Zobrazeno 1 - 10
of 57
pro vyhledávání: '"c3gn"'
Akademický článek
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Publikováno v:
European Journal of Medical Research, Vol 26, Iss 1, Pp 1-9 (2021)
Abstract Background Alport syndrome and C3 glomerulonephritis (C3GN) are rare kidney diseases, frequently responsible for familial haematuria, proteinuria, and renal impairment. With the rapid development of molecular genetic testing, Alport syndrome
Externí odkaz:
https://doaj.org/article/2149d92fab214212a627e261c611245b
Autor:
Leszek Niepolski, Anna Czekała, Monika Seget-Dubaniewicz, Magdalena Frydrychowicz, Patrycja Talarska-Markiewicz, Angelika Kowalska, Jagoda Szmelter, Wiesława Salwa-Żurawska, Tomasz Sirek, Dawid Sobański, Beniamin Oskar Grabarek, Jakub Żurawski
Publikováno v:
Biomedicines, Vol 11, Iss 4, p 1101 (2023)
Background: C3 glomerulopathies (C3GN) are a group of rare kidney diseases associated with impaired complement regulation. The effects of this disease include the accumulation of complement C3 in the kidneys. Based on the clinical data, as well as li
Externí odkaz:
https://doaj.org/article/e18791aa1cad4d588568bb8feb85cd72
Publikováno v:
Renal Failure, Vol 43, Iss 1, Pp 1437-1445 (2021)
Objective To investigate the demographic and clinicopathological features and renal outcomes of Chinese patients with C3 glomerulonephritis in the setting of monoclonal gammopathy. Methods Patients with renal biopsy-proven C3 glomerulonephritis and d
Externí odkaz:
https://doaj.org/article/5d58aff810054a9786f798e0d2757ad5
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:
Giacomo Quattrocchio, Antonella Barreca, Antonella Vaccarino, Giulio Del Vecchio, Emanuele De Simone, Roberta Fenoglio, Michela Ferro, Maria Pagliaro, Massimo Pini, Massimo Manes, Dario Roccatello
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Monoclonal Gammopathy of Renal Significance (MGRS) is a group of heterogeneous disorders characterized by renal dysfunction secondary to the production of a monoclonal immunoglobulin by a nonmalignant B cell or plasma cell clone. We report the clinic
Externí odkaz:
https://doaj.org/article/37685e693abf43a199e9673714a20046
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Renal Failure
article-version (VoR) Version of Record
Renal Failure, Vol 43, Iss 1, Pp 1437-1445 (2021)
article-version (VoR) Version of Record
Renal Failure, Vol 43, Iss 1, Pp 1437-1445 (2021)
Objective To investigate the demographic and clinicopathological features and renal outcomes of Chinese patients with C3 glomerulonephritis in the setting of monoclonal gammopathy. Methods Patients with renal biopsy-proven C3 glomerulonephritis and d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::344bdfc6bd72e5e7cbe036ace8af0360
https://pubmed.ncbi.nlm.nih.gov/34658305
https://pubmed.ncbi.nlm.nih.gov/34658305
Autor:
Piero Ruggenenti, Erica Daina, Alessia Gennarini, Camillo Carrara, Sara Gamba, Marina Noris, Nadia Rubis, Francesco Peraro, Flavio Gaspari, Andrea Pasini, Angelo Rigotti, Renelda M. Lerchner, Domenico Santoro, Antonio Pisani, Alessandra Pasi, Giuseppe Remuzzi, G. Remuzzi, P. Ruggenenti, E. Mondo, S. Rota, C. Carrara, V. Portalupi, A. Pasini, G. Monitini, E. Monti, A. Rigotti, F. De Giovanni, B. Giacon, R.M. Lerchner, W. Passler, D. Santoro, L. Visconti, A. Pisani, E. Riccio, A. Pasi, M. Dugo, C. Tuono, F. Emma, M. Vivarelli, L. Murer, E. Benetti, R. Coppo, A. Amore, G. Gambaro, S. Passalacqua, B. Ruggiero, E. Daina, E. Bresin, S. Gamba, S. Prandini, V. Lecchi, D. Cugini, G. Gherardi, N. Rubis, O. Diadei, A. Villa, D. Villa, P. Boccardo, S. Peracchi, D. Martinetti, A. Perna, F. Peraro, G.A. Giuliano, F. Gaspari, F. Carrara, S. Ferrari, N. Stucchi, A. Cannata, M. Noris, S. Bettoni, M. Alberti, P. Cuccarolo, P. Rizzo, G.F. Marchetti, A. Sonzogni
Publikováno v:
American Journal of Kidney Diseases. 74:224-238
Rationale & Objective: Primary membranoproliferative glomerulonephritis (MPGN) is a rare glomerulopathy characterized by complement dysregulation. MPGN progresses rapidly to kidney failure when it is associated with nephrotic syndrome. We assessed th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc7b70a33652892fcfdf5a7495a36899
https://doi.org/10.1053/j.ajkd.2018.12.046
https://doi.org/10.1053/j.ajkd.2018.12.046