Congenital nephrotic syndrome may respond to cyclosporine A: A case report and review of literature

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)

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://explore.openaire.eu/search/publication?articleId=doi_dedup___::a216aec15563e7d9058e25514b4ee028
http://scindeks.ceon.rs/article.aspx?artid=0370-81791708407M

Infants Requiring Maintenance Dialysis: Outcomes of Hemodialysis and Peritoneal Dialysis

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

Recombinant human growth hormone treatment in short children with renal disease: Our first experience

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e4a56045f0bb31140e8be44128fb503
http://www.doiserbia.nb.rs/img/doi/0370-8179/2010/0370-81791004197S.pdf

Severe renovascular hypertension in an infant with congenital solitary pelvic kidney

Autor: Milan Djukic, Amira Peco-Antic, Zoran Krstic, Divna Kruscic, Dragan Sagic

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88e3553ad3d5186a3ca33dae145d20cb
https://doi.org/10.1007/s00467-005-2109-0

ACE and AT1 receptor gene polymorphisms and renal scarring in urinary bladder dysfunction

Autor: Jovanović O, Mirjana Kostic, Maja Živković, Dragan Alavantić, Aleksandra Stanković, Amira Peco-Antic, Divna Kruscic

Publikováno v: Pediatric Nephrology
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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a68f74b6db30b506d4a102ba180e5daf
https://doi.org/10.1007/s00467-004-1511-3