Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Marie Engesser"'
Autor:
Jonathan de Fallois, Soeren Schenk, Jan Kowald, Tom H Lindner, Marie Engesser, Johannes Münch, Christof Meigen, Jan Halbritter
Publikováno v:
PLoS ONE, Vol 17, Iss 9, p e0273671 (2022)
BackgroundIn nephrotic range proteinuria of adult-onset, kidney biopsy is the diagnostic gold standard in determining the underlying cause of disease. However, in low grade or subnephrotic proteinuria the diagnostic value of kidney biopsy as first-li
Externí odkaz:
https://doaj.org/article/786ce5f9987e4a8ab40a38d13bb85692
Autor:
Jens Thiel, Marta Rizzi, Marie Engesser, Ann-Kathrin Dufner, Arianna Troilo, Raquel Lorenzetti, Reinhard E. Voll, Nils Venhoff
Publikováno v:
Arthritis Research & Therapy, Vol 19, Iss 1, Pp 1-7 (2017)
Abstract Background B cell depletion with rituximab (RTX) is approved for treatment of rheumatoid arthritis (RA) and ANCA-associated vasculitides (AAV). Recently, RTX has been shown to be effective in AAV maintenance therapy, but an optimal RTX treat
Externí odkaz:
https://doaj.org/article/2287e4d7dc8c4bdd8caad7ae30a18cbe
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 240:496-498
Publikováno v:
Klinische Monatsblätter für Augenheilkunde. 240:566-568
Autor:
Johannes Münch, Marie Engesser, Ria Schönauer, J Austin Hamm, Gulsen Akay, Beyhan Tüysüz, Toshihiko Shirakawa, Sumito Dateki, Laura Claus, Albertien M van Eerde, Timo Wagner, Carsten Bergmann, Jillian Buchan, Tara Wegner, Jennifer Posey, James R Lupski, Florence Petit, Andrew A Mccarthy, Gregory J Pazour, Cecilia W Lo, Bernt Popp, Jan Halbritter
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS Congenital anomalies of the kidney and urinary tract (CAKUT) represent the most common cause of chronic kidney failure in children. Despite growing knowledge of the genetic causes of CAKUT, the majority of cases remain etiological
Autor:
Johannes Münch, Marie Engesser, Ria Schönauer, J. Austin Hamm, Christin Hartig, Elena Hantmann, Gulsen Akay, Davut Pehlivan, Tadahiro Mitani, Zeynep Coban Akdemir, Beyhan Tüysüz, Toshihiko Shirakawa, Sumito Dateki, Laura R. Claus, Albertien M. van Eerde, Thomas Smol, Louise Devisme, Hélène Franquet, Tania Attié-Bitach, Timo Wagner, Carsten Bergmann, Anne Kathrin Höhn, Shirlee Shril, Ari Pollack, Tara Wenger, Abbey A. Scott, Sarah Paolucci, Jillian Buchan, George C. Gabriel, Jennifer E. Posey, James R. Lupski, Florence Petit, Andrew A. McCarthy, Gregory J. Pazour, Cecilia W. Lo, Bernt Popp, Jan Halbritter
Publikováno v:
Kidney Int
Congenital anomalies of the kidney and urinary tract (CAKUT) represent the most common cause of chronic kidney failure in children. Despite growing knowledge of the genetic causes of CAKUT, the majority of cases remain etiologically unsolved. Genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34b0ecdf2801d041ca44522885ccc64b
https://europepmc.org/articles/PMC10010616/
https://europepmc.org/articles/PMC10010616/
Publikováno v:
Journal of Renal Injury Prevention. 8:253-256
Following the recent publications of the STAR-study, the ASTRAL trial, the HERCULES trial and the CORAL trial on renal revascularization versus medical therapy in the management of atherosclerotic renovascular disease, there has been a near paradigm
Autor:
Jens Thiel, Marta Rizzi, Marie Engesser, Ann-Kathrin Dufner, Arianna Troilo, Raquel Lorenzetti, Reinhard E. Voll, Nils Venhoff
Publikováno v:
Arthritis Research & Therapy
Arthritis Research & Therapy, Vol 19, Iss 1, Pp 1-7 (2017)
Arthritis Research & Therapy, Vol 19, Iss 1, Pp 1-7 (2017)
Background B cell depletion with rituximab (RTX) is approved for treatment of rheumatoid arthritis (RA) and ANCA-associated vasculitides (AAV). Recently, RTX has been shown to be effective in AAV maintenance therapy, but an optimal RTX treatment sche