Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Dirk E. Mueller-Wiefel"'
Background. Prognosis of fetuses with renal oligohydramnios (ROH) is often still regarded as poor. Neonatal complications and the long-term follow-up of fetuses with ROH in two pediatric centres are described. Method. 23 fetuses (16 males, 7 females)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66d176506e677fe96134833d22d9e989
http://doc.rero.ch/record/295136/files/gfl591.pdf
http://doc.rero.ch/record/295136/files/gfl591.pdf
Autor:
Lars Pape, Heiko Billing, Jörg Dötsch, Lutz T. Weber, Sandra Habbig, Anne Rosahl, Martin Pohl, Katalin Dittrich, Katrin Rosenthal, Ludwig Patzer, Therese Jungraithmayr, Rafael T. Krmar, Jutta Gellermann, Markus J. Kemper, Dirk E. Mueller-Wiefel
Publikováno v:
Nephrology Dialysis Transplantation. 27:1910-1915
Background. In patients with refractory steroid-sensitive nephrotic syndrome (SSNS), treatment with rituximab has shown encouraging results; however, long-term follow-up data are not available. Methods. We performed a retrospective analysis of 37 pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3211a34c3ca6579c66ac69b04c853d5
https://doi.org/10.1093/ndt/gfr548
https://doi.org/10.1093/ndt/gfr548
Autor:
Eberhard Kuwertz-Broeking, Catharina Renken, Carsten Bergmann, Lars Pape, Horst Nizze, Christopher J. Ward, Dieter Haffner, Dagmar-Christiane Fischer, Ulrike Jacoby, Birgit Rudolph, Dirk E. Mueller-Wiefel, Uwe Querfeld
Publikováno v:
Nephrology Dialysis Transplantation. 24:1819-1827
BACKGROUND: Autosomal recessive polycystic kidney disease (ARPKD) [MIM 263200] belongs to a group of congenital hepatorenal fibrocystic syndromes and is caused by mutations in the PKHD1 gene encoding the multidomain protein fibrocystin/polyductin (FP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbef6ee884fc94e33076f260558647e2
https://doi.org/10.1093/ndt/gfn744
https://doi.org/10.1093/ndt/gfn744
Publikováno v:
European Journal of Pediatrics. 166:393-398
Although clinical outcome data on fetuses with oligohydramnios of renal origin are scarce, prognosis is regarded as poor due to a high risk of renal dysfunction and pulmonary hypoplasia. This review aims to summarize the current knowledge and clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75ca8b8b2267b375bc11b6ba6d1fba7b
https://doi.org/10.1007/s00431-006-0368-9
https://doi.org/10.1007/s00431-006-0368-9
Autor:
Thomas Neuhaus, Eberhard Kuwertz-Broeking, Dirk E. Mueller-Wiefel, Monika Bulla, Markus J. Kemper
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 19(5)
Background. In patients with steroid-dependent nephrotic syndrome (SDNS), long-term remission (LTR) can usually be achieved with cyclosporin A (CSA), after alternative treatment with cytotoxic drugs or levamisole has failed. Nevertheless, severe SDNS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e2a627faa48b8ef116c9b80ddf33a81
https://pubmed.ncbi.nlm.nih.gov/14993510
https://pubmed.ncbi.nlm.nih.gov/14993510
Autor:
Tobias Obser, Johannes Häberle, Wolf A Hassenpflug, Karl-Walter Sykora, Volker Aumann, Dorothea Angerhaus, Karim Kentouche, Florian Oyen, Karin Kurnik, Elke Drewke, Reinhard Schneppenheim, Elisabeth Kohne, Dirk E Mueller-Wiefel, René Santer, Ulrich Budde
Publikováno v:
Blood. 101(5)
Thrombotic thrombocytopenic purpura (TTP) is caused by the persistence of the highly reactive high-molecular-weight multimers of von Willebrand factor (VWF) due to deficiency of the specific VWF-cleaving protease (VWF-CP) ADAMTS13, resulting in micro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f2f49b661c38b79f096b2b9a5c8f5e
https://pubmed.ncbi.nlm.nih.gov/12393505
https://pubmed.ncbi.nlm.nih.gov/12393505
Publikováno v:
Nephrology Dialysis Transplantation; Feb2007, Vol. 22 Issue 2, p432-439, 8p
Autor:
Markus J. Kemper, Eberhard Kuwertz-Broeking, Monika Bulla, Dirk E. Mueller-Wiefel, Thomas J. Neuhaus
Publikováno v:
Nephrology Dialysis Transplantation; May2004, Vol. 19 Issue 5, p1136-1141, 6p