Severe Joubert syndrome in family with homozygous POC1B p.Arg106Pro variant is due to a co-inherited deep-intronic mutation in the neighboring CEP290 gene by Christian Betz, Björn Reusch, Thomas Langmann, Sandra Habbig, Bodo B. Beck, Hanno J. Bolz

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Effective Newborn Screening for Type 1 and 3 Primary Hyperoxaluria by Bernd Hoppe, Cristina Martin-Higueras, Lodovica Borghese, Sophie Kaspar, Björn Reusch, Bodo B. Beck, Adam Walli, Ella Janzen, Sebastian Hegert, Nils Janzen, Katharina Hohenfellner

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Challenges and Considerations in Managing Thrombotic Microangiopathy and Disseminated Intravascular Coagulation in Postpartum Hemorrhage by Jessica K. Kaufeld, Ulf Schönermarck, Lucas Kühne, Jan Hinrich Bräsen, Constantin von Kaisenberg, Bodo B. Beck, Florian Erger, Carsten Bergmann, Anke von Bergwelt-Baildon, Paul T. Brinkkötter, Jan Menne, Linus A. Völker

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Erratum to “Features of Postpartum Hemorrhage-Associated Thrombotic Microangiopathy and Role of Short-Term Complement Inhibition” [Kidney International Reports Volume 9, Issue 4, A... by Jessica K. Kaufeld, Lucas Kühne, Ulf Schönermarck, Jan Hinrich Bräsen, Constantin von Kaisenberg, Bodo B. Beck, Florian Erger, Carsten Bergmann, Anke von Bergwelt-Baildon, Paul T. Brinkkötter, Linus A. Völker, Jan Menne

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Features of Postpartum Hemorrhage-Associated Thrombotic Microangiopathy and Role of Short-Term Complement Inhibition by Jessica K. Kaufeld, Lucas Kühne, Ulf Schönermarck, Jan Hinrich Bräsen, Constantin von Kaisenberg, Bodo B. Beck, Florian Erger, Carsten Bergmann, A.N.K.E. von Bergwelt-Baildon, Paul T. Brinkkötter, Linus A. Völker, Jan Menne

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Multicenter Long-Term Real World Data on Treatment With Lumasiran in Patients With Primary Hyperoxaluria Type 1 by Cristina Martin-Higueras, Lodovica Borghese, Armando Torres, Fátima Fraga-Bilbao, Raquel Santana-Estupiñán, Constantinos J. Stefanidis, Kálmán Tory, Adam Walli, Leire Gondra, Caroline Kempf, Michaela Gessner, Sandra Habbig, Lisa Eifler, Claus P. Schmitt, Benjamin Rüdel, Malte P. Bartram, Bodo B. Beck, Bernd Hoppe

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Intrafamilial Disease Heterogeneity in Primary Hyperoxaluria Type 1 by Lisa J. Deesker, Hazal A. Karacoban, Elisabeth L. Metry, Sander F. Garrelfs, Justine Bacchetta, Olivia Boyer, Laure Collard, Arnaud Devresse, Wesley Hayes, Sally-Anne Hulton, Cristina Martin-Higueras, Shabbir H. Moochhala, Thomas J. Neuhaus, Jun Oh, Larisa Prikhodina, Przemyslaw Sikora, Michiel J.S. Oosterveld, Jaap W. Groothoff, Giorgia Mandrile, Bodo B. Beck

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