ICD-11: an international classification of diseases for the twenty-first century von Harrison, James E, Weber, Stefanie, Jakob, Robert, Chute, Christopher G

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Protective effects of rituximab on puromycin-induced apoptosis, loss of adhesion and cytoskeletal alterations in human podocytes von Jeruschke, Stefanie, Alex, Dana, Hoyer, Peter Friedrich, Weber, Stefanie

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Die Auswirkungen von Primärdatenqualität und -interoperabilität auf Analysen von Real-World-Daten von Weber, Stefanie

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Resolution of inflammation by interleukin-9-producing type 2 innate lymphoid cells von Rauber, Simon, Luber, Markus, Weber, Stefanie, Maul, Lisa, Soare, Alina, Wohlfahrt, Thomas, Lin, Neng-Yu, Dietel, Katharina, Bozec, Aline, Herrmann, Martin, Kaplan, Mark H, Weigmann, Benno, Zaiss, Mario M, Fearon, Ursula, Veale, Douglas J, Cañete, Juan D, Distler, Oliver, Rivellese, Felice, Pitzalis, Costantino, Neurath, Markus F, McKenzie, Andrew N J, Wirtz, Stefan, Schett, Georg, Distler, Jörg H W, Ramming, Andreas

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Autosomal dominant tubulointerstitial kidney disease von Devuyst, Olivier, Olinger, Eric, Weber, Stefanie, Eckardt, Kai-Uwe, Kmoch, Stanislav, Rampoldi, Luca, Bleyer, Anthony J.

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Synthesis and Bioactivity of a Macrocidin B Stereoisomer von Weber, Stefanie E, Gaß, Juliane, Zeng, Haoxuan, Erb-Brinkmann, Maike, Schobert, Rainer

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SARS‐CoV‐2 worldwide replication drives rapid rise and selection of mutations across the viral genome: a time‐course study – potential challenge for vaccines and therapies von Weber, Stefanie, Ramirez, Christina M, Weiser, Barbara, Burger, Harold, Doerfler, Walter

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

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Cutting Edge: Homeostasis of Innate Lymphoid Cells Is Imbalanced in Psoriatic Arthritis von Soare, Alina, Weber, Stefanie, Maul, Lisa, Rauber, Simon, Gheorghiu, Ana Maria, Luber, Markus, Houssni, Ismail, Kleyer, Arnd, von Pickardt, Gero, Gado, Manuel, Simon, David, Rech, Jürgen, Schett, Georg, Distler, Jörg H W, Ramming, Andreas

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International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people von Gimpel, Charlotte, Bergmann, Carsten, Bockenhauer, Detlef, Breysem, Luc, Cadnapaphornchai, Melissa A., Cetiner, Metin, Dudley, Jan, Emma, Francesco, Konrad, Martin, Harris, Tess, Harris, Peter C., König, Jens, Liebau, Max C., Marlais, Matko, Mekahli, Djalila, Metcalfe, Alison M., Oh, Jun, Perrone, Ronald D., Sinha, Manish D., Titieni, Andrea, Torra, Roser, Weber, Stefanie, Winyard, Paul J. D., Schaefer, Franz

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Inheritable epigenetic response towards foreign DNA entry by mammalian host cells: a guardian of genomic stability von Doerfler, Walter, Weber, Stefanie, Naumann, Anja

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Trans-[bis(benzimidazol-2-ylidene)dichlorido]platinum(II) complexes with peculiar modes of action and activity against cisplatin-resistant cancer cells von Bär, Sofia I., Schleser, Sebastian W., Oberhuber, Natalie, Herrmann, Alexander, Schlotte, Luca, Weber, Stefanie E., Schobert, Rainer

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A Distinct DNA-Methylation Boundary in the 5′- Upstream Sequence of the FMR1 Promoter Binds Nuclear Proteins and Is Lost in Fragile X Syndrome von Naumann, Anja, Hochstein, Norbert, Weber, Stefanie, Fanning, Ellen, Doerfler, Walter

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Ubiquitous Micro-Modular Homologies among Genomes from Viruses to Bacteria to Human Mitochondrial DNA: Platforms for Recombination during Evolution? von Weber, Stefanie, Ramirez, Christina M, Doerfler, Walter

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Bartter's and Gitelman's syndrome von Seyberth, Hannsjörg W, Weber, Stefanie, Kömhoff, Martin

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Case report: Febrile infection-related epilepsy syndrome in a 14-year-old girl with multiple organ failure and lethal outcome von Ruttkowski, Lars, Wallot, Ines, Korell, Marie, Daur, Elke, Seipelt, Peter, Leonhardt, Andreas, Weber, Stefanie, Mand, Nadine

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The impact of primary data quality and interoperability on the analysis of real-world data von Weber, Stefanie

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Coding undiagnosed rare disease patients in health information systems: recommendations from the RD-CODE project von Angin, Céline, Mazzucato, Monica, Weber, Stefanie, Kirch, Kurt, Abdel Khalek, Waed, Ali, Houda, Maiella, Sylvie, Olry, Annie, Jannot, Anne-Sophie, Rath, Ana

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Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes von Büscher, Rainer, Büscher, Anja K., Weber, Stefanie, Mohr, Julia, Hegen, Bianca, Vester, Udo, Hoyer, Peter F.

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