Update on Hereditary Kidney Stone Disease and Introduction of a New Clinical Patient Registry in Germany by Jan Halbritter, Anna Seidel, Luise Müller, Ria Schönauer, Bernd Hoppe

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Challenging Disease Ontology by Instances of Atypical PKHD1 and PKD1 Genetics by Jonathan de Fallois, Ria Schönauer, Johannes Münch, Mato Nagel, Bernt Popp, Jan Halbritter

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Delta weight loss unlike genetic variation associates with hyperoxaluria after malabsorptive bariatric surgery by Lotte Scherer, Ria Schönauer, Melanie Nemitz-Kliemchen, Tobias Hagemann, Elena Hantmann, Jonathan de Fallois, Friederike Petzold, Matthias Blüher, Jan Halbritter

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Modelling polycystic liver disease progression using age-adjusted liver volumes and targeted mutational analysis by Dana Sierks, Ria Schönauer, Anja Friedrich, Elena Hantmann, Jonathan de Fallois, Nikolas Linder, Janett Fischer, Adam Herber, Carsten Bergmann, Thomas Berg, Jan Halbritter

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Novel Mutations in the Asparagine Synthetase Gene (ASNS) Associated With Microcephaly by Dorit Schleinitz, Anna Seidel, Ruth Stassart, Jürgen Klammt, Petra G. Hirrlinger, Ulrike Winkler, Susanne Köhler, John T. Heiker, John T. Heiker, Ria Schönauer, Joanna Bialek, Knut Krohn, Katrin Hoffmann, Peter Kovacs, Johannes Hirrlinger, Johannes Hirrlinger

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