Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Miloševski-Lomić Gordana"'
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 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:
Miloševski-Lomić Gordana, Marković-Lipkovski Jasmina, Kostić Mirjana, Paripović Dušan, Spasojević-Dimitrijeva Brankica, Peco-Antić Amira
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 144, Iss 3-4, Pp 215-218 (2016)
Introduction. The causes of acute tubulointerstitial nephritis can be grouped into four broad categories: medications, infections, immunologic diseases, or idiopathic processes. Here we report a 17-year-old female who developed acute kidney injury
Externí odkaz:
https://doaj.org/article/9385d53513aa41a6b7d181b0cbb89f3a
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 143, Iss 3-4, Pp 219-225 (2015)
A normal development of lower urinary tract function control evolves from involuntary bladder empting (incontinence) during infancy to daytime urinary continence, and finally a successful day and night continence that is generally achieved by the
Externí odkaz:
https://doaj.org/article/525d51fd9e474921bf36628d78e206ac
Autor:
Pavlović Branko, Milosavljević Jovana, Zeljković Aleksandra, Vekić Jelena, Joksić Jelena, Sopić Miron, Spasojević-Kalimanovska Vesna, Paripović Dušan, Peco-Antić Amira, Miloševski-Lomić Gordana, Jelić-Ivanović Zorana
Publikováno v:
Arhiv za farmaciju, Vol 65, Iss 2, Pp 115-128 (2015)
Introduction: Childhood obesity is related to cardiovascular diseases and diabetes mellitus type 2 in later life. Resistin, an adipokine primarily secreted by monocytes and tissue macrophages in humans, is considered to be associated with these condi
Externí odkaz:
https://doaj.org/article/4d716753214541fc8a9f77c218ace5dd
Autor:
Spasojević-Dimitrijeva Brankica, Peco-Antić Amira, Paripović Dušan, Kruščić Divna, Krstić Zoran, Čupić Maja, Cvetković Mirjana, Miloševski-Lomić Gordana, Kostić Mirjana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 142, Iss 1-2, Pp 83-88 (2014)
Introduction. Post-transplant lymphoproliferative disorder (PTLD) is a heterogeneous group of diseases, characterized by abnormal lymphoid proliferation following transplantation. It is a disease of the immunosuppressed state, and its occurrence i
Externí odkaz:
https://doaj.org/article/5adb58df0546421e8633b3cd79acc4de
Autor:
Peco-Antić Amira, Ozaltin Fatih, Parezanović Vojislav, Miloševski-Lomić Gordana, Zdravković Verica
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 141, Iss 9-10, Pp 685-688 (2013)
Introduction. Frasier syndrome (FS) is a genetic form of glomerulopathy, which results from mutations in the Wilms’ tumour suppressor gene (WT1). Proteinuria in FS has been traditionally considered unresponsive to any medication and FS inevitably p
Externí odkaz:
https://doaj.org/article/a1e0eaf318384852972d6a061434f66a
Autor:
Peco-Antić Amira, Paripović Dušan, Buljugić Svetlana, Kruščić Divna, Spasojević Brankica, Cvetković Mirjana, Kostić Mirjana, Laban-Nestorović Suzana, Miloševski-Lomić Gordana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 140, Iss 3-4, Pp 179-183 (2012)
Introduction. Urinary tract infection is common in childhood. Depending on the localization of the infection, severity of its clinical presentation and possible acute and long-term complications, it may be described as either acute cystitis or acute
Externí odkaz:
https://doaj.org/article/9ff8615299ba45a9868fa7a181f9bd38