Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jonathan de Fallois"'
Autor:
Max Braune, Moritz Metelmann, Jonathan de Fallois, Christian Pfrepper, Alonso Barrantes-Freer, Grit Gesine Ruth Hiller, Susette Unger, Evelyn Seelow, Jan Halbritter, Johann Otto Pelz
Publikováno v:
Neurological Research and Practice, Vol 6, Iss 1, Pp 1-11 (2024)
Abstract Background Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (RVCL-S) is an ultra-rare, autosomal-dominant small vessel disease caused by loss-of-function variants in the gene TREX1. Recently, elevated serum
Externí odkaz:
https://doaj.org/article/bae7f95c918f4696baccd5ec50aa0d89
Autor:
Jonathan de Fallois, Robert Scharm, Tom H. Lindner, Christina Scharf, Sirak Petros, Lorenz Weidhase
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-13 (2024)
Abstract Background Toxic renal effects of myoglobin following rhabdomyolysis can cause acute kidney injury (AKI) with the necessity of kidney replacement therapy (KRT). Fast elimination of myoglobin seems notable to save kidney function and intensif
Externí odkaz:
https://doaj.org/article/3660d29c23214bbf813ab29b8bb61f87
Autor:
Lotte Scherer, Ria Schönauer, Melanie Nemitz-Kliemchen, Tobias Hagemann, Elena Hantmann, Jonathan de Fallois, Friederike Petzold, Matthias Blüher, Jan Halbritter
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract The risk of enteric hyperoxaluria is significantly increased after malabsorptive bariatric surgery (MBS). However, its underlying determinants are only poorly characterized. In this case–control study, we aimed at identifying clinical and
Externí odkaz:
https://doaj.org/article/a679c7e6b1334e9d8ca4e54b82d1b783
Autor:
Claudia Lehmann, Sarah Pehnke, Antje Weimann, Anette Bachmann, Katalin Dittrich, Friederike Petzold, Daniel Fürst, Jonathan de Fallois, Ramona Landgraf, Reinhard Henschler, Tom H. Lindner, Jan Halbritter, Ilias Doxiadis, Bernt Popp, Johannes Münch
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionAntibody mediated rejection (ABMR) is the most common cause of long-term allograft loss in kidney transplantation (KT). Therefore, a low human leukocyte antigen (HLA) mismatch (MM) load is favorable for KT outcomes. Hitherto, serological
Externí odkaz:
https://doaj.org/article/14a0bf85605c46498eb42a53c1a6bc98
Autor:
Dana Sierks, Ria Schönauer, Anja Friedrich, Elena Hantmann, Jonathan de Fallois, Nikolas Linder, Janett Fischer, Adam Herber, Carsten Bergmann, Thomas Berg, Jan Halbritter
Publikováno v:
JHEP Reports, Vol 4, Iss 11, Pp 100579- (2022)
Background & Aims: Polycystic liver disease (PLD) manifests as numerous fluid-filled cysts scattered throughout the liver parenchyma. PLD most commonly develops in females, either as an extra-renal manifestation of autosomal-dominant polycystic kidne
Externí odkaz:
https://doaj.org/article/b8d51ffe40c4400a8346b121ecbd8216
Autor:
Lorenz Weidhase, Jonathan de Fallois, Elena Haußig, Thorsten Kaiser, Meinhard Mende, Sirak Petros
Publikováno v:
Critical Care, Vol 24, Iss 1, Pp 1-12 (2020)
Abstract Background Myoglobin clearance in acute kidney injury requiring renal replacement therapy is important because myoglobin has direct renal toxic effects. Clinical data comparing different modalities of renal replacement therapy addressing myo
Externí odkaz:
https://doaj.org/article/26c2571075e049c2984747a24b49c3ba
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
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
BackgroundAutosomal polycystic kidney disease is distinguished into dominant (ADPKD) and recessive (ARPKD) inheritance usually caused by either monoallelic (PKD1/PKD2) or biallelic (PKHD1) germline variation. Clinical presentations are genotype-depen
Externí odkaz:
https://doaj.org/article/5756729c649b46ea956ecce862df4f2a
Autor:
Lorenz Weidhase, Elena Haussig, Stephan Haussig, Thorsten Kaiser, Jonathan de Fallois, Sirak Petros
Publikováno v:
PLoS ONE, Vol 14, Iss 4, p e0215823 (2019)
BackgroundRegional anticoagulation with citrate during renal replacement therapy (RRT) reduces the risk of bleeding, extends dialyzer lifespan and is cost-effective. Therefore, current guidelines recommend its use if patients are not anticoagulated f
Externí odkaz:
https://doaj.org/article/c9270418cd8b4f449516bf003b3f4bdf
Autor:
Schmalz, Dandan Ren, Thomas Ebert, Deborah Kreher, Bero Luke Vincent Ernst, Jonathan de Fallois, Gerhard
Publikováno v:
Genes; Volume 14; Issue 7; Pages: 1374
Periodontitis and chronic kidney failure (CKF) are potentially related to each other. This bioinformatics analysis aimed at the identification of potential cross-talk genes and related pathways between periodontitis and CKF. Based on NCBI Gene Expres