Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tanja Knüppel"'
Autor:
Tanja Knüppel, Martin Konrad, Stefanie Weber, Franz Schaefer, Otto Mehls, Karl Schärer, Peter Schwaderer
Publikováno v:
Pediatric Nephrology. 23:251-256
A small fraction of patients with initial steroid-sensitive nephrotic syndrome (SSNS) develops late steroid resistance, i.e. a lack of remission after 4 weeks of relapse treatment despite previous response to steroids. The pathophysiological basis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65215436809c5c4adcf3db0066b50658
https://doi.org/10.1007/s00467-007-0653-5
https://doi.org/10.1007/s00467-007-0653-5
Autor:
Tanja Knüppel, Franz Schaefer, Stefanie Weber, Rüdiger Waldherr, Burkhard Tönshoff, Britta Höcker
Publikováno v:
Pediatric Nephrology. 21:1476-1479
Mutations in the NPHS2 gene, which encodes podocin, are associated with steroid-resistant nephrotic syndrome in childhood. Renal histology frequently presents focal segmental glomerulosclerosis (FSGS). Post-transplant recurrence of proteinuria in pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::730b838930569edf8436f547bcb96005
https://doi.org/10.1007/s00467-006-0148-9
https://doi.org/10.1007/s00467-006-0148-9
Autor:
Tanja Knüppel, Franz Schaefer, Stefanie Weber, Aysin Bakkaloglu, Martin Konrad, Elke Wühl, Corinne Antignac, Velibor Tasic, Predrag Miljkovic, Eva-Maria Schönfelder
Publikováno v:
American Journal of Kidney Diseases. 47:1004-1012
Background: Renal hypodysplasia, characterized by a decrease in nephron number, small overall kidney size, and maldeveloped renal tissue, is a leading cause of chronic renal failure in young children. Familial clustering and renal hypodysplasia pheno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::299e3bac3eb19f039fe408e915f600dd
https://doi.org/10.1053/j.ajkd.2006.02.177
https://doi.org/10.1053/j.ajkd.2006.02.177
Autor:
Dirk E. Müller-Wiefel, Jing Wang, Carsten Bergmann, Sergey Yaklichkin, Agnes Trautmann, Stefanie Weber, Tanja Knüppel, Richard G. Pestell, Raphael Schild, Martin Konrad, Kongming Wu, Franz Schaefer, Markus J. Kemper
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 28(1)
Renal hypodysplasia (RHD) is characterized by small and/or disorganized kidneys following abnormal organogenesis. Mutations in several genes have been identified recently to be associated with RHD in humans, including BMP4, a member of the transformi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21ae14ea29e0512e966dd9220aa4cc6f
https://pubmed.ncbi.nlm.nih.gov/23262432
https://pubmed.ncbi.nlm.nih.gov/23262432
Autor:
Marina Charbit, Jiri Dusek, Elke Wühl, Stefanie Weber, Aleksandra Zurowska, Amira Peco-Antic, Giovanni Montini, Sevgi Mir, Tanja Knüppel, Otto Mehls, Vincent Morinière, Corinne Antignac, Gian Marco Ghiggeri, Franz Schaefer, Augustina Jankauskiene, Rémi Salomon
Publikováno v:
Journal of the American Society of Nephrology : JASN. 17(10)
Renal hypodysplasia (RHD) is characterized by a reduced nephron number, small kidney size, and disorganized renal tissue. A hereditary basis has been established for a subset of affected patients, suggesting a major role of developmental genes that a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb796938c3fe081fb922f9cc6a42fb28
https://pubmed.ncbi.nlm.nih.gov/16959822
https://pubmed.ncbi.nlm.nih.gov/16959822