Search Results - Liebau, Max C

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  1. 1
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    Risks and benefits of ChatGPT in informing patients and families with rare kidney diseases: an explorative assessment by the European Rare Kidney Disease Reference Network (ERKNet) by Eerde, Albertien van (Author) , Teixeira, Ana (Author) , Galletti, Flavia (Author) , Maternik, Michal (Author) , Capone, Valentina (Author) , Westland, Rik (Author) , Mulder, Jaap (Author) , Halbritter, Jan (Author) , Osterholt, Thomas (Author) , Neukel, Valentina (Author) , Weber, Lutz T. (Author) , Liebau, Max C. (Author) , Schaefer, Franz (Author) , Kohl, Stefan (Author) ,


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  2. 2
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    Urinary Dickkopf-related protein 3 as a novel biomarker for kidney function decline in children with Alport syndrome by Böckhaus, Jan Simon (Author) , Tönshoff, Burkhard (Author) , Weber, Lutz T. (Author) , Pape, Lars (Author) , Latta, Kay (Author) , Fehrenbach, Henry (Author) , Lange-Sperandio, Baerbel (Author) , Kettwig, Matthias (Author) , König, Sabine (Author) , John-Kroegel, Ulrike (Author) , Gellermann, Jutta (Author) , Galiano, Matthias (Author) , Jami, Sima (Author) , Pieper, Dennis (Author) , Dihazi, Gry Helene (Author) , Hafke, Angelika (Author) , Kohl, Stefan (Author) , Liebau, Max C. (Author) , König, Jens (Author) , Haffner, Dieter (Author) , Gross, Oliver (Author) , Wallbach, Manuel (Author) ,


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  3. 3
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    Urinary peptide signature distinguishes autosomal recessive polycystic kidney disease from other causes of chronic kidney disease by Burgmaier, Kathrin (Author) , Buffin-Meyer, Bénédicte (Author) , Klein, Julie (Author) , Becknell, Brian (Author) , McLeod, Daryl (Author) , Boeckhaus, Jan (Author) , Gross, Oliver (Author) , Dafinger, Claudia (Author) , Siwy, Justyna (Author) , Decramer, Stéphane (Author) , Schaefer, Franz (Author) , Liebau, Max C (Author) , Schanstra, Joost P (Author) ,


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  4. 4
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    Renal and extrarenal phenotypes in patients with HNF1B variants and chromosome 17q12 microdeletions by Buffin-Meyer, Bénédicte (Author) , Richard, Juliette (Author) , Guigonis, Vincent (Author) , Weber, Stefanie (Author) , König, Jens (Author) , Heidet, Laurence (Author) , Moussaoui, Nabila (Author) , Vu, Jeanne-Pierrette (Author) , Faguer, Stanislas (Author) , Casemayou, Audrey (Author) , Prakash, Richa (Author) , Baudouin, Véronique (Author) , Hogan, Julien (Author) , Alexandrou, Demi (Author) , Bockenhauer, Detlef (Author) , Bacchetta, Justine (Author) , Ranchin, Bruno (Author) , Pruhova, Stepanka (Author) , Zieg, Jakub (Author) , Lahoche, Annie (Author) , Okorn, Christine (Author) , Antal-Kónya, Violetta (Author) , Morin, Denis (Author) , Becherucci, Francesca (Author) , Habbig, Sandra (Author) , Liebau, Max C. (Author) , Mauras, Mathilde (Author) , Nijenhuis, Tom (Author) , Llanas, Brigitte (Author) , Mekahli, Djalila (Author) , Thumfart, Julia (Author) , Tönshoff, Burkhard (Author) , Massella, Laura (Author) , Eckart, Philippe (Author) , Cloarec, Sylvie (Author) , Cruz, Alejandro (Author) , Patzer, Ludwig (Author) , Roussey, Gwenaelle (Author) , Vrillon, Isabelle (Author) , Dunand, Olivier (Author) , Bessenay, Lucie (Author) , Taroni, Francesca (Author) , Zaniew, Marcin (Author) , Louillet, Ferielle (Author) , Bergmann, Carsten (Author) , Schaefer, Franz (Author) , van Eerde, Albertien M. (Author) , Schanstra, Joost P. (Author) , Decramer, Stéphane (Author) , Ariceta, Gema (Author) , Benetti, Elisa (Author) , Benz, Marcus R. (Author) , Bjerre, Anna (Author) , Boudailliez, Bernard R. (Author) , Bouts, Antonia (Author) , Drube, Jens (Author) , Gjerstad, Ann Christin (Author) , Jankauskiene, Augustina (Author) , Jávorszky, Eszter (Author) , Jay, Nadine (Author) , Kirschstein, Martin (Author) , Varda, Nataša Marčun (Author) , Niel, Olivier (Author) , Nobili, François (Author) , Pietrement, Christine (Author) , Ruzgiene, Dovile (Author) , Schild, Raphael (Author) , Staude, Hagen (Author) , Tory, Kálmán (Author) , Tsimaratos, Michel (Author) , Walden, Ulrike (Author) , Zappel, Hildegard (Author) ,


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  5. 5
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    Design of two ongoing clinical trials of tolvaptan in the treatment of pediatric patients with autosomal recessive polycystic kidney disease by Mekahli, Djalila (Author) , Liebau, Max C. (Author) , Cadnapaphornchai, Melissa A. (Author) , Goldstein, Stuart L. (Author) , Greenbaum, Larry (Author) , Litwin, Mieczysław (Author) , Seeman, Tomas (Author) , Schaefer, Franz (Author) , Guay-Woodford, Lisa M. (Author) ,


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  6. 6
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    Implications of early diagnosis of autosomal dominant polycystic kidney disease: a post hoc analysis of the TEMPO 3:4 trial by Janssens, Peter (Author) , Jouret, François (Author) , Bammens, Bert (Author) , Liebau, Max C. (Author) , Schaefer, Franz (Author) , Dandurand, Ann (Author) , Perrone, Ronald D. (Author) , Müller, Roman-Ulrich (Author) , Pao, Christina S. (Author) , Mekahli, Djalila (Author) ,


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  7. 7
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    Gastrostomy tube insertion in pediatric patients with autosomal recessive polycystic kidney disease (ARPKD): current practice by Burgmaier, Kathrin (Author) , Brandt, Joy (Author) , Shroff, Rukshana (Author) , Witters, Peter (Author) , Weber, Lutz T. (Author) , Dötsch, Jörg (Author) , Schaefer, Franz (Author) , Mekahli, Djalila (Author) , Liebau, Max C. (Author) ,


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  8. 8
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    Protection of human podocytes from Shiga toxin 2-induced phosphorylation of mitogen-activated protein kinases and apoptosis by human serum amyloid P component by Dettmar, Anne K. (Author) , Binder, Elisabeth (Author) , Greiner, Friederike R. (Author) , Liebau, Max C. (Author) , Kurschat, Christine E. (Author) , Jungraithmayr, Therese C. (Author) , Saleem, Moin A. (Author) , Schmitt, Claus P. (Author) , Feifel, Elisabeth (Author) , Orth-Höller, Dorothea (Author) , Kemper, Markus J. (Author) , Pepys, Mark (Author) , Würzner, Reinhard (Author) , Oh, Jun (Author) ,


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