Real-world data of six patients with atypical hemolytic uremic syndrome switched to ravulizumab

por Ehren, Rasmus, Habbig, Sandra
Publicado 2021

Ciliopathies - from rare inherited cystic kidney diseases to basic cellular function

por Habbig, Sandra, Liebau, Max Christoph
Publicado 2015

Molecular causes of congenital anomalies of the kidney and urinary tract (CAKUT)

por Kohl, Stefan, Habbig, Sandra, Weber, Lutz T., Liebau, Max C.
Publicado 2021

Complement activation in children with Streptococcus pneumoniae associated hemolytic uremic syndrome

por Holle, Johannes, Habbig, Sandra, Gratopp, Alexander, Mauritsch, Anna, Müller, Dominik, Thumfart, Julia
Publicado 2021

Loss of Dgcr8-mediated microRNA expression in the kidney results in hydronephrosis and renal malformation

por Bartram, Malte P, Dafinger, Claudia, Habbig, Sandra, Benzing, Thomas, Schermer, Bernhard, Müller, Roman-Ulrich
Publicado 2015

Differential assessment of fluid compartments by bioimpedance in pediatric patients with kidney diseases

por Frey, Sandra M., Vogt, Bruno, Simonetti, Giacomo D., Büscher, Rainer, Habbig, Sandra, Schaefer, Franz
Publicado 2021

The role of the FSGS disease gene product and nuclear pore protein NUP205 in regulating nuclear localization and activity of transcriptional regulators YAP and TAZ

por Ester, Lioba, Cabrita, Inês, Ventzke, Michel, Kieckhöfer, Emilia, Christodoulou, Marita, Mandel, Amrei M, Diefenhardt, Paul, Fabretti, Francesca, Benzing, Thomas, Habbig, Sandra, Schermer, Bernhard
Publicado 2023

C3-Glomerulopathy Autoantibodies Mediate Distinct Effects on Complement C3- and C5-Convertases

por Zhao, Fei, Afonso, Sara, Lindner, Susanne, Hartmann, Andrea, Löschmann, Ina, Nilsson, Bo, Ekdahl, Kristina N., Weber, Lutz T., Habbig, Sandra, Schalk, Gesa, Kirschfink, Michael, Zipfel, Peter F., Skerka, Christine
Publicado 2019

cfNOMe — A single assay for comprehensive epigenetic analyses of cell-free DNA

por Erger, Florian, Nörling, Deborah, Borchert, Domenica, Leenen, Esther, Habbig, Sandra, Wiesener, Michael S., Bartram, Malte P., Wenzel, Andrea, Becker, Christian, Toliat, Mohammad R., Nürnberg, Peter, Beck, Bodo B., Altmüller, Janine
Publicado 2020

Hyperuricemia Is an Early and Relatively Common Feature in Children with HNF1B Nephropathy but Its Utility as a Predictor of the Disease Is Limited

por Kołbuc, Marcin, Bieniaś, Beata, Habbig, Sandra, Kołek, Mateusz F., Szczepańska, Maria, Kiliś-Pstrusińska, Katarzyna, Wasilewska, Anna, Adamczyk, Piotr, Motyka, Rafał, Tkaczyk, Marcin, Sikora, Przemysław, Beck, Bodo B., Zaniew, Marcin
Publicado 2021

NPHP4, a cilia-associated protein, negatively regulates the Hippo pathway

por Habbig, Sandra, Bartram, Malte P., Müller, Roman U., Schwarz, Ricarda, Andriopoulos, Nikolaos, Chen, Shuhua, Sägmüller, Josef G., Hoehne, Martin, Burst, Volker, Liebau, Max C., Reinhardt, H. Christian, Benzing, Thomas, Schermer, Bernhard
Publicado 2011

Humoral immune response and live-virus neutralization of the SARS-CoV-2 omicron (BA.1) variant after COVID-19 mRNA vaccination in children and young adults with chronic kidney dise...

por Stich, Maximilian, Di Cristanziano, Veronica, Tönshoff, Burkhard, Weber, Lutz Thorsten, Dötsch, Jörg, Rammer, Marian Theodor, Rieger, Susanne, Heger, Eva, Garbade, Sven F., Burgmaier, Kathrin, Benning, Louise, Speer, Claudius, Habbig, Sandra, Haumann, Sophie
Publicado 2022

Expanding the Spectrum of FAT1 Nephropathies by Novel Mutations That Affect Hippo Signaling

por Fabretti, Francesca, Tschernoster, Nikolai, Erger, Florian, Hedergott, Andrea, Buescher, Anja K., Dafinger, Claudia, Reusch, Bjoern, Köntges, Vincent K., Kohl, Stefan, Bartram, Malte P., Weber, Lutz Thorsten, Thiele, Holger, Altmueller, Janine, Schermer, Bernhard, Beck, Bodo B., Habbig, Sandra
Publicado 2021

Nephrocystin-4 Regulates Pyk2-induced Tyrosine Phosphorylation of Nephrocystin-1 to Control Targeting to Monocilia

por Liebau, Max C., Höpker, Katja, Müller, Roman U., Schmedding, Ingolf, Zank, Sibylle, Schairer, Benjamin, Fabretti, Francesca, Höhne, Martin, Bartram, Malte P., Dafinger, Claudia, Hackl, Matthias, Burst, Volker, Habbig, Sandra, Zentgraf, Hanswalter, Blaukat, Andree, Walz, Gerd, Benzing, Thomas, Schermer, Bernhard
Publicado 2011

Impaired Systolic and Diastolic Left Ventricular Function in Children with Chronic Kidney Disease - Results from the 4C Study

por Doyon, Anke, Haas, Pascal, Erdem, Sevcan, Ranchin, Bruno, Kassai, Behrouz, Mencarelli, Francesca, Lugani, Francesca, Harambat, Jerome, Matteucci, Maria Chiara, Chinali, Marcello, Habbig, Sandra, Zaloszyc, Ariane, Testa, Sara, Vidal, Enrico, Gimpel, Charlotte, Azukaitis, Karolis, Kovacevic, Alexander, Querfeld, Uwe, Schaefer, Franz
Publicado 2019

Arterial tissue transcriptional profiles associate with tissue remodeling and cardiovascular phenotype in children with end-stage kidney disease

por Freise, Christian, Schaefer, Betti, Bartosova, Maria, Bayazit, Aysun, Bauer, Ulrike, Pickardt, Thomas, Berger, Felix, Rasmussen, Lars Melholt, Jensen, Pia Søndergaard, Laube, Guido, Mencarelli, Francesca, Arbeiter, Klaus, Büscher, Rainer, Habbig, Sandra, Möller, Kristina, Kirchner, Marietta, Schaefer, Franz, Schmitt, Claus Peter, Querfeld, Uwe
Publicado 2019

Modeling of ACTN4-Based Podocytopathy Using Drosophila Nephrocytes

por Odenthal, Johanna, Dittrich, Sebastian, Ludwig, Vivian, Merz, Tim, Reitmeier, Katrin, Reusch, Björn, Höhne, Martin, Cosgun, Zülfü C., Hohenadel, Maximilian, Putnik, Jovana, Göbel, Heike, Rinschen, Markus M., Altmüller, Janine, Koehler, Sybille, Schermer, Bernhard, Benzing, Thomas, Beck, Bodo B., Brinkkötter, Paul T., Habbig, Sandra, Bartram, Malte P.
Publicado 2022

Low renal but high extrarenal phenotype variability in Schimke immuno-osseous dysplasia

por Lipska-Ziętkiewicz, Beata S., Gellermann, Jutta, Boyer, Olivia, Gribouval, Olivier, Ziętkiewicz, Szymon, Kari, Jameela A., Shalaby, Mohamed A., Ozaltin, Fatih, Dusek, Jiri, Melk, Anette, Bayazit, Aysun K., Massella, Laura, Hyla-Klekot, Lidia, Habbig, Sandra, Godron, Astrid, Szczepańska, Maria, Bieniaś, Beata, Drożdż, Dorota, Odeh, Rasha, Jarmużek, Wioletta, Zachwieja, Katarzyna, Trautmann, Agnes, Antignac, Corinne, Schaefer, Franz
Publicado 2017

Targeted deletion of the AAA-ATPase Ruvbl1 in mice disrupts ciliary integrity and causes renal disease and hydrocephalus

por Dafinger, Claudia, Rinschen, Markus M., Borgal, Lori, Ehrenberg, Carolin, Basten, Sander G., Franke, Mareike, Höhne, Martin, Rauh, Manfred, Göbel, Heike, Bloch, Wilhelm, Wunderlich, F. Thomas, Peters, Dorien J. M., Tasche, Dirk, Mishra, Tripti, Habbig, Sandra, Dötsch, Jörg, Müller, Roman-Ulrich, Brüning, Jens C., Persigehl, Thorsten, Giles, Rachel H., Benzing, Thomas, Schermer, Bernhard, Liebau, Max C.
Publicado 2018

Germline C1GALT1C1 mutation causes a multisystem chaperonopathy

por Erger, Florian, Aryal, Rajindra P., Reusch, Björn, Matsumoto, Yasuyuki, Meyer, Robert, Zeng, Junwei, Knopp, Cordula, Noel, Maxence, Muerner, Lukas, Wenzel, Andrea, Kohl, Stefan, Tschernoster, Nikolai, Rappl, Gunter, Rouvet, Isabelle, Schröder-Braunstein, Jutta, Seibert, Felix S., Thiele, Holger, Häusler, Martin G., Weber, Lutz T., Büttner-Herold, Maike, Elbracht, Miriam, Cummings, Sandra F., Altmüller, Janine, Habbig, Sandra, Cummings, Richard D., Beck, Bodo B.
Publicado 2023