Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Anamarija Meglic"'
Autor:
Anamarija Meglic, Marusa Debeljak, Jernej Kovac, Alenka Trampus Bakija, Vladan Rajic, Nika Kojc, Katarina Trebusak Podkrajsek
Publikováno v:
Nefrología, Vol 40, Iss 4, Pp 421-428 (2020)
Background: Hereditary spherocytosis is clinically and genetically heterogeneous disorder and its clinical characteristics are spherocytosis, anaemia, jaundice and splenomegaly. The aetiology is associated to the genes encoding proteins involved in t
Externí odkaz:
https://doaj.org/article/90587a63775d40c2a850e5c835119e8a
Autor:
Nóra Garam, Marcell Cserhalmi, Zoltán Prohászka, Ágnes Szilágyi, Nóra Veszeli, Edina Szabó, Barbara Uzonyi, Attila Iliás, Christof Aigner, Alice Schmidt, Martina Gaggl, Gere Sunder-Plassmann, Dóra Bajcsi, Jürgen Brunner, Alexandra Dumfarth, Daniel Cejka, Stefan Flaschberger, Hana Flögelova, Ágnes Haris, Ágnes Hartmann, Andreas Heilos, Thomas Mueller, Krisztina Rusai, Klaus Arbeiter, Johannes Hofer, Dániel Jakab, Mária Sinkó, Erika Szigeti, Csaba Bereczki, Viktor Janko, Kata Kelen, György S. Reusz, Attila J. Szabó, Nóra Klenk, Krisztina Kóbor, Nika Kojc, Maarten Knechtelsdorfer, Mario Laganovic, Adrian Catalin Lungu, Anamarija Meglic, Rina Rus, Tanja Kersnik Levart, Ernesta Macioniene, Marius Miglinas, Anna Pawłowska, Tomasz Stompór, Ludmila Podracka, Michael Rudnicki, Gert Mayer, Romana Rysava, Jana Reiterova, Marijan Saraga, Tomáš Seeman, Jakub Zieg, Eva Sládková, Natasa Stajic, Tamás Szabó, Andrei Capitanescu, Simona Stancu, Miroslav Tisljar, Kresimir Galesic, András Tislér, Inga Vainumäe, Martin Windpessl, Tomas Zaoral, Galia Zlatanova, Mihály Józsi, Dorottya Csuka
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundFactor H-related protein 5 (FHR-5) is a member of the complement Factor H protein family. Due to the homology to Factor H, the main complement regulator of the alternative pathway, it may also be implicated in the pathomechanism of kidney d
Externí odkaz:
https://doaj.org/article/0c908e2545e94fcd87521ab9c91fb160
Autor:
Nóra Garam, Zoltán Prohászka, Ágnes Szilágyi, Christof Aigner, Alice Schmidt, Martina Gaggl, Gere Sunder-Plassmann, Dóra Bajcsi, Jürgen Brunner, Alexandra Dumfarth, Daniel Cejka, Stefan Flaschberger, Hana Flögelova, Ágnes Haris, Ágnes Hartmann, Andreas Heilos, Thomas Mueller, Krisztina Rusai, Klaus Arbeiter, Johannes Hofer, Dániel Jakab, Mária Sinkó, Erika Szigeti, Csaba Bereczki, Viktor Janko, Kata Kelen, György S. Reusz, Attila J. Szabó, Nóra Klenk, Krisztina Kóbor, Nika Kojc, Maarten Knechtelsdorfer, Mario Laganovic, Adrian Catalin Lungu, Anamarija Meglic, Rina Rus, Tanja Kersnik-Levart, Ernesta Macioniene, Marius Miglinas, Anna Pawłowska, Tomasz Stompór, Ludmila Podracka, Michael Rudnicki, Gert Mayer, Romana Rysava, Jana Reiterova, Marijan Saraga, Tomáš Seeman, Jakub Zieg, Eva Sládková, Tamás Szabó, Andrei Capitanescu, Simona Stancu, Miroslav Tisljar, Kresimir Galesic, András Tislér, Inga Vainumäe, Martin Windpessl, Tomas Zaoral, Galia Zlatanova, Dorottya Csuka
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-14 (2019)
Abstract Background Acquired or genetic abnormalities of the complement alternative pathway are the primary cause of C3glomerulopathy(C3G) but may occur in immune-complex-mediated membranoproliferative glomerulonephritis (IC-MPGN) as well. Less is kn
Externí odkaz:
https://doaj.org/article/69c3689758b34c40a3dddf8458dfe664
Publikováno v:
Clinical nephrology. 96(1)
Aims Autosomal recessive polycystic kidney disease (ARPKD) is a rare inherited disease. We reviewed the clinical characteristics, management, and outcomes in Slovenian pediatric patients with ARPKD. Materials and methods All patients with ARPKD who w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fba996b1d1ff30956a3ee0c87b116e1
https://pubmed.ncbi.nlm.nih.gov/34643492
https://pubmed.ncbi.nlm.nih.gov/34643492
Autor:
Attila Szabo, Barbara Uzonyi, Ágnes Szilágyi, Krešimir Galešić, Dóra Bajcsi, Gere Sunder-Plassmann, Mária Sinkó, Ernesta Macioniene, Anna Pawłowska, Nóra Klenk, Johannes Hofer, Marcell Cserhalmi, Klaus Arbeiter, Tanja Kersnik-Levart, Marius Miglinas, Dorottya Csuka, Ágnes Hartmann, Galia Zlatanova, Kata Kelen, Tomáš Seeman, Andreas Heilos, Marijan Saraga, Eva Sládková, Krisztina Rusai, Gert Mayer, Martin Windpessl, Erika Szigeti, Jana Reiterova, Ludmila Podracka, Nóra Veszeli, Edina Szabó, Martina Gaggl, Mario Laganović, Tamás Szabó, Tomasz Stompór, Stefan Flaschberger, Daniel Cejka, Rina Rus, Nika Kojc, Maarten Knechtelsdorfer, Nóra Garam, Miroslav Tisljar, András Tislér, Michael A. Rudnicki, Christof Aigner, Ágnes Haris, Natasa Stajic, Anamarija Meglic, Hana Flögelová, Jürgen Brunner, Simona Stancu, György Reusz, Attila Iliás, Jakub Zieg, Adrian Catalin Lungu, Viktor Janko, Thomas Mueller, Dániel Jakab, Inga Vainumäe, Krisztina Kóbor, Tomas Zaoral, Mihály Józsi, Csaba Bereczki, Romana Rysava, Alice Schmidt, Andrei Capitanescu, Zoltán Prohászka, Alexandra Dumfarth
Background: Factor H-related-5 (FHR-5) is a member of the complement Factor H protein family. Due to the homology to Factor H, the main complement regulator of the alternative pathway, it may also be implicated in pathomechanism of kidney diseases wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3aa783b1d7de2a6da574f817148d4831
https://doi.org/10.21203/rs.3.rs-32618/v1
https://doi.org/10.21203/rs.3.rs-32618/v1
Autor:
Matjaž Kopač, Anamarija Meglič
Publikováno v:
Slovenska pediatrija, Vol 30, Iss 4, Pp 214-220 (2023)
Lower urinary tract dysfunction is clinically relevant because it may cause urinary tract infections, mainly due to accumulation of residual urine, adversely affect renal function, and may cause urine incontinence that strongly affects the child’s
Externí odkaz:
https://doaj.org/article/59221ab929bd42388ce354c2f8e6adcd
Autor:
Anamarija Meglič, Matjaž Kopač
Publikováno v:
Slovenska pediatrija, Vol 30, Iss 4, Pp 222-230 (2023)
Disfunkcija spodnjih sečil, ki je tesno povezana z disfunkcijo črevesa, pomeni nepravilnosti v delovanju sečnega mehurja in sečnice. Različne vrste disfunkcije spodnjih sečil delimo glede na simptome in glede na vzrok, v katerega je usmerjeno z
Externí odkaz:
https://doaj.org/article/483b31344b69460380f149f0b32148a9
Publikováno v:
Slovenska pediatrija, Vol 30, Iss 4, Pp 171-175 (2023)
Okužbe sečil uvrščamo med pogostejše bakterijske okužbe pri dojenčkih in otrocih. Najpogostejši povzročitelj je bakterija Escherichia coli. V prispevku opisujemo pomembne razlike med kliničnim potekom akutne okužbe sečil pri dojenčkih, m
Externí odkaz:
https://doaj.org/article/512a7174f5434beb891defe84282a4b4
Publikováno v:
Slovenska pediatrija, Vol 30, Iss 4, Pp 249-254 (2023)
Ensuring unimpeded urine drainage from the upper portion of the urinary tract system, specifically the renal pelvis, is achieved through a temporary measure known as percutaneous nephrostomy. This procedure is most commonly employed in small children
Externí odkaz:
https://doaj.org/article/44e6fda7351c4af0a1b7cae2c1b249cc
Autor:
Matjaž Kopač, Anamarija Meglič
Publikováno v:
Slovenska pediatrija, Vol 30, Iss 4, Pp 214-220 (2023)
Disfunkcija spodnjih sečil je klinično pomembna, ker lahko povzroča okužbe sečil zaradi zastajanja urina v sečnem mehurju, negativno vpliva na delovanje ledvic in povzroča uhajanje urina s posledično pomembnim zmanjšanjem kakovosti otrokoveg
Externí odkaz:
https://doaj.org/article/69119c543ff449699d95c1b82a9810bd