Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Tanja Wlodkowski"'
Autor:
Loes Oomen, Liesbeth L. De Wall, Kai Krupka, Burkhard Tönshoff, Tanja Wlodkowski, Loes FM Van Der Zanden, Marjolein Bonthuis, Ilse D. Duus Weinreich, Linda Koster-Kamphuis, Wout FJ Feitz, Charlotte MHHT Bootsma-Robroeks
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionPatient data are increasingly available in (multi)national registries, especially for rare diseases. This study aims to provide an overview of current European registries of paediatric kidney transplantation (PKT) care, their coverage, an
Externí odkaz:
https://doaj.org/article/40542666d08946e48d2b42b290d86881
Autor:
Giulia Bassanese, Tanja Wlodkowski, Aude Servais, Laurence Heidet, Dario Roccatello, Francesco Emma, Elena Levtchenko, Gema Ariceta, Justine Bacchetta, Giovambattista Capasso, Augustina Jankauskiene, Marius Miglinas, Pietro Manuel Ferraro, Giovanni Montini, Jun Oh, Stephane Decramer, Tanja Kersnik Levart, Jack Wetzels, Elisabeth Cornelissen, Olivier Devuyst, Aleksandra Zurowska, Lars Pape, Anja Buescher, Dieter Haffner, Natasa Marcun Varda, Gian Marco Ghiggeri, Giuseppe Remuzzi, Martin Konrad, Germana Longo, Detlef Bockenhauer, Atif Awan, Ilze Andersone, Jaap W. Groothoff, Franz Schaefer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background The European Rare Kidney Disease Reference Network (ERKNet) recently established ERKReg, a Web-based registry for all patients with rare kidney diseases. The main objectives of this core registry are to generate epidemiological in
Externí odkaz:
https://doaj.org/article/298d7b2d56344d9ab3fa1ca68f07142f
Autor:
Mansoureh Tabatabaeifar, Tanja Wlodkowski, Ivana Simic, Helga Denc, Geraldine Mollet, Stefanie Weber, John Julius Moyers, Barbara Brühl, Michael Joseph Randles, Rachel Lennon, Corinne Antignac, Franz Schaefer
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0186574 (2017)
Mutations in the NPHS2 gene, encoding podocin, cause hereditary nephrotic syndrome. The most common podocin mutation, R138Q, is associated with early disease onset and rapid progression to end-stage renal disease. Knock-in mice carrying a R140Q mutat
Externí odkaz:
https://doaj.org/article/15990f0e8a694b30833228b2d7898f65
Autor:
Matko Marlais, Tanja Wlodkowski, Nikoleta Printza, Dorothea Kronsteiner, Regina Krisam, Lukas Sauer, Marina Aksenova, Isa Ashoor, Atif Awan, Justine Bacchetta, Ramnath Balasubramanian, Biswanath Basu, Zivile Bekassy, Olivia Boyer, Eugene Yu-hin Chan, Dagmar Csaicsich, Stéphane Decramer, Eiske Dorresteijn, Magdalena Drozynska-Duklas, Loai Akram Eid, Laura Espinosa, Verónica Ferraris, Hana Flögelová, Jessica Forero-Delgadillo, Alessandra Gianviti, Valentina Gracchi, Mercedes López González, Matthias Hansen, Motoshi Hattori, Xu Hong, Nakysa Hooman, Dmytro Ivanov, Hee Gyung Kang, Vasiliki Karava, Ina Kazyra, Adrian Lungu, Stephen Marks, Andrew Maxted, Anna Moczulska, Rebekka Müller, Tatiana Nastausheva, Mattia Parolin, Carmine Pecoraro, Iliana Principi, Cheryl Sanchez-Kazi, Seha Saygili, Raphael Schild, Mohan Shenoy, Rajiv Sinha, Ana Paula Spizzirri, Maria Stack, Maria Szczepanska, Alexey Tsygin, Julia Tzeng, Vaidotas Urbonas, Carlos Zapata, Jakub Zieg, Franz Schaefer, Marina Vivarelli, Kjell Tullus
Publikováno v:
American Journal of Kidney Diseases, 81(1), 119-122. W B SAUNDERS CO-ELSEVIER INC
American Journal of Kidney Diseases, 81(1), 119-122. W.B. Saunders
American Journal of Kidney Diseases, 81(1), 119-122. W.B. Saunders
Autor:
Carla, Burballa, Gerard, Cantero-Recasens, Larisa, Prikhodina, Francesca, Lugani, Karlpeter, Schlingmann, Petr V, Ananin, Martine, Besouw, Detlef, Bockenhauer, Leire, Madariaga, Aurelia, Bertholet-Thomas, Francesca, Taroni, Mattia, Parolin, Peter, Conlon, Dorella, Delprete, Dominique, Chauveau, Linda, Koster-Kamphuis, Marc, Fila, Andrea, Pasini, Isabel, Castro, Giacomo, Colussi, Marta, Gil, Barian, Mohidin, Tanja, Wlodkowski, Franz, Schaefer, Gema, Ariceta, Monica, Duran
Publikováno v:
Nephrology dialysis transplantation, Oxford : Oxford University Press, 2023, vol. 38, iss. 6, p. 1497-1507
Nephrology, Dialysis, Transplantation, 38, 1497-1507
Nephrology, Dialysis, Transplantation, 38, 6, pp. 1497-1507
Nephrology, Dialysis, Transplantation, 38, 1497-1507
Nephrology, Dialysis, Transplantation, 38, 6, pp. 1497-1507
Background Dent's disease type 1 (DD1) is a rare X-linked nephropathy caused by CLCN5 mutations, characterized by proximal tubule dysfunction, including low molecular weight proteinuria (LMWP), hypercalciuria, nephrolithiasis–nephrocalcinosis, prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4faae0b874db4c1776378f0b22526ff0
https://hdl.handle.net/11577/3474373
https://hdl.handle.net/11577/3474373
Autor:
Max C. Liebau, Olivia Boyer, Rosa Vargas-Poussou, Jun Oh, Bahriye Atmis, Tanja Wlodkowski, Maria VanDyck, Elena Levtchenko, Amina Talhi, Umut Selda Bayrakci, Nur Canpolat, Maria Gema Ariceta Iraola, Loai A. Eid, Fernando Santos, Bağdagül Aksu, Selçuk Yüksel, Rezan Topologlu, Franz Schaefer, Carlos Moguel, Marc Fila, Sergio Camilo Lopez-Garcia, Nakisa Homan, Detlef Bockenhauer, Svetlana Papizh, Francesco Emma
Publikováno v:
Nephrology Dialysis Transplantation. 36
Background and Aims Distal renal tubular acidosis (dRTA) is a rare disorder characterised by an inability of the distal tubule to secrete acid, leading to metabolic acidosis. Clinical consequences typically include hypokalaemia, hypercalciuria with n
Autor:
Pietro Manuel Ferraro, Rosa Vargas-Poussou, Martin Konrad, Rezan Topaloglu, Francesco Trepiccione, Velibor Tasic, Fernando Santos, Gema Ariceta, Elena Levtchenko, Tanja Wlodkowski, Maria Szczepańska, Dieter Haffner, Stella Stabouli, Sergio Camilo Lopez-Garcia, Olivia Boyer, Detlef Bockenhauer, Roberta Camilla, Francesco Emma, Steven B. Walsh
Distal renal tubular acidosis (dRTA) is characterized by an impaired ability of the distal tubule to excrete acid, leading to metabolic acidosis. Associated complications include bone disease, growth failure, urolithiasis and hypokalaemia. Due to its
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::710124252711c230428d44ae62327906
https://lirias.kuleuven.be/handle/20.500.12942/691461
https://lirias.kuleuven.be/handle/20.500.12942/691461
Autor:
Pietro Manuel Ferraro, Elena Levtchenko, Tanja Kersnik Levart, Jaap W. Groothoff, Olivier Devuyst, Giovanni Montini, Anja Buescher, Dario Roccatello, Justine Bacchetta, Francesco Emma, Jun Oh, Dieter Haffner, Elisabeth A.M. Cornelissen, Tanja Wlodkowski, Martin Konrad, Jack F.M. Wetzels, Natasa Marcun Varda, Gema Ariceta, Detlef Bockenhauer, Aleksandra Zurowska, Germana Longo, Augustina Jankauskiene, Aude Servais, Giuseppe Remuzzi, Ilze Andersone, Franz Schaefer, Laurence Heidet, Lars Pape, Stéphane Decramer, Giovambattista Capasso, Marius Miglinas, Gian Marco Ghiggeri, Giulia Bassanese, Atif Awan
Publikováno v:
Orphanet journal of rare diseases, London : BioMed Central Ltd., 2021, vol.16, no. 1, p. 1844-1859
Orphanet journal of rare diseases, 16(1):251. BioMed Central
Orphanet Journal of Rare Diseases, 16
Scientia
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Orphanet Journal of Rare Diseases, Vol. 16, no.1, p. 251 (2021)
Orphanet Journal of Rare Diseases, 16, 1
Orphanet journal of rare diseases, 16(1):251. BioMed Central
Orphanet Journal of Rare Diseases, 16
Scientia
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Orphanet Journal of Rare Diseases, Vol. 16, no.1, p. 251 (2021)
Orphanet Journal of Rare Diseases, 16, 1
Epidemiologia; Nefrologia pediàtrica; Registre Epidemiología; Nefrología pediátrica; Registro Epidemiology; Pediatric nephrology; Registry Background The European Rare Kidney Disease Reference Network (ERKNet) recently established ERKReg, a Web-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f580ddf5b1808b33370d6fb1bbd3079
https://www.ncbi.nlm.nih.gov/pubmed/34078418
https://www.ncbi.nlm.nih.gov/pubmed/34078418
Autor:
Kiran Upadhyay, Luciola Vásquez, Tanja Wlodkowski, Kjell Tullus, Anshuman Saha, Rajiv Sinha, Michiel F. Schreuder, Nakysa Hooman, Iftikhar Ijaz, Nivedita Pande, Marina Vivarelli, Dmitry Samsonov, Samhar I. Al-Akash, Petr Ananin, Olivia Boyer, Donald J. Weaver, Franz Schaefer, Sahar Siddiqui, Lars Pape, Reyner Loza, Robert P. Woroniecki, Sukanya Govindan, Heather Stewart, Varun Kumar Bandi, Véronique Baudouin, Marta Melgosa, Jyoti Sharma, Matko Marlais, Katherine Twombley, Burkhard Tönshoff, Velibor Tasic
Publikováno v:
Archives of Disease in Childhood
BackgroundChildren are recognised as at lower risk of severe COVID-19 compared with adults, but the impact of immunosuppression is yet to be determined. This study aims to describe the clinical course of COVID-19 in children with kidney disease takin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::096427126dea2a004a3ea68787d27c58
https://www.ncbi.nlm.nih.gov/pubmed/33355203
https://www.ncbi.nlm.nih.gov/pubmed/33355203
Autor:
Nicole Kraewer, Betti Schaefer, Max C. Liebau, Christian Tischer, Gwendolyn Eich, Sebastian Pichl, Claus Peter Schmitt, Karel Vondrak, Tanja Wlodkowski, Bruno Ranchin, Maria Bartosova, Thilo Hackert
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 12, p e0189903 (2017)
PLoS ONE, Vol 12, Iss 12, p e0189903 (2017)
Background Ultrafiltration decline is a progressive issue for patients on chronic peritoneal dialysis (PD) and can be caused by peritoneal angiogenesis induced by PD fluids. A recent pediatric trial suggests better preservation of ultrafiltration wit