Zobrazeno 1 - 10
of 99
pro vyhledávání: '"Stajić Nataša"'
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 152, Iss 3-4, Pp 182-185 (2024)
Introduction. Coronavirus disease-2019 (COVID-19) usually leads to a mild infectious disease course in children, but serious neurological complications have been described in association with both acute infection and the multisystem inflammatory synd
Externí odkaz:
https://doaj.org/article/b3ef188f9f2c45e9890372041a9b65c0
Autor:
Vujić Ana, Obradović Slobodan, Igrutinović Zoran, Protrka Zoran, Janković Marijana, Radovanović Marija, Stajić Nataša, Medović Raša, Janković Sveta
Publikováno v:
Vojnosanitetski Pregled, Vol 80, Iss 3, Pp 270-274 (2023)
Introduction. Schimke immuno-osseous dysplasia (SIOD) is a rare autosomal recessive multisystem disorder associated with biallelic mutations of the SMAR-CAL1 gene. Vascular central nervous system complications in the form of Moyamoya syndrome (MMS) h
Externí odkaz:
https://doaj.org/article/0a3c5301e0e74ed5952de6bae93b3b5d
Autor:
Kuzmanović Miloš, Kunishima Shinji, Putnik Jovana, Stajić Nataša, Paripović Aleksandra, Bogdanović Radovan
Publikováno v:
Vojnosanitetski Pregled, Vol 71, Iss 4, Pp 395-398 (2014)
Introduction. The group of autosomal dominant disorders - Epstein syndrome, Sebastian syndrome, Fechthner syndrome and May-Hegglin anomaly - are characterised by thrombocytopenia with giant platelets, inclusion bodies in granulocytes and variable
Externí odkaz:
https://doaj.org/article/21f798b39714438589be6169b2f409f0
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 140, Iss 5-6, Pp 313-320 (2012)
Introduction. Chronic kidney disease (CKD) is a significant cause of morbidity and mortality in paediatric population. Objective. The aim of the study was analysis of aetiology, staging and associated complications of CKD at the time of diagnosis. Me
Externí odkaz:
https://doaj.org/article/3efb115735ce4479b9f4b69ba4fb0aba
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
Externí odkaz:
https://doaj.org/article/a68f3f0ef01f4739be9f975dc8354f3d
Autor:
Sovtić Aleksandar, Minić Predrag, Bogdanović Radovan, Stajić Nataša, Rodić Milan, Marković-Sovtić Gordana
Publikováno v:
Vojnosanitetski Pregled, Vol 69, Iss 4, Pp 367-369 (2012)
Introduction. 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
Externí odkaz:
https://doaj.org/article/8f1b5bcf051d413cac626853de657d45
Autor:
Bogdanović Radovan, Kuzmanović Miloš, Marković-Lipkovski Jasmina, Ognjanović Miloš, Mićić Dragan, Stanković Ivica, Stajić Nataša, Nikolić Vesna, Bunjevački Gordana
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 130, Iss 9-10, Pp 323-328 (2002)
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
Externí odkaz:
https://doaj.org/article/a20c32e439ed4f39853ff6fe8dd31e13
Autor:
Morimoto Marie, Yu Zhongxin, Stenzel Peter, Clewing J, Najafian Behzad, Mayfield Christy, Hendson Glenda, Weinkauf Justin G, Gormley Andrew K, Parham David M, Ponniah Umakumaran, André Jean-Luc, Asakura Yumi, Basiratnia Mitra, Bogdanović Radovan, Bokenkamp Arend, Bonneau Dominique, Buck Anna, Charrow Joel, Cochat Pierre, Cordeiro Isabel, Deschenes Georges, Fenkçi M, Frange Pierre, Fründ Stefan, Fryssira Helen, Guillen-Navarro Encarna, Keller Kory, Kirmani Salman, Kobelka Christine, Lamfers Petra, Levtchenko Elena, Lewis David B, Massella Laura, McLeod D, Milford David V, Nobili François, Saraiva Jorge M, Semerci C, Shoemaker Lawrence, Stajić Nataša, Stein Anja, Taha Doris, Wand Dorothea, Zonana Jonathan, Lücke Thomas, Boerkoel Cornelius F
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 70 (2012)
Abstract Background Arteriosclerosis and emphysema develop in individuals with Schimke immuno-osseous dysplasia (SIOD), a multisystem disorder caused by biallelic mutations in SMARCAL1 (SWI/SNF-related, matrix-associated, actin-dependent regulator of
Externí odkaz:
https://doaj.org/article/d09043e0cde94048b164e22867785031
Autor:
Wu, Chen-Han Wilfred, Lim, Tze Y., Wang, Chunyan, Seltzsam, Steve, Zheng, Bixia, Schierbaum, Luca, Schneider, Sophia, Mann, Nina, Connaughton, Dervla M., Nakayama, Makiko, van der Ven, Amelie T., Dai, Rufeng, Kolvenbach, Caroline M., Kause, Franziska, Ottlewski, Isabel, Stajic, Natasa, Soliman, Neveen A., Kari, Jameela A., El Desoky, Sherif, Fathy, Hanan M., Milosevic, Danko, Turudic, Daniel, Al Saffar, Muna, Awad, Hazem S., Eid, Loai A., Ramanathan, Aravind, Senguttuvan, Prabha, Mane, Shrikant M., Lee, Richard S., Bauer, Stuart B., Lu, Weining, Hilger, Alina C., Tasic, Velibor, Shril, Shirlee, Sanna-Cherchi, Simone, Hildebrandt, Friedhelm
Publikováno v:
In European Urology Open Science October 2022 44:106-112
Autor:
Paripović, Aleksandra, Stajić, Nataša, Putnik, Jovana, Gazikalović, Ana, Bogdanović, Radovan, Vladislav, Vukomanović
Publikováno v:
In Nephrologie et Thérapeutique December 2020 16(7):420-423