Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Jeroen K.J. Deegens"'
Autor:
Sander Groen in ’t Woud, Ilse M. Rood, Eric Steenbergen, Brigith Willemsen, Henry B. Dijkman, Michel van Geel, Jeroen Schoots, Jack F.M. Wetzels, Dorien Lugtenberg, Jeroen K.J. Deegens, Ernie M.H.F. Bongers
Publikováno v:
Kidney Medicine, Vol 5, Iss 4, Pp 100607- (2023)
Rationale & Objective: Mono-allelic variants in COL4A3 and COL4A4 (COL4A3/COL4A4) have been identified in a spectrum of glomerular basement membrane nephropathies, including thin basement membrane nephropathy and autosomal dominant Alport syndrome. W
Externí odkaz:
https://doaj.org/article/e2543628cf3a44b4b7497f8486a0754e
Autor:
Jeroen K.J. Deegens, Ilse M. Rood, Dorien Lugtenberg, Aernoud Bavinck, Jack F.M. Wetzels, Beata S. Lipska-Ziętkiewicz, Franz Schaefer
Publikováno v:
Kidney International Reports, 7, 1, pp. 87-98
Kidney International Reports, 7, 87-98
Kidney International Reports
Kidney International Reports, 7, 87-98
Kidney International Reports
Introduction Guidelines advise initial therapy with corticosteroids (CSs) in patients with presumed primary focal segmental glomerular sclerosis (pFSGS). Many patients do not achieve complete remission (CR) after 8 or 16 weeks. Although these patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dd3836fa42141fad22bc2a05b184b1b
https://doi.org/10.1016/j.ekir.2021.10.016
https://doi.org/10.1016/j.ekir.2021.10.016
Autor:
Ernie M.H.F. Bongers, Dorien Lugtenberg, Jeroen K.J. Deegens, Jack F.M. Wetzels, Ilse M. Rood
Publikováno v:
American Journal of Kidney Diseases, 73, 3, pp. 400-403
American Journal of Kidney Diseases, 73, 400-403
American Journal of Kidney Diseases, 73, 400-403
Mutations in the NPHS2 gene, which encodes the podocyte slit diaphragm protein podocin, cause autosomal recessive steroid-resistant nephrotic syndrome (Online Mendelian Inheritance in Man [OMIM] #600995). Basic research and clinical studies have prov
Autor:
Tom Nijenhuis, Jack F.M. Wetzels, Rutger J. Maas, Cansu Yanginlar, Johan van der Vlag, Dirk J W den Braanker, Jeroen K.J. Deegens
Publikováno v:
Nephrology, Dialysis, Transplantation, 36, 247-256
Nephrology, Dialysis, Transplantation, 36, 2, pp. 247-256
Nephrology, Dialysis, Transplantation, 36, 2, pp. 247-256
Background Many patients with idiopathic focal segmental glomerulosclerosis (FSGS) develop recurrence of proteinuria after kidney transplantation (TX). Although several circulating permeability factors (CPFs) responsible for recurrence have been sugg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82846ac0397e38faa709b958df6e4494
https://doi.org/10.1093/ndt/gfaa211
https://doi.org/10.1093/ndt/gfaa211
Autor:
Susan Coventry, Michelle T. Barati, Michael L. Merchant, Jack F.M. Wetzels, Kenneth R. McLeish, Laura H. Mariani, Jeroen K.J. Deegens, Michael E. Brier, Matthias Kretzler, Dawn J. Caster, Liliane Hobeika, Ilse M. Rood, Christopher P. Larsen, Jessica Hata, Daniel W. Wilkey, Ming Li, Jeffrey B. Hodgin, Jon B. Klein, Jonathan P. Troost
Publikováno v:
J Am Soc Nephrol
Journal of the American Society of Nephrology, 31, 8, pp. 1883-1904
Journal of the American Society of Nephrology, 31, 1883-1904
Journal of the American Society of Nephrology, 31, 8, pp. 1883-1904
Journal of the American Society of Nephrology, 31, 1883-1904
Background The mechanisms leading to extracellular matrix (ECM) replacement of areas of glomerular capillaries in histologic variants of FSGS are unknown. This study used proteomics to test the hypothesis that glomerular ECM composition in collapsing
Autor:
Manuja Kaluarachchi, Joram M. Posma, Jack F.M. Wetzels, Ilse M. Rood, Claire L. Boulangé, Elaine Holmes, Jeroen K.J. Deegens, John C. Lindon
Publikováno v:
Molecular Omics, 15, 1, pp. 39-49
Molecular Omics, 15, 39-49
Molecular Omics, 15, 39-49
Nephrotic syndrome with idiopathic membranous nephropathy as a major contributor, is characterized by proteinuria, hypoalbuminemia and oedema. Diagnosis is based on renal biopsy and the condition is treated using immunosuppressive drugs; however neph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee7c7183976a559f3946b1b0e6024e0d
http://hdl.handle.net/10044/1/71111
http://hdl.handle.net/10044/1/71111
Autor:
Toin H. van Kuppevelt, Brigith Willemsen, Jeroen K.J. Deegens, Markus A. Loeven, Sandrine Florquin, Jennifer Eymael, Marinka A.H. Bakker, Johan van der Vlag, Marcus J. Moeller, Tammo Ostendorf, Jack F.M. Wetzels, Vikram Sharma, Fieke Mooren, Henry B.P.M. Dijkman, Shagun Sharma, Bart Smeets
Publikováno v:
Kidney International, 93, 626-642
Kidney International, 93, 3, pp. 626-642
Kidney international, 93(3), 626-642. Nature Publishing Group
Kidney International, 93, 3, pp. 626-642
Kidney international, 93(3), 626-642. Nature Publishing Group
A key feature of glomerular diseases such as crescentic glomerulonephritis and focal segmental glomerulosclerosis is the activation, migration and proliferation of parietal epithelial cells. CD44-positive activated parietal epithelial cells have been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4bb3f07aabe9ec1a26475dd23994920
https://doi.org/10.1016/j.kint.2017.09.020
https://doi.org/10.1016/j.kint.2017.09.020
Publikováno v:
American Journal of Transplantation, 17, 5, pp. 1160-1166
American Journal of Transplantation
American Journal of Transplantation, 17, 1160-1166
American Journal of Transplantation
American Journal of Transplantation, 17, 1160-1166
Urine represents a noninvasive source in which proteins and nucleic acids can be assessed. Such analytes may function as biomarkers to monitor kidney graft pathology at every desired frequency, thereby providing a time window to prevent graft damage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47d34df1cf5d00809a32891df7f7ee81
https://doi.org/10.1111/ajt.14082
https://doi.org/10.1111/ajt.14082
Autor:
Jack F.M. Wetzels, A. Warmold L. van den Wall Bake, Jeroen K.J. Deegens, Willi H. Van Kuijk, Rutger J. Maas, Daniel A. Geerse, Pieter L. Rensma, Johan R. Beukhof, Marc A.G.J. ten Dam, C.J.A.M. Konings, Geert W. Feith, L.J.M. Reichert, J.J. Beutler
Publikováno v:
American Journal of Kidney Diseases, 69, 5, pp. 637-646
American Journal of Kidney Diseases, 69, 637-646
American Journal of Kidney Diseases, 69, 637-646
Contains fulltext : 174168.pdf (Publisher’s version ) (Closed access) BACKGROUND: Few studies have examined the treatment and outcome of adult-onset minimal change nephrotic syndrome (MCNS). We retrospectively studied 125 patients who had MCNS with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4873f6358dec57b0bf938607f0f783b1
https://hdl.handle.net/2066/174168
https://hdl.handle.net/2066/174168
Publikováno v:
Nature Reviews. Nephrology, 13, 731-749
Nature Reviews. Nephrology, 13, 12, pp. 731-749
Nature Reviews. Nephrology, 13, 12, pp. 731-749
Item does not contain fulltext Urine is a valuable diagnostic medium and, with the discovery of urinary extracellular vesicles, is viewed as a dynamic bioactive fluid. Extracellular vesicles are lipid-enclosed structures that can be classified into t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::622bada57ce641f095bf2f6d74fdda4b
http://hdl.handle.net/2066/182516
http://hdl.handle.net/2066/182516