Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Anja K Büscher"'
Autor:
Stefanie Jeruschke, Kay Jeruschke, Andrew DiStasio, Sinem Karaterzi, Anja K Büscher, Perihan Nalbant, Ludger Klein-Hitpass, Peter F Hoyer, Jürgen Weiss, Rolf W Stottmann, Stefanie Weber
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137043 (2015)
Glomerular podocytes are highly differentiated cells that are key components of the kidney filtration units. The podocyte cytoskeleton builds the basis for the dynamic podocyte cytoarchitecture and plays a central role for proper podocyte function. R
Externí odkaz:
https://doaj.org/article/a717350a9c5046bfa105ee797e497590
Bone health in children with primary hyperoxaluria type 1 following liver and kidney transplantation
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundPrimary hyperoxaluria type 1 is characterized by hepatic oxalate overproduction, leading to nephrocalcinosis, kidney stones, kidney failure and systemic oxalosis, including oxalate osteopathy. Combined liver-kidney transplantation (CLKT) an
Externí odkaz:
https://doaj.org/article/b0c81269397f4f2a86d9908bddbedc7f
Autor:
Sarina Butzer, Imke Hennies, Charlotte Gimpel, Jutta Gellermann, Gesa Schalk, Sabine König, Anja K. Büscher, Anja Lemke, Martin Pohl
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background IgA vasculitis (IgAV) is the most common form of systemic vasculitis in childhood and frequently involves the kidney. A minority of patients with IgA vasculitis nephritis (IgAVN), especially those presenting with heavy proteinuria
Externí odkaz:
https://doaj.org/article/6fb6d99858354840862069921b6d5e85
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionThe number of children with acute and chronic liver disease is rising. Moreover, liver involvement may be limited to subtle changes in organ texture especially in early childhood and some syndromic conditions, such as ciliopathies. Attenu
Externí odkaz:
https://doaj.org/article/aba94a9fafce4fe1a555e0508c21c9fe
Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age
Autor:
Roman Günthner, Lea Knipping, Stefanie Jeruschke, Robin Satanoskij, Bettina Lorenz-Depiereux, Clara Hemmer, Matthias C. Braunisch, Korbinian M. Riedhammer, Jasmina Ćomić, Burkhard Tönshoff, Velibor Tasic, Nora Abazi-Emini, Valbona Nushi-Stavileci, Karin Buiting, Nikola Gjorgjievski, Ana Momirovska, Ludwig Patzer, Martin Kirschstein, Oliver Gross, Adrian Lungu, Stefanie Weber, Lutz Renders, Uwe Heemann, Thomas Meitinger, Anja K. Büscher, Julia Hoefele
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
X-linked Alport syndrome (AS) caused by hemizygous disease-causing variants in COL4A5 primarily affects males. Females with a heterozygous state show a diverse phenotypic spectrum ranging from microscopic hematuria to end-stage kidney disease (ESKD)
Externí odkaz:
https://doaj.org/article/b7bb8aa91fa849b0bfdf65d2e43b6deb
Autor:
Frederik, Stephan, Hanjo, Groetschel, Anja K, Büscher, Deniz, Serdar, Kjell A, Groes, Rainer, Büscher
Publikováno v:
Journal of paediatrics and child health. 54(9)
The outcome of children with an out-of-hospital cardiac arrest is still poor, but bystander cardiopulmonary resuscitation can increase survival and minimise severe neurological sequelae. While teaching basic life support is standardised in emergency
Autor:
Kerstin Amann, Anja K. Büscher, Christoph Licht, Martin Pohl, Magdalena Riedl, Stefanie Weber, Lutz T. Weber
Publikováno v:
Nierenerkrankungen im Kindes-und Jugendalter ISBN: 9783662487884
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5b76f1fdd787220c93a9868649aed4b
https://doi.org/10.1007/978-3-662-48789-1_2
https://doi.org/10.1007/978-3-662-48789-1_2
Autor:
Rainer, Büscher, Dominik, Nagel, Ilja, Finkelberg, Anja K, Büscher, Anne-Margret, Wingen, Birgitta, Kranz, Udo, Vester, Peter F, Hoyer
Publikováno v:
Pediatric transplantation. 15(2)
Genetic polymorphisms of the RAS correlate with allograft function. We therefore analyzed common RAS polymorphisms in kidney donors and in children following RTx to determine the relationship between genotype and decline in GFR, blood pressure, and L
Autor:
Marvin Droste, Tobias Tertel, Stefanie Jeruschke, Robin Dittrich, Evangelia Kontopoulou, Bernd Walkenfort, Verena Börger, Peter F. Hoyer, Anja K. Büscher, Basant K. Thakur, Bernd Giebel
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 22, p 12436 (2021)
Small extracellular vesicles isolated from urine (uEVs) are increasingly recognized as potential biomarkers. Meanwhile, different uEV preparation strategies exist. Conventionally, the performance of EV preparation methods is evaluated by single parti
Externí odkaz:
https://doaj.org/article/804edd60f6b8494487c34634acd43f45