Torthaí cuardaigh - Bergmann, Carsten

Educational paper: Ciliopathies de réir Bergmann, Carsten

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ARPKD and early manifestations of ADPKD: the original polycystic kidney disease and phenocopies de réir Bergmann, Carsten

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Genetics of Autosomal Recessive Polycystic Kidney Disease and Its Differential Diagnoses de réir Bergmann, Carsten

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Response to “Nephronophthisis Is an Important Differential Diagnosis of Nonspecific Interstitial Nephritis in Adults” de réir Choi, Mira, Bergmann, Carsten

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Transcriptional Complexity in Autosomal Recessive Polycystic Kidney Disease de réir Frank, Valeska, Zerres, Klaus, Bergmann, Carsten

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Clinical utility gene card for: Meckel syndrome – update 2016 de réir Bergmann, Carsten, Frank, Valeska, Salonen, Riitta

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The wind of change in the management of autosomal dominant polycystic kidney disease in childhood de réir Gimpel, Charlotte, Bergmann, Carsten, Mekahli, Djalila

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Correction to: The wind of change in the management of autosomal dominant polycystic kidney disease in childhood de réir Gimpel, Charlotte, Bergmann, Carsten, Mekahli, Djalila

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Retrospective genetic analysis illustrates the spectrum of autosomal Alport syndrome in a case of living-related donor kidney transplantation de réir Petzold, Friederike, Bachmann, Anette, Bergmann, Carsten, Helmchen, Udo, Halbritter, Jan

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Diagnosing FSGS without kidney biopsy – a novel INF2-mutation in a family with ESRD of unknown origin de réir Münch, Johannes, Grohmann, Maik, Lindner, Tom H., Bergmann, Carsten, Halbritter, Jan

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Long-term follow-up of retinal function and structure in TRPM1-associated complete congenital stationary night blindness de réir Al-Hujaili, Haneen, Taskintuna, Ibrahim, Neuhaus, Christine, Bergmann, Carsten, Schatz, Patrik

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Deleterious Impact of a Novel CFH Splice Site Variant in Atypical Hemolytic Uremic Syndrome de réir Schönauer, Ria, Seidel, Anna, Grohmann, Maik, Lindner, Tom H., Bergmann, Carsten, Halbritter, Jan

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Tectonic gene mutations in patients with Joubert syndrome de réir Huppke, Peter, Wegener, Eike, Böhrer-Rabel, Helena, Bolz, Hanno J, Zoll, Barbara, Gärtner, Jutta, Bergmann, Carsten

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Effective immunosuppressive management with belatacept and eculizumab in post-transplant aHUS due to a homozygous deletion of CFHR1/CFHR3 and the presence of CFH antibodies de réir Münch, Johannes, Bachmann, Anette, Grohmann, Maik, Mayer, Christof, Kirschfink, Michael, Lindner, Tom H, Bergmann, Carsten, Halbritter, Jan

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Treating C3 glomerulopathy with eculizumab de réir Welte, Thomas, Arnold, Frederic, Kappes, Julia, Seidl, Maximilian, Häffner, Karsten, Bergmann, Carsten, Walz, Gerd, Neumann-Haefelin, Elke

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Polycystic kidney disease de réir Bergmann, Carsten, Guay-Woodford, Lisa M., Harris, Peter C., Horie, Shigeo, Peters, Dorien J. M., Torres, Vicente E.

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Defective claudin-10 causes a novel variation of HELIX syndrome through compromised tight junction strand assembly de réir Sewerin, Sebastian, Piontek, Jörg, Schönauer, Ria, Grunewald, Sonja, Rauch, Angelika, Neuber, Steffen, Bergmann, Carsten, Günzel, Dorothee, Halbritter, Jan

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Interstitial Nephritis: A Change in Diagnosis With Next-Generation Sequencing de réir Choi, Mira, Rübsam, Anne, Schulz, Marten, Decker, Eva, Friedrich, Anja, Schrezenmeier, Eva, Halleck, Fabian, Eckardt, Kai-Uwe, Bergmann, Carsten

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Eculizumab in chemotherapy-induced thrombotic microangiopathy de réir Schulte-Kemna, Lena, Reister, Barbara, Bettac, Lucas, Ludwig, Ulla, Fürst, Daniel, Mytilineos, Joannis, Bergmann, Carsten, van Erp, Rene, Schröppel, Bernd

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Charcot‐Marie‐Tooth Neuropathy Type 2 and P0 Point Mutations: Two Novel Amino Acid Substitutions (Asp61Gly; Tyr119Cys) and a Possible “Hotspot” on Thr124Met de réir Senderek, Jan, Hermanns, Benita, Lehmann, Ute, Bergmann, Carsten, Marx, Georg, Kabus, Christian, Timmerman, Vincent, Stoltenburg‐Didinger, Gisela, Schröder, J. Michael

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