Zobrazeno 1 - 10
of 272
pro vyhledávání: '"Peco-Antić Amira"'
Autor:
Mulat Simachew Yonas, Mihajlović Marija, Antonić Tamara, Miloševski-Lomić Gordana, Peco-Antić Amira, Jovanović Dragana, Paripović Dušan, Stefanović Aleksandra
Publikováno v:
Journal of Medical Biochemistry, Vol 43, Iss 3, Pp 424-435 (2024)
Background: The pathophysiological mechanisms crucial in the development of nephrotic syndrome (NS) in the pediatric population are still not fully understood. This study aimed to investigate the relationship between hypertension, oxidative stress, a
Externí odkaz:
https://doaj.org/article/581a6b127cc04f34b1e9e22ffa28cd96
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 152, Iss 1-2, Pp 81-84 (2024)
Introduction. Congenital nephrotic syndrome (CNS) is a severe disease complicated by hemodynamic instability, infections, thrombosis, growth disorder and progressive renal failure leading to end-stage kidney disease within a few years. The mutations
Externí odkaz:
https://doaj.org/article/498b39466bca4ace8d7f411b4b0a9a60
Autor:
Peco-Antić Amira, Mulić Bilsana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 148, Iss 9-10, Pp 631-636 (2020)
Podocytopathies include a wide spectrum of primary or secondary glomerular diseases that are the consequence of the podocyte injuries. The damage of podocytes can occur due to congenital or acquired disorders of podocyte transcriptional regulators, a
Externí odkaz:
https://doaj.org/article/4b46bb550ee64d828da646a973c04d3a
Autor:
Peco-Antić Amira
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 146, Iss 3-4, Pp 218-225 (2018)
Pediatric renal stone disease is manifested as nephro/urolithiasis (UL) and/or nephrocalcinosis (NC). Compared to adults, UL in childhood is less common, and it is believed to be around 5% in industrialized countries, while the incidence of NC is
Externí odkaz:
https://doaj.org/article/485aa9e5ec5c4256bc1cf165b06d4b2e
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 146, Iss 1-2, Pp 77-80 (2018)
Introduction. Recently, inactivation mutations of CYP24A1, the gene encoding vitamin D 24-hydroxylase, were identified in hypercalciuric nephrolithiasis and nephrocalcinosis. Here, we describe а long-term follow-up of a patient with hypercalciuric n
Externí odkaz:
https://doaj.org/article/9300614d39fb456eb1310bda5e88d2f2
Autor:
Peco-Antić Amira, Kostić Mirjana, Spasojević Brankica, Miloševski-Lomić Gordana, Paripović Dušan, Kruščić Divna, Cvetković Mirjana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 145, Iss 3-4, Pp 147-152 (2017)
Introduction/Objective. Jeune syndrome (JS) is a rare hereditary ciliopathy characterized by asphyxiating thoracic dystrophy, shortened limbs and brachydactyly. Extraskeletal anomalies such as chronic renal failure (CRF), hepatic fibrosis, and retini
Externí odkaz:
https://doaj.org/article/a6876651e8d9418aa3799037b224fa04
Autor:
Mulić Bilsana, Miloševski-Lomić Gordana, Paripović Dušan, Kruščić Divna, Mulić Mersudin, Peco-Antić Amira
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 145, Iss 7-8, Pp 407-410 (2017)
Introduction. Congenital nephrotic syndrome (CNF) is manifested at birth or within the first three months of life. The Finnish-type of CNF is caused by the mutation of the NPHS1 gene, which encodes nephrin in the podocyte slit diaphragm. It is a very
Externí odkaz:
https://doaj.org/article/669d1740b8b8431998283b9fe92e745c
Autor:
Stefanović Aleksandra, Ristovski-Kornic Danijela, Kotur-Stevuljević Jelena, Spasojević-Kalimanovska Vesna, Vekić Jelena, Miljković Milica, Paripović Dušan, Peco-Antić Amira, Jelić-Ivanović Zorana, Zeljković Aleksandra
Publikováno v:
Journal of Medical Biochemistry, Vol 36, Iss 4, Pp 358-365 (2017)
Background: Unfavorable lipid profile presents one of most important risk factor for cardiovascular disease in renal pathology. Myeloperoxidase (MPO) as enzyme which oxidizes lipoproteins and paraoxonase1 (PON1) as anti-oxidative enzyme have been inv
Externí odkaz:
https://doaj.org/article/0be44f44cf544d2780e26735acc83262
Autor:
Ristovski-Kornic Danijela, Stefanović Aleksandra, Kotur-Stevuljević Jelena, Zeljković Aleksandra, Spasojević-Kalimanovska Vesna, Vekić Jelena, Miljković Milica, Paripović Dušan, Peco-Antić Amira, Jelić-Ivanović Zorana
Publikováno v:
Journal of Medical Biochemistry, Vol 36, Iss 1, Pp 23-31 (2017)
Background: The aim of this study was to explore oxidative stress status, especially the enzyme myeloperoxidase in children with end-stage renal disease. Also, we investigated possible associations between the atherogenic index of plasma and these pa
Externí odkaz:
https://doaj.org/article/ae241385cbb048ec8105b96e1e472162
Autor:
Peco-Antić Amira
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 144, Iss 11-12, Pp 664-669 (2016)
The hemolytic-uremic syndrome (HUS) is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury (AKI). The major cause of HUS in childhood (>90%) is infection with verocytotoxin (Shiga-like toxin - “Stx”)-p
Externí odkaz:
https://doaj.org/article/ab81fd31524f4bd6a631ffdf48027883