Urinary tract infections in children after renal transplantation

Por John, Ulrike, Kemper, Markus J.
Publicado em 2009

Diagnostic examination of the child with urolithiasis or nephrocalcinosis

Por Hoppe, Bernd, Kemper, Markus J.
Publicado em 2008

Pathogenesis, diagnosis and management of hyperkalemia

Por Lehnhardt, Anja, Kemper, Markus J.
Publicado em 2010

Angiotensin‐converting enzyme inhibitor fetopathy: long‐term outcome

Por Laube, Guido F, Kemper, Markus J, Schubiger, Gregor, Neuhaus, Thomas J
Publicado em 2007

Case report - atypical hemolytic uremic syndrome triggered by influenza B

Por Kobbe, Robin, Schild, Raphael, Christner, Martin, Oh, Jun, Loos, Sebastian, Kemper, Markus J.
Publicado no BMC Nephrol (2017)

Human Factor H-Related Protein 2 (CFHR2) Regulates Complement Activation

Por Eberhardt, Hannes U., Buhlmann, Denise, Hortschansky, Peter, Chen, Qian, Böhm, Sascha, Kemper, Markus J., Wallich, Reinhard, Hartmann, Andrea, Hallström, Teresia, Zipfel, Peter F., Skerka, Christine
Publicado em 2013

Effect of the Dialysis Fluid Buffer on Peritoneal Membrane Function in Children

Por Schmitt, Claus Peter, Nau, Barbara, Gemulla, Gita, Bonzel, Klaus E., Hölttä, Tuula, Testa, Sara, Fischbach, Michel, John, Ulrike, Kemper, Markus J., Sander, Anja, Arbeiter, Klaus, Schaefer, Franz
Publicado em 2013

Double homozygous missense mutations in DACH1 and BMP4 in a patient with bilateral cystic renal dysplasia

Por Schild, Raphael, Knüppel, Tanja, Konrad, Martin, Bergmann, Carsten, Trautmann, Agnes, Kemper, Markus J., Wu, Kongming, Yaklichkin, Sergey, Wang, Jing, Pestell, Richard, Müller-Wiefel, Dirk E., Schaefer, Franz, Weber, Stefanie
Publicado em 2013

BIOKID: Randomized controlled trial comparing bicarbonate and lactate buffer in biocompatible peritoneal dialysis solutions in children [ISRCTN81137991]

Por Nau, Barbara, Schmitt, Claus P, Almeida, Margarida, Arbeiter, Klaus, Ardissino, Gianluigi, Bonzel, Klaus E, Edefonti, Alberto, Fischbach, Michel, Haluany, Karin, Misselwitz, Joachim, Kemper, Markus J, Rönnholm, Kai, Wygoda, Simone, Schaefer, Franz
Publicado em 2004

Rapid Response to Cyclosporin A and Favorable Renal Outcome in Nongenetic Versus Genetic Steroid–Resistant Nephrotic Syndrome

Por Büscher, Anja K., Beck, Bodo B., Melk, Anette, Hoefele, Julia, Kranz, Birgitta, Bamborschke, Daniel, Baig, Sabrina, Lange-Sperandio, Bärbel, Jungraithmayr, Theresa, Weber, Lutz T., Kemper, Markus J., Tönshoff, Burkhard, Hoyer, Peter F., Konrad, Martin, Weber, Stefanie
Publicado no Clin J Am Soc Nephrol (2016)

Protection of Human Podocytes from Shiga Toxin 2-Induced Phosphorylation of Mitogen-Activated Protein Kinases and Apoptosis by Human Serum Amyloid P Component

Por Dettmar, Anne K., Binder, Elisabeth, Greiner, Friederike R., Liebau, Max C., Kurschat, Christine E., Jungraithmayr, Therese C., Saleem, Moin A., Schmitt, Claus-Peter, Feifel, Elisabeth, Orth-Höller, Dorothea, Kemper, Markus J., Pepys, Mark, Würzner, Reinhard, Oh, Jun
Publicado em 2014

Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies

Por Beck, Bodo B, Baasner, Anne, Buescher, Anja, Habbig, Sandra, Reintjes, Nadine, Kemper, Markus J, Sikora, Przemyslaw, Mache, Christoph, Pohl, Martin, Stahl, Mirjam, Toenshoff, Burkhard, Pape, Lars, Fehrenbach, Henry, Jacob, Dorrit E, Grohe, Bernd, Wolf, Matthias T, Nürnberg, Gudrun, Yigit, Gökhan, Salido, Eduardo C, Hoppe, Bernd
Publicado em 2013

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1–SIX1–DNA complexes

Por Ruf, Rainer G., Xu, Pin-Xian, Silvius, Derek, Otto, Edgar A., Beekmann, Frank, Muerb, Ulla T., Kumar, Shrawan, Neuhaus, Thomas J., Kemper, Markus J., Raymond, Richard M., Brophy, Patrick D., Berkman, Jennifer, Gattas, Michael, Hyland, Valentine, Ruf, Eva-Maria, Schwartz, Charles, Chang, Eugene H., Smith, Richard J. H., Stratakis, Constantine A., Weil, Dominique, Petit, Christine, Hildebrandt, Friedhelm
Publicado em 2004

A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome

Por Sadowski, Carolin E., Lovric, Svjetlana, Ashraf, Shazia, Pabst, Werner L., Gee, Heon Yung, Kohl, Stefan, Engelmann, Susanne, Vega-Warner, Virginia, Fang, Humphrey, Halbritter, Jan, Somers, Michael J., Tan, Weizhen, Shril, Shirlee, Fessi, Inès, Lifton, Richard P., Bockenhauer, Detlef, El-Desoky, Sherif, Kari, Jameela A., Zenker, Martin, Kemper, Markus J., Mueller, Dominik, Fathy, Hanan M., Soliman, Neveen A., Hildebrandt, Friedhelm
Publicado no J Am Soc Nephrol (2015)

Mutations in nuclear pore genes NUP93, NUP205, and XPO5 cause steroid resistant nephrotic syndrome

Por Braun, Daniela A., Sadowski, Carolin E., Kohl, Stefan, Lovric, Svjetlana, Astrinidis, Susanne A., Pabst, Werner L., Gee, Heon Yung, Ashraf, Shazia, Lawson, Jennifer A., Shril, Shirlee, Airik, Merlin, Tan, Weizhen, Schapiro, David, Rao, Jia, Choi, Won-Il, Hermle, Tobias, Kemper, Markus J., Pohl, Martin, Ozaltin, Fatih, Konrad, Martin, Bogdanovic, Radovan, Büscher, Rainer, Helmchen, Udo, Serdaroglu, Erkin, Lifton, Richard P., Antonin, Wolfram, Hildebrandt, Friedhelm
Publicado no Nat Genet (2016)

Transitional Care and Adherence of Adolescents and Young Adults After Kidney Transplantation in Germany and Austria: A Binational Observatory Census Within the TRANSNephro Trial

Por Kreuzer, Martin, Prüfe, Jenny, Oldhafer, Martina, Bethe, Dirk, Dierks, Marie-Luise, Müther, Silvia, Thumfart, Julia, Hoppe, Bernd, Büscher, Anja, Rascher, Wolfgang, Hansen, Matthias, Pohl, Martin, Kemper, Markus J., Drube, Jens, Rieger, Susanne, John, Ulrike, Taylan, Christina, Dittrich, Katalin, Hollenbach, Sabine, Klaus, Günter, Fehrenbach, Henry, Kranz, Birgitta, Montoya, Carmen, Lange-Sperandio, Bärbel, Ruckenbrodt, Bettina, Billing, Heiko, Staude, Hagen, Heindl-Rusai, Krisztina, Brunkhorst, Reinhard, Pape, Lars
Publicado no Medicine (Baltimore) (2015)

Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

Por Lehnhardt, Anja, Karnatz, Claartje, Ahlenstiel-Grunow, Thurid, Benz, Kerstin, Benz, Marcus R., Budde, Klemens, Büscher, Anja K., Fehr, Thomas, Feldkötter, Markus, Graf, Norbert, Höcker, Britta, Jungraithmayr, Therese, Klaus, Günter, Koehler, Birgit, Konrad, Martin, Kranz, Birgitta, Montoya, Carmen R., Müller, Dominik, Neuhaus, Thomas J., Oh, Jun, Pape, Lars, Pohl, Martin, Royer-Pokora, Brigitte, Querfeld, Uwe, Schneppenheim, Reinhard, Staude, Hagen, Spartà, Giuseppina, Timmermann, Kirsten, Wilkening, Frauke, Wygoda, Simone, Bergmann, Carsten, Kemper, Markus J.
Publicado no Clin J Am Soc Nephrol (2015)

Mutations in the Human Laminin β2 (LAMB2) Gene and the Associated Phenotypic Spectrum

Por Matejas, Verena, Hinkes, Bernward, Alkandari, Faisal, Al-Gazali, Lihadh, Annexstad, Ellen, Aytac, Mehmet B., Barrow, Margaret, Bláhová, Kvĕta, Bockenhauer, Detlef, Cheong, Hae Il, Maruniak-Chudek, Iwona, Cochat, Pierre, Dötsch, Jörg, Gajjar, Priya, Hennekam, Raoul C., Janssen, Françoise, Kagan, Mikhail, Kariminejad, Ariana, Kemper, Markus J., Koenig, Jens, Kogan, Jillene, Kroes, Hester Y., Kuwertz-Bröking, Eberhard, Lewanda, Amy F., Medeira, Ana, Muscheites, Jutta, Niaudet, Patrick, Pierson, Michel, Saggar, Anand, Seaver, Laurie, Suri, Mohnish, Tsygin, Alexey, Wühl, Elke, Zurowska, Aleksandra, Uebe, Steffen, Hildebrandt, Friedhelm, Antignac, Corinne, Zenker, Martin
Publicado em 2010

Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development

Por Vivante, Asaf, Kleppa, Marc-Jens, Schulz, Julian, Kohl, Stefan, Sharma, Amita, Chen, Jing, Shril, Shirlee, Hwang, Daw-Yang, Weiss, Anna-Carina, Kaminski, Michael M., Shukrun, Rachel, Kemper, Markus J., Lehnhardt, Anja, Beetz, Rolf, Sanna-Cherchi, Simone, Verbitsky, Miguel, Gharavi, Ali G., Stuart, Helen M., Feather, Sally A., Goodship, Judith A., Goodship, Timothy H.J., Woolf, Adrian S., Westra, Sjirk J., Doody, Daniel P., Bauer, Stuart B., Lee, Richard S., Adam, Rosalyn M., Lu, Weining, Reutter, Heiko M., Kehinde, Elijah O., Mancini, Erika J., Lifton, Richard P., Tasic, Velibor, Lienkamp, Soeren S., Jüppner, Harald, Kispert, Andreas, Hildebrandt, Friedhelm
Publicado no Am J Hum Genet (2015)