Is stiripentol truly effective for treating primary hyperoxaluria?

Por Martin-Higueras, Cristina, Feldkötter, Markus, Hoppe, Bernd
Publicado no Clin Kidney J (2020)

Reply to Ogino and Wilson

Por Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Publicado em 2002

Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy

Por Feldkötter, Markus, Schwarzer, Verena, Wirth, Radu, Wienker, Thomas F., Wirth, Brunhilde
Publicado em 2002

Transition structures and timing of transfer from paediatric to adult-based care after kidney transplantation in Germany: a qualitative study

Por Prüfe, Jenny, Dierks, Marie-Luise, Bethe, Dirk, Oldhafer, Martina, Müther, Silvia, Thumfart, Julia, Feldkötter, Markus, Büscher, Anja, Sauerstein, Katja, Hansen, Matthias, Pohl, Martin, Drube, Jens, Thiel, Florian, Rieger, Susanne, John, Ulrike, Taylan, Christina, Dittrich, Katalin, Hollenbach, Sabine, Klaus, Günter, Fehrenbach, Henry, Kranz, Birgitta, Montoya, Carmen, Lange-Sperandio, Bärbel, Ruckenbrod, Bettina, Billing, Heiko, Staude, Hagen, Brunkhorst, Reinhard, Rusai, Krisztina, Pape, Lars, Kreuzer, Martin
Publicado no BMJ Open (2017)

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)

Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction

Por Kolvenbach, Caroline M., Dworschak, Gabriel C., Frese, Sandra, Japp, Anna S., Schuster, Peggy, Wenzlitschke, Nina, Yilmaz, Öznur, Lopes, Filipa M., Pryalukhin, Alexey, Schierbaum, Luca, van der Zanden, Loes F.M., Kause, Franziska, Schneider, Ronen, Taranta-Janusz, Katarzyna, Szczepańska, Maria, Pawlaczyk, Krzysztof, Newman, William G., Beaman, Glenda M., Stuart, Helen M., Cervellione, Raimondo M., Feitz, Wouter F.J., van Rooij, Iris A.L.M., Schreuder, Michiel F., Steffens, Martijn, Weber, Stefanie, Merz, Waltraut M., Feldkötter, Markus, Hoppe, Bernd, Thiele, Holger, Altmüller, Janine, Berg, Christoph, Kristiansen, Glen, Ludwig, Michael, Reutter, Heiko, Woolf, Adrian S., Hildebrandt, Friedhelm, Grote, Phillip, Zaniew, Marcin, Odermatt, Benjamin, Hilger, Alina C.
Publicado no Am J Hum Genet (2019)