurrent stone formation. Tiopronin, a glycine derivative with a free thiol similar to…”
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Clinical and pathohistological characteristics of Alport spectrum disorder caused by COL4A4 mutation c.193-2A>C: a case series by Šenjug, Petar, Nikuševa Martić, Tamara, Šenjug Perica, Marija, Oroz, Maja, Horaček, Matija, Gotovac Jerčić, Kristina, Galešić, Krešimir, Galešić Ljubanović, Danica

“…To present the pathohistological and clinical characteristics of five Croatian families with Alport spectrum disorders caused by splice acceptor pathogenic…”
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Resistant and Relapsing Collapsing Glomerulopathy Successfully Treated with Rituximab—A Case Report by Zagorec, Nikola, Klarić, Dragan, Klarić, Marta, Horvatić, Ivica, Šenjug, Petar, Horaček, Matija, Nikić, Jagoda, Galešić Ljubanović, Danica, Galešić, Krešimir

“…Collapsing glomerulopathy (CG) or collapsing focal segmental glomerulosclerosis (cFSGS) is an aggressive disease with a high tendency of progression to…”
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A Child with Dense Deposit Disease and Decreased Classic Complement Pathway Activity by Trutin, Ivana, Oletic, Lea, Ljubanovic, Danica Galesic, Turudic, Daniel, Milosevic, Danko

“…We report a rare case of nephritic syndrome underlying dense deposit disease (DDD) with alternative complement pathway dysfunction explained with both C3…”
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IgM as a novel predictor of disease progression in secondary focal segmental glomerulosclerosis by Pačić, Arijana, Šenjug, Petar, Bacalja, Jasna, Tišljar, Miroslav, Horvatić, Ivica, Bulimbašić, Stela, Knotek, Mladen, Galešić, Krešimir, Galešić Ljubanović, Danica

“…To determine the role of immunoglobulin M (IgM) deposits in clinical manifestations, disease outcome, and treatment response of idiopathic and secondary focal…”
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Epidemiology of 10-year paediatric renal biopsies in the region of southern Croatia by Arapović, Adela, Vukojević, Katarina, Filipović, Natalija, Glavina Durdov, Merica, Ljubanović-Galešić, Danica, Saraga-Babić, Mirna, Prgomet, Sandra, Simičić Majce, Ana, Belavić, Anja, Borić Škaro, Dijana, Ljutić, Dragan, Saraga, Marijan

“…Information about renal diseases in children is available from national registries of renal biopsies. Aim of the study was to compare the clinical presentation…”
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Autosomal recessive Alport syndrome caused by a novel COL4A4 splice site mutation: a case report by Šenjug, Petar, Nikuševa Martić, Tamara, Šenjug Perica, Marija, Oroz, Maja, Horaček, Matija, Ćuk, Martin, Abdović, Slaven, Galešić Ljubanović, Danica

“…Alport syndrome (AS) is a genetically heterogenic, structural disorder of the glomerular basement membrane (GBM) due to the mutation of COL4A3, COL4A4, or…”
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CLINICAL SIGNIFICANCE OF ZERO-TIME RENAL TRANSPLANT BIOPSIES AND THIN GLOMERULAR BASEMENT MEMBRANES IN ZERO-TIME RENAL TRANSPLANT BIOPSIES by Senjug, Petar, Horacek, Matija, Maksimovic, Bojana, Vucur, Ksenija, Horvatic, Ivica, Zagorec, Nikola, Knotek, Mladen, Ljubanovic, Danica Galesic

“…Aim. To investigate morphological findings of zero-time biopsies analyzed at the Department of Nephropathology and Electron Microscopy, Dubrava University…”
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ASSOCIATION OF THE AUTOANTIBODIES TO M-TYPE PHOSPHOLIPASE A2 RECEPTOR TITER WITH CLINICAL CHARACTERISTICS AND OUTCOME OF PATIENTS WITH PRIMARY MEMBRANOUS NEPHROPATHY - 5-YEAR FOLLOW UP STUDY by Laganovic, Mario, Horvatic, Ivica, Bubic, Ivan, Ilic, Mario, Maksimovic, Bojana, Kozmar, Ana, Brinar, Ivana Vukovic, Crnogorac, Matija, Zivko, Marijana, Fistrek, Margareta, Jurekovic, Zeljka, Ljubanovic, Danica Galesic, Coric, Marijana, Bulimbasic, Stela, Galesic, Kresimir, Knotek, Mladen

“…Introduction: primary membranous nephropathy (pMN) is glomerulopathy caused in the majority of cases by autoantibodies to Phospholipase-A2 receptors…”
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REPORT OF THE CROATIAN REGISTRY OF NATIVE KIDNEY BIOPSIES FOR YEAR 2019 by Laganovic, Mario, Gellineo, Lana, Bulimbasic, Stela, Sulc, Snjezana, Skegro, Dinko, Minazek, Marija, Barbic, Jerko, Margeta, Tea Vrdoljak, Bubic, Ivan, Dordevic, Gordana, Vidovic, Luka, Altabas, Karmela, Senjug, Petar, Ljubanovic, Danica Galesic, Dogas, Tina, Durdov, Merica Glavina, Radic, Josipa, Babic, Gordan, Gulin, Marijana, Vojkovic, Marina, Klaric, Dragan, Nakic, Dario, Kupres, Vlasta, Brinar, Ivana Vukovic, Coric, Marijana, Simundic, Tihana, Samardzija, Goran, Josipovic, Josipa, Gulin, Tonko, Sefer, Sinisa, Fodor, Ljiljana, Cingel, Branislav, Zibar, Lada, Gunjaca, Mihaela, Knotek, Mladen, Jelicic, Ivo, Luketin, Mirko, Brkovic, Tonci, Pavlovic, Petra Grbic, Santini, Danijela Dusevic, Dika, Zivka, Zivko, Marijana

“…Background: This report describes data collected by the Croatian Registry of Renal Biopsies (CRRB) for the year 2019. Patients and methods: nine centers (82%)…”
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IgA-mediated anti-glomerular basement membrane disease. A case report by Bacalja, Jasna, Zibar, Lada, Ljubanović, Danica Galešić

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De novo immune complex–mediated membranoproliferative glomerulonephritis after COVID-19 vaccination by Zagorec, Nikola, Bojić, Martin, Kasumović, Dino, Šenjug, Petar, Ljubanović, Danica Galešić, Galešić, Krešimir, Horvatić, Ivica

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Marcel Kornfeld – zaboravljeni patolog i cijenjeni učitelj by Kolić, Marko, Galešić Ljubanović, Danica

“…SAŽETAK Autori su u radu prikazali život i rad Marcela Kornfelda (1886. – 1937.), patologa i sveučilišnog nastavnika. U radu je kronološki prikazan Kornfeldov…”
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A glycine substitution in the collagenous domain of Col4a3 in mice recapitulates late onset Alport syndrome by Odiatis, Christoforos, Savva, Isavella, Pieri, Myrtani, Ioannou, Pavlos, Petrou, Petros, Papagregoriou, Gregory, Antoniadou, Kyriaki, Makrides, Neoklis, Stefanou, Charalambos, Ljubanović, Danica Galešić, Nikolaou, Georgios, Borza, Dorin-Bogdan, Stylianou, Kostas, Gross, Oliver, Deltas, Constantinos

“…Alport syndrome (AS) is a severe inherited glomerulopathy caused by mutations in the genes encoding the α-chains of type-IV collagen, the most abundant…”
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