Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Divna Kruscic"'
Autor:
Mirjana Kostic, Amira Peco-Antic, Brankica Spasojevic, Mirjana Cvetkovic, Divna Kruscic, Gordana Milosevski-Lomic, Dusan Paripovic
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
Autor:
Bilsana Mulic, Gordana Milosevski-Lomic, Amira Peco-Antic, Dusan Paripovic, Divna Kruscic, Mersudin Mulic
Publikováno v:
Srpski arhiv za celokupno lekarstvo (2017) 145(7-8):407-410
Srpski Arhiv za Celokupno Lekarstvo, Vol 145, Iss 7-8, Pp 407-410 (2017)
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
Autor:
Gordana Milosevski-Lomic, Dusan Paripovic, Zoran Krstic, Brankica Spasojević-Dimitrijeva, Amira Peco-Antic, Mirjana Kostic, Mirjana Cvetkovic, Divna Kruscic, Maja Čupić
Publikováno v:
Srpski arhiv za celokupno lekarstvo (2014) 142(1-2):83-88
Srpski Arhiv za Celokupno Lekarstvo, Vol 142, Iss 1-2, Pp 83-88 (2014)
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 is m
Autor:
K. van Hoeck, Khadizha Emirova, Karlijn J. van Stralen, J.M. des Grottes, G. von Gersdorff, Kitty J. Jager, C. Afonso, O. Berbeca, Vidar O. Edvardsson, Diamant Shtiza, D. Roussinov, L. Backmän, Jadranka Buturović-Ponikvar, Polina Miteva, Stefano Picca, Tamás Szabó, Anastasios Kapogiannis, Paloma Maria Parvex, Staffan Schön, B. Rippe, Ludmila Podracka, Conceição Mota, Aleksandra Zurowska, Ilona Zagozdzon, Sibylle Tschumi, S. Gatcan, Mirjana Kostic, Gordana Milosevski-Lomic, Enrico Vidal, Natalia Tomilina, N. Abazi, Valerie Said-Conti, Guido F. Laube, Ana Sánchez-Moreno, Runolfur Palsson, Marjolein Bonthuis, A. Cassula, Dusan Paripovic, Brigitte Adams, A. Sukalo, Anna Bjerre, A. Alonso Melgar, S. Puric, Jérôme Harambat, D. Pokrajac, Antal Szabó, N. Zaikova, Aysun Karabay Bayazit, Frederic Collart, Cécile Couchoud, Aline C. Hemke, Boris Bikbov, B. Höcker, Nina Battelino, Karel Vondrak, S. Rudaitis, D. Batinić, Carmine Pecoraro, F. Braddon, Gabriel Mircescu, M. Lemac, Marie Evans, Brankica Spasojević-Dimitrijeva, N. Ristoka Bojkovska, Sergey Baiko, Torbjørn Leivestad, Silvio Maringhini, C.E. Kuenhi, R. Pruthi, Christoph J. Mache, S. Mannings, Franz Schaefer, Andries J. Hoitsma, Elisabeth Maurer, Tomáš Seeman, Gregor Novljan, Augustina Jankauskiene, Enrico Verrina, Rezan Topaloglu, José Eduardo Esteves Da Silva, Antonella Trivelli, R. Oberbauer, Lars Pape, Nikolaos Afentakis, Bruno Gianoglio, M. Lasalle, K. Krupka, Nicholas C. Chesnaye, Gabriel Kolvek, Jaap W. Groothoff, Christer Holmberg, Nikoleta Printza, James G. Heaf, Eva Kis, S. Pavićević, Patrik Finne, C. Scholz, Maria Stendahl, Divna Kruscic, C.S. Berecki, Manish D. Sinha, Carola Grönhagen-Riska, J. Slavicek, Z.S. Györke, Amira Peco-Antic, Emilija Sahpazova, M. Almeida, Burkhard Tönshoff, Karl G. Prütz, G Reusz, Elena A. Molchanova, D. Ivanov, Maria Herthelius, Reinhard Kramar, Sara Testa, U. Toots, Liliana Garneata
Publikováno v:
American Journal of Kidney Diseases, Vol. 69, No 5 (2017) pp. 617-625
Background: The impact of different dialysis modalities on clinical outcomes has not been explored in young infants with chronic kidney failure. Study Design: Cohort study. Setting & Participants: Data were extracted from the ESPN/ERA-EDTA Registry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2379f48b750e257a9206322f2fefde9
https://hdl.handle.net/10668/10671
https://hdl.handle.net/10668/10671
Autor:
Gordana Milosevski-Lomic, Mirjana Cvetković, Dusan Paripovic, Brankica Spasojević-Dimitrijeva, Amira Peco-Antic, Divna Kruscic, Mirjana Kostic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 139, Iss 3-4, Pp 174-178 (2011)
Introduction. Henoch-Sch?nlein purpura (HSP) is the most common vasculitis of childhood. It is characterized by symptoms including nonthrombocytopenic purpura, abdominal pain, haematuria/proteinuria, and arthralgia/arthritis. The pleiomorphism of cli
Autor:
Mirjana Cvetković, Amira Peco-Antic, Mirjana Kostic, Dusan Paripovic, Divna Kruscic, Brankica Spasojević-Dimitrijeva, Gordana Milosevski-Lomic
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 138, Iss 3-4, Pp 197-203 (2010)
Introduction. Growth retardation is a hallmark of chronic illnesses such as chronic kidney disease in children, and it is associated with increased morbidity and mortality. The growth hormone (GH) resistance observed in uraemia can be overcome by sup
Publikováno v:
Pediatric Nephrology. 24:1165-1172
The aim of our study was to examine diurnal variation in urine volume (UV) output, proteinuria (UPRT), urine creatinine (UCr) and urine sodium ion excretion (UNa) in children with chronic glomerulopathy. In 56 patients (20 boys/36 girls, aged 11.7 +/
Publikováno v:
Pediatric Nephrology. 21:437-440
Renal artery stenosis (RAS) is one of the most common causes of severe arterial hypertension in infants. Its management is very difficult, especially when present in a single kidney. We report a case of severe hypertension caused by RAS of congenital
Autor:
Babić D, Divna Kruscic, Jovanović O, Amira Peco-Antic, Mirjana Kostic, Mirjana Stanic, Gordana Milosevski
Publikováno v:
Srpski Arhiv za Celokupno Lekarstvo, Vol 133, Iss 9-10, Pp 417-423 (2005)
INTRODUCTION Renal scarring is the most common cause of arterial hypertension in children. High blood pressure (BP) and microalbuminuria contribute to the progression of chronic renal disease. OBJECTIVE The aims of the study were: to assess BP in chi
Autor:
Jovanović O, Mirjana Kostic, Maja Živković, Dragan Alavantić, Aleksandra Stanković, Amira Peco-Antic, Divna Kruscic
Publikováno v:
Pediatric Nephrology
Scopus-Elsevier
Scopus-Elsevier
The objective of this study was to investigate whether DNA polymorphisms of the renin-angiotensin system (RAS) genes were associated with renal scar formation in pediatric patients with bladder dysfunction (BD). Although these children are born healt