First reported nosocomial outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in a pediatric dialysis unit
Schwierzeck, Vera, König, Jens Christian, Kühn, Joachim, Mellmann, Alexander, Correa-Martínez, Carlos Luis, Omran, Heymut, Konrad, Martin, Kaiser, Thomas, Kampmeier, Stefanie
Published in Clinical infectious diseases (15.01.2021)
Published in Clinical infectious diseases (15.01.2021)
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Phenotypic Spectrum of Children with Nephronophthisis and Related Ciliopathies
König, Jens, Kranz, Birgitta, König, Sabine, Schlingmann, Karl Peter, Titieni, Andrea, Tönshoff, Burkhard, Habbig, Sandra, Pape, Lars, Häffner, Karsten, Hansen, Matthias, Büscher, Anja, Bald, Martin, Billing, Heiko, Schild, Raphael, Walden, Ulrike, Hampel, Tobias, Staude, Hagen, Riedl, Magdalena, Gretz, Norbert, Lablans, Martin, Bergmann, Carsten, Hildebrandt, Friedhelm, Omran, Heymut, Konrad, Martin
Published in Clinical journal of the American Society of Nephrology (07.12.2017)
Published in Clinical journal of the American Society of Nephrology (07.12.2017)
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A multicenter, randomized, placebo-controlled, double-blind phase 3 trial with open-arm comparison indicates safety and efficacy of nephroprotective therapy with ramipril in children with Alport’s syndrome
Gross, Oliver, Tönshoff, Burkhard, Weber, Lutz T., Pape, Lars, Latta, Kay, Fehrenbach, Henry, Lange-Sperandio, Baerbel, Zappel, Hildegard, Hoyer, Peter, Staude, Hagen, König, Sabine, John, Ulrike, Gellermann, Jutta, Hoppe, Bernd, Galiano, Matthias, Hoecker, Britta, Ehren, Rasmus, Lerch, Christian, Kashtan, Clifford E., Harden, Markus, Boeckhaus, Jan, Friede, Tim, Koziolek, Michael, Bramlage, Carsten Paul, Weber, Frauke, Albrecht-Nock, Tanja, Sonntag, Joseph, Frese, Jenny, Kettwig, Matthias, Hilgers, Reinhard, Hansen, Matthias, Wedekin, Mirja, Meyer, Nicole, Klaiber, Susanne, Gessner, Michaela, Liebau, Max, Vogt-Weigeldt, Anne-Kristin, Jungraithmayr, Therese, Ponsel, Sabine, Jacoby, Ulrike, Konrad, Martin, Kranz, Brigitta, Koenig, Jens, Loechtermann, Lisa, Pohl, Michael, Husain, Ralf, Mueller, Katrin, Thumfart, Julia, Schalk, Gesa, Feldkoetter, Markus, Schmidt, Sabine, Sauerstein, Katja, Muschiol, Evelin, Billing, Heiko, Wilkening, Frauke
Published in Kidney international (01.06.2020)
Published in Kidney international (01.06.2020)
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Germline De Novo Mutations in ATP1A1 Cause Renal Hypomagnesemia, Refractory Seizures, and Intellectual Disability
Schlingmann, Karl P., Bandulik, Sascha, Mammen, Cherry, Tarailo-Graovac, Maja, Holm, Rikke, Baumann, Matthias, König, Jens, Lee, Jessica J.Y., Drögemöller, Britt, Imminger, Katrin, Beck, Bodo B., Altmüller, Janine, Thiele, Holger, Waldegger, Siegfried, van’t Hoff, William, Kleta, Robert, Warth, Richard, van Karnebeek, Clara D.M., Vilsen, Bente, Bockenhauer, Detlef, Konrad, Martin
Published in American journal of human genetics (01.11.2018)
Published in American journal of human genetics (01.11.2018)
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Imaging of Kidney Cysts and Cystic Kidney Diseases in Children: An International Working Group Consensus Statement
Gimpel, Charlotte, Avni, E Fred, Breysem, Luc, Burgmaier, Kathrin, Caroli, Anna, Cetiner, Metin, Haffner, Dieter, Hartung, Erum A, Franke, Doris, König, Jens, Liebau, Max C, Mekahli, Djalila, Ong, Albert C M, Pape, Lars, Titieni, Andrea, Torra, Roser, Winyard, Paul J D, Schaefer, Franz
Published in Radiology (01.03.2019)
Published in Radiology (01.03.2019)
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Progressive liver, kidney, and heart degeneration in children and adults affected by TULP3 mutations
Devane, John, Ott, Elisabeth, Olinger, Eric G., Epting, Daniel, Decker, Eva, Friedrich, Anja, Bachmann, Nadine, Renschler, Gina, Eisenberger, Tobias, Briem-Richter, Andrea, Grabhorn, Enke Freya, Powell, Laura, Wilson, Ian J., Rice, Sarah J., Miles, Colin G., Wood, Katrina, Trivedi, Palak, Hirschfield, Gideon, Pietrobattista, Andrea, Wohler, Elizabeth, Mezina, Anya, Sobreira, Nara, Agolini, Emanuele, Maggiore, Giuseppe, Dahmer-Heath, Mareike, Yilmaz, Ali, Boerries, Melanie, Metzger, Patrick, Schell, Christoph, Grünewald, Inga, Konrad, Martin, König, Jens, Schlevogt, Bernhard, Sayer, John A., Bergmann, Carsten
Published in American journal of human genetics (05.05.2022)
Published in American journal of human genetics (05.05.2022)
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International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people
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
Published in Nature reviews. Nephrology (01.11.2019)
Published in Nature reviews. Nephrology (01.11.2019)
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Conference Proceeding
mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy
Schlingmann, Karl P, Jouret, François, Shen, Kuang, Nigam, Anukrati, Arjona, Francisco J, Dafinger, Claudia, Houillier, Pascal, Jones, Deborah P, Kleinerüschkamp, Felix, Oh, Jun, Godefroid, Nathalie, Eltan, Mehmet, Güran, Tülay, Burtey, Stéphane, Parotte, Marie-Christine, König, Jens, Braun, Alina, Bos, Caro, Ibars Serra, Maria, Rehmann, Holger, Zwartkruis, Fried J T, Renkema, Kirsten Y, Klingel, Karin, Schulze-Bahr, Eric, Schermer, Bernhard, Bergmann, Carsten, Altmüller, Janine, Thiele, Holger, Beck, Bodo B, Dahan, Karin, Sabatini, David, Liebau, Max C, Vargas-Poussou, Rosa, Knoers, Nine V A M, Konrad, Martin, de Baaij, Jeroen H F
Published in Journal of the American Society of Nephrology (01.11.2021)
Published in Journal of the American Society of Nephrology (01.11.2021)
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Immunofluorescence analyses of respiratory epithelial cells aid the diagnosis of nephronophthisis
Hellmann, Carlotta, Wohlgemuth, Kai, Pennekamp, Petra, George, Sebastian, Dahmer-Heath, Mareike, Konrad, Martin, Omran, Heymut, König, Jens
Published in Pediatric nephrology (Berlin, West) (05.08.2024)
Published in Pediatric nephrology (Berlin, West) (05.08.2024)
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NPHP1 gene-associated nephronophthisis is associated with an occult retinopathy
Birtel, Johannes, Spital, Georg, Book, Marius, Habbig, Sandra, Bäumner, Sören, Riehmer, Vera, Beck, Bodo B., Rosenkranz, David, Bolz, Hanno J., Dahmer-Heath, Mareike, Herrmann, Philipp, König, Jens, Charbel Issa, Peter
Published in Kidney international (01.11.2021)
Published in Kidney international (01.11.2021)
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HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry
Okorn, Christine, Goertz, Anne, Vester, Udo, Beck, Bodo B., Bergmann, Carsten, Habbig, Sandra, König, Jens, Konrad, Martin, Müller, Dominik, Oh, Jun, Ortiz-Brüchle, Nadina, Patzer, Ludwig, Schild, Raphael, Seeman, Tomas, Staude, Hagen, Thumfart, Julia, Tönshoff, Burkhard, Walden, Ulrike, Weber, Lutz, Zaniew, Marcin, Zappel, Hildegard, Hoyer, Peter F., Weber, Stefanie
Published in Pediatric nephrology (Berlin, West) (01.06.2019)
Published in Pediatric nephrology (Berlin, West) (01.06.2019)
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Bardet-Biedl syndrome improved diagnosis criteria and management: Inter European Reference Networks consensus statement and recommendations
Dollfus, Hélène, Lilien, Marc R, Maffei, Pietro, Verloes, Alain, Muller, Jean, Bacci, Giacomo M, Cetiner, Metin, van den Akker, Erica L T, Grudzinska Pechhacker, Monika, Testa, Francesco, Lacombe, Didier, Stokman, Marijn F, Simonelli, Francesca, Gouronc, Aurélie, Gavard, Amélie, van Haelst, Mieke M, Koenig, Jens, Rossignol, Sylvie, Bergmann, Carsten, Zacchia, Miriam, Leroy, Bart P, Mosbah, Héléna, Van Eerde, Albertien M, Mekahli, Djalila, Servais, Aude, Poitou, Christine, Valverde, Diana
Published in European journal of human genetics : EJHG (31.07.2024)
Published in European journal of human genetics : EJHG (31.07.2024)
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Emulation of the control cohort of a randomized controlled trial in pediatric kidney transplantation with Real-World Data from the CERTAIN Registry
Patry, Christian, Sauer, Lukas D., Sander, Anja, Krupka, Kai, Fichtner, Alexander, Brezinski, Jolanda, Geissbühler, Yvonne, Aubrun, Elodie, Grinienko, Anna, Strologo, Luca Dello, Haffner, Dieter, Oh, Jun, Grenda, Ryszard, Pape, Lars, Topaloğlu, Rezan, Weber, Lutz T., Bouts, Antonia, Kim, Jon Jin, Prytula, Agnieszka, König, Jens, Shenoy, Mohan, Höcker, Britta, Tönshoff, Burkhard
Published in Pediatric nephrology (Berlin, West) (01.05.2023)
Published in Pediatric nephrology (Berlin, West) (01.05.2023)
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Development of a tool for predicting HNF1B mutations in children and young adults with congenital anomalies of the kidneys and urinary tract
Kołbuc, Marcin, Kołek, Mateusz F., Motyka, Rafał, Bieniaś, Beata, Habbig, Sandra, Burgmaier, Kathrin, Prikhodina, Larisa, Papizh, Svetlana, Tasic, Velibor, Okorn, Christine, Szczepańska, Maria, Kiliś-Pstrusińska, Katarzyna, Wasilewska, Anna, Adamczyk, Piotr, Tkaczyk, Marcin, Pańczyk-Tomaszewska, Małgorzata, Miklaszewska, Monika, Pawlaczyk, Krzysztof, Bukowska-Olech, Ewelina, Jamsheer, Aleksander, Jankauskiene, Augustina, König, Jens, Cheong, Hae Il, Ahn, Yo Han, Kaspar, Sophie, Sikora, Przemysław, Beck, Bodo B., Zaniew, Marcin
Published in Pediatric nephrology (Berlin, West) (01.06.2024)
Published in Pediatric nephrology (Berlin, West) (01.06.2024)
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Improved Care and Treatment Options for Patients with Hyperphagia-Associated Obesity in Bardet-Biedl Syndrome
Cetiner, Metin, Bergmann, Carsten, Bettendorf, Markus, Faust, Johanna, Gäckler, Anja, Gillissen, Bernarda, Hansen, Matthias, Kerber, Maximilian, Klaus, Günter, König, Jens, Kühlewein, Laura, Oh, Jun, Richter-Unruh, Annette, von Schnurbein, Julia, Wabitsch, Martin, Weihrauch-Blüher, Susann, Pape, Lars
Published in Klinische Padiatrie (01.09.2024)
Published in Klinische Padiatrie (01.09.2024)
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Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum
Matejas, Verena, Hinkes, Bernward, Alkandari, Faisal, Al-Gazali, Lihadh, Annexstad, Ellen, Aytac, Mehmet B., Barrow, Margaret, Bláhová, Květa, Bockenhauer, Detlef, Cheong, Hae Il, Maruniak-Chudek, Iwona, Cochat, Pierre, Dötsch, Jörg, Gajjar, Priya, Hennekam, Raoul C., Janssen, Françoise, Kagan, Mikhail, Kariminejad, Ariana, Kemper, Markus J., Koenig, Jens, Kogan, Jillene, Kroes, Hester Y., Kuwertz-Bröking, Eberhard, Lewanda, Amy F., Medeira, Ana, Muscheites, Jutta, Niaudet, Patrick, Pierson, Michel, Saggar, Anand, Seaver, Laurie, Suri, Mohnish, Tsygin, Alexey, Wühl, Elke, Zurowska, Aleksandra, Uebe, Steffen, Hildebrandt, Friedhelm, Antignac, Corinne, Zenker, Martin
Published in Human mutation (01.09.2010)
Published in Human mutation (01.09.2010)
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Molecular HLA mismatching for prediction of primary humoral alloimmunity and graft function deterioration in paediatric kidney transplantation
Kim, Jon Jin, Fichtner, Alexander, Copley, Hannah C, Gragert, Loren, Süsal, Caner, Dello Strologo, Luca, Oh, Jun, Pape, Lars, Weber, Lutz T, Weitz, Marcus, König, Jens, Krupka, Kai, Tönshoff, Burkhard, Kosmoliaptsis, Vasilis
Published in Frontiers in immunology (15.03.2023)
Published in Frontiers in immunology (15.03.2023)
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Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease
Burgmaier, Kathrin, Kunzmann, Kevin, Bergmann, Carsten, Buescher, Anja Katrin, Burgmaier, Mathias, Dursun, Ismail, Eid, Loai, Feldkoetter, Markus, Galiano, Matthias, Geßner, Michaela, Goebel, Heike, Hooman, Nakysa, Jankauskiene, Augustina, Klaus, Guenter, König, Jens, Massella, Laura, Mekahli, Djalila, Melek, Engin, Mir, Sevgi, Pape, Lars, Prikhodina, Larisa, Ranchin, Bruno, Schild, Raphael, Seeman, Tomas, Sever, Lale, Shroff, Rukshana, Soliman, Neveen A., Stabouli, Stella, Taranta-Janusz, Katarzyna, Testa, Sara, Thumfart, Julia, Topaloglu, Rezan, Weber, Lutz Thorsten, Wicher, Dorota, Wygoda, Simone, Yilmaz, Alev, Zachwieja, Katarzyna, Zagozdzon, Ilona, Ranguelov, Nadejda, Collard, Laure, Lombet, Jacques, Maquet, Julie, Schalk, Gesa, Beck, Bodo B., Benzing, Thomas, Buettner, Reinhard, Grundmann, Franziska, Kurschat, Christine, Benz, Kerstin, Tzschoppe, Anja, Buchholz, Björn, Buescher, Rainer, Häffner, Karsten, Krügel, Jenny, Stock, Johanna, Oh, Jun, Vinke, Tobias, Sander, Anja, Henn, Michael, Derichs, Ute, Jeck, Nikola, Lange-Sperandio, Bärbel, Kusser, Franziska, Benz, Marcus, Schmidt, Silke, Huppertz-Kessler, Christina, Titieni, Andrea, Wurm, Donald, Billing, Heiko, Nabhan, Marwa M., Lara, Luis Enrique, Papachristou, Fotios, Emma, Francesco, Cerkauskiene, Rimante, Azukaitis, Karolis, Wasilewska, Anna, Balasz-Chmielewska, Irena, Miklaszewska, Monika, Tkaczyk, Marcin, Sikora, Przemyslaw, Zaniew, Marcin, Antoniewicz, Jolanta, Lesiak, Justyna, Afonso, Alberto Caldas, Teixeira, Ana, Paripović, Dusan, Peco-Antic, Amira, Papizh, Svetlana, Bayazit, Aysun Karabay, Anarat, Ali, Kavukcu, Salih, Candan, Cengiz, Caliskan, Salim, Canpolat, Nur, Emre, Sevinc, Akinci, Nurver, Conkar, Secil, Poyrazoglu, Hakan M., Dötsch, Jörg, Schaefer, Franz
Published in The Journal of pediatrics (01.08.2018)
Published in The Journal of pediatrics (01.08.2018)
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Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis
Klämbt, Verena, Gimpel, Charlotte, Bald, Martin, Gerken, Christopher, Billing, Heiko, Loos, Sebastian, Hansen, Matthias, König, Jens, Vinke, Tobias, Montoya, Carmen, Lange-Sperandio, Bärbel, Kirschstein, Martin, Hennies, Imke, Pohl, Martin, Häffner, Karsten
Published in Pediatric nephrology (Berlin, West) (01.02.2021)
Published in Pediatric nephrology (Berlin, West) (01.02.2021)
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