Search Results - Wenzel, Andrea

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  1. 1
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    Germline C1GALT1C1 mutation causes a multisystem chaperonopathy by Erger, Florian (Author) , Aryal, Rajindra P. (Author) , Reusch, Björn (Author) , Matsumoto, Yasuyuki (Author) , Meyer, Robert (Author) , Zeng, Junwei (Author) , Knopp, Cordula (Author) , Noel, Maxence (Author) , Muerner, Lukas (Author) , Wenzel, Andrea (Author) , Kohl, Stefan (Author) , Tschernoster, Nikolai (Author) , Rappl, Gunter (Author) , Rouvet, Isabelle (Author) , Schröder-Braunstein, Jutta (Author) , Seibert, Felix S. (Author) , Thiele, Holger (Author) , Häusler, Martin G. (Author) , Weber, Lutz T. (Author) , Büttner-Herold, Maike (Author) , Elbracht, Miriam (Author) , Cummings, Sandra F. (Author) , Altmüller, Janine (Author) , Habbig, Sandra (Author) , Cummings, Richard D. (Author) , Beck, Bodo B. (Author) ,


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  2. 2
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    MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells by Reusch, Björn (Author) , Bartram, Malte P. (Author) , Dafinger, Claudia (Author) , Palacio-Escat, Nicolàs (Author) , Wenzel, Andrea (Author) , Fenton, Robert A. (Author) , Sáez Rodríguez, Julio (Author) , Schermer, Bernhard (Author) , Benzing, Thomas (Author) , Altmüller, Janine (Author) , Beck, Bodo B. (Author) , Rinschen, Markus M. (Author) ,


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  3. 3
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    Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases by Wopperer, Florian (Author) , Knaup, Karl X. (Author) , Stanzick, Kira J. (Author) , Schneider, Karen (Author) , Jobst-Schwan, Tilman (Author) , Ekici, Arif B. (Author) , Uebe, Steffen (Author) , Wenzel, Andrea (Author) , Schliep, Stefan (Author) , Schürfeld, Carsten (Author) , Seitz, Randolf (Author) , Bernhardt, Wanja (Author) , Gödel, Markus (Author) , Wiesener, Antje (Author) , Popp, Bernt (Author) , Stark, Klaus J. (Author) , Gröne, Hermann-Josef (Author) , Friedrich, Björn (Author) , Weiß, Martin (Author) , Basic-Jukic, Nikolina (Author) , Schiffer, Mario (Author) , Schröppel, Bernd (Author) , Huettel, Bruno (Author) , Beck, Bodo B. (Author) , Sayer, John A. (Author) , Ziegler, Christine (Author) , Büttner-Herold, Maike (Author) , Amann, Kerstin (Author) , Heid, Iris M. (Author) , Reis, André (Author) , Pasutto, Francesca (Author) , Wiesener, Michael S. (Author) ,


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  4. 4
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    Long-term data on two sisters with C3GN due to an identical, homozygous CFH mutation and autoantibodies by Hackl, Agnes (Author) , Erger, Florian (Author) , Skerka, Christine (Author) , Wenzel, Andrea (Author) , Tschernoster, Nikoai (Author) , Ehren, Rasmus (Author) , Burgmaier, Kathrin (Author) , Riehmer, Vera (Author) , Licht, Christoph (Author) , Kirschfink, Michael (Author) , Weber, Lutz T. (Author) , Altmüller, Janine (Author) , Zipfel, Peter F. (Author) , Habbig, Sandra (Author) ,


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