History, epidemiology and regional diversities of urolithiasis von López, Michelle, Hoppe, Bernd

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Nephrocalcinosis and urolithiasis in children von Habbig, Sandra, Beck, Bodo Bernhard, Hoppe, Bernd

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Chronic liver disease and hepatic calcium-oxalate deposition in patients with primary hyperoxaluria type I von Recker, Pia, Beck, Bodo Bernhard, Sikora, Przemyslaw, Göbel, Heike, Kemper, Markus Josef, Nazco, Angel, Martin-Higueras, Cristina, Hoppe, Bernd

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Nephrolithiasis and Nephrocalcinosis in Childhood-Risk Factor-Related Current and Future Treatment Options von Weigert, Alexander, Hoppe, Bernd

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Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy von Gross, Oliver, Licht, Christoph, Anders, Hans J., Hoppe, Bernd, Beck, Bodo, Tönshoff, Burkhard, Höcker, Britta, Wygoda, Simone, Ehrich, Jochen H.H., Pape, Lars, Konrad, Martin, Rascher, Wolfgang, Dötsch, Jörg, Müller-Wiefel, Dirk E., Hoyer, Peter, Knebelmann, Bertrand, Pirson, Yves, Grunfeld, Jean-Pierre, Niaudet, Patrick, Cochat, Pierre, Heidet, Laurence, Lebbah, Said, Torra, Roser, Friede, Tim, Lange, Katharina, Müller, Gerhard A., Weber, Manfred

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Hyperoxaluria Requires TNF Receptors to Initiate Crystal Adhesion and Kidney Stone Disease von Mulay, Shrikant R, Eberhard, Jonathan N, Desai, Jyaysi, Marschner, Julian A, Kumar, Santhosh V R, Weidenbusch, Marc, Grigorescu, Melissa, Lech, Maciej, Eltrich, Nuru, Müller, Lisa, Hans, Wolfgang, Hrabě de Angelis, Martin, Vielhauer, Volker, Hoppe, Bernd, Asplin, John, Burzlaff, Nicolai, Herrmann, Martin, Evan, Andrew, Anders, Hans-Joachim

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Ultrasound-guided percutaneous renal biopsy in 295 children and adolescents: role of ultrasound and analysis of complications von Franke, Mareike, Kramarczyk, Annette, Taylan, Christina, Maintz, David, Hoppe, Bernd, Koerber, Friederike

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Genetic kidney stones disease in adults von Stephan, Rebekka, Hoppe, Bernd

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New Aspects of Kidney Fibrosis-From Mechanisms of Injury to Modulation of Disease von Moeller, Marcus J, Kramann, Rafael, Lammers, Twan, Hoppe, Bernd, Latz, Eicke, Ludwig-Portugall, Isis, Boor, Peter, Floege, Jürgen, Kurts, Christian, Weiskirchen, Ralf, Ostendorf, Tammo

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Kidney stones in primary hyperoxaluria: new lessons learnt von Jacob, Dorrit E, Grohe, Bernd, Geßner, Michaela, Beck, Bodo B, Hoppe, Bernd

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Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome von Zipfel, Peter F, Edey, Matthew, Heinen, Stefan, Józsi, Mihály, Richter, Heiko, Misselwitz, Joachim, Hoppe, Bernd, Routledge, Danny, Strain, Lisa, Hughes, Anne E, Goodship, Judith A, Licht, Christoph, Goodship, Timothy H J, Skerka, Christine

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Hepatic Lactate Dehydrogenase A: An RNA Interference Target for the Treatment of All Known Types of Primary Hyperoxaluria von Ariceta, Gema, Barrios, Kelly, Brown, Bob D., Hoppe, Bernd, Rosskamp, Ralf, Langman, Craig B.

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Urinary citrate excretion in healthy children depends on age and gender von Kirejczyk, Jan K., Porowski, Tadeusz, Konstantynowicz, Jerzy, Kozerska, Agata, Nazarkiewicz, Andrzej, Hoppe, Bernd, Wasilewska, Anna

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Improving Treatment Options for Primary Hyperoxaluria von Hoppe, Bernd, Martin-Higueras, Cristina

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Precise variant interpretation, phenotype ascertainment, and genotype–phenotype correlation of children in the EARLY PRO‐TECT Alport trial von Boeckhaus, Jan, Hoefele, Julia, Riedhammer, Korbinian M., Tönshoff, Burkhard, Ehren, Rasmus, Pape, Lars, Latta, Kay, Fehrenbach, Henry, Lange‐Sperandio, Baerbel, Kettwig, Matthias, Hoyer, Peter, Staude, Hagen, Konrad, Martin, John, Ulrike, Gellermann, Jutta, Hoppe, Bernd, Galiano, Matthias, Gessner, Michaela, Pohl, Michael, Bergmann, Carsten, Friede, Tim, Gross, Oliver

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Dent-2 Disease: A Mild Variant of Lowe Syndrome von Bökenkamp, Arend, MD, PhD, Böckenhauer, Detlef, MD, PhD, Cheong, Hae Il, MD, PhD, Hoppe, Bernd, MD, PhD, Tasic, Velibor, MD, Unwin, Robert, MD, PhD, Ludwig, Michael, PhD

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Long-term outcome after combined or sequential liver and kidney transplantation in children with infantile and juvenile primary hyperoxaluria type 1 von Loos, Sebastian, Kemper, Markus J, Schmaeschke, Kaja, Herden, Uta, Fischer, Lutz, Hoppe, Bernd, Levart, Tanja Kersnik, Grabhorn, Enke, Schild, Raphael, Oh, Jun, Brinkert, Florian

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Plasma oxalate levels in primary hyperoxaluria type I show significant intra-individual variation and do not correlate with kidney function von Hillebrand, Philip, Hoppe, Bernd

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Genetic Risk Factors for Idiopathic Urolithiasis: A Systematic Review of the Literature and Causal Network Analysis von Taguchi, Kazumi, Yasui, Takahiro, Milliner, Dawn Schmautz, Hoppe, Bernd, Chi, Thomas

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Reduction of Plasma Oxalate Levels by Oral Application of Oxalobacter formigenes in 2 Patients With Infantile Oxalosis von Hoppe, Bernd, MD, Dittlich, Katalin, MD, Fehrenbach, Henry, MD, Plum, Georg, PhD, Beck, Bodo B., MD

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