Search Results - Nürnberg, Gudrun

Novel findings in patients with primary hyperoxaluria type III and implications for advanced molecular testing strategies by Beck, Bodo Bernhard (Author) , Baasner, Anne (Author) , Buescher, Anja (Author) , Habbig, Sandra (Author) , Reintjes, Nadine (Author) , Kemper, Markus J. (Author) , Sikora, Przemyslaw (Author) , Mache, Christoph (Author) , Pohl, Martin (Author) , Stahl, Mirjam (Author) , Tönshoff, Burkhard (Author) , Pape, Lars (Author) , Fehrenbach, Henry (Author) , Jacob, Dorrit E. (Author) , Grohe, Bernd (Author) , Wolf, Matthias T. (Author) , Nürnberg, Gudrun (Author) , Yigit, Gökhan (Author) , Salido, Eduardo C. (Author) , Hoppe, Bernd (Author) ,

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Impaired epidermal ceramide synthesis causes autosomal recessive congenital ichthyosis and reveals the importance of ceramide acyl chain length by Eckl, Katja Martina (Author) , Tidhar, Rotem (Author) , Thiele, Holger (Author) , Oji, Vinzenz (Author) , Haußer-Siller, Ingrid (Author) , Brodesser, Susanne (Author) , Preil, Marie-Luise (Author) , Önal-Akan, Aysel (Author) , Stock, Friedrich (Author) , Müller, Dietmar (Author) , Becker, Kerstin (Author) , Casper, Ramona (Author) , Nürnberg, Gudrun (Author) , Altmüller, Janine (Author) , Nürnberg, Peter (Author) , Traupe, Heiko (Author) , Futerman, Anthony H. (Author) , Hennies, Hans C. (Author) ,

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Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome by Lemaire, Mathieu (Author) , Frémeaux-Bacchi, Véronique (Author) , Schaefer, Franz (Author) , Choi, Murim (Author) , Tang, Wai Ho (Author) , Le Quintrec, Moglie (Author) , Fakhouri, Fadi (Author) , Taque, Sophie (Author) , Nobili, François (Author) , Martinez, Frank (Author) , Ji, Weizhen (Author) , Overton, John D. (Author) , Mane, Shrikant M. (Author) , Nürnberg, Gudrun (Author) , Altmüller, Janine (Author) , Thiele, Holger (Author) , Morin, Denis (Author) , Deschenes, Georges (Author) , Baudouin, Véronique (Author) , Llanas, Brigitte (Author) , Collard, Laure (Author) , Majid, Mohammed A. (Author) , Simkova, Eva (Author) , Nürnberg, Peter (Author) , Rioux-Leclerc, Nathalie (Author) , Moeckel, Gilbert W. (Author) , Gubler, Marie Claire (Author) , Hwa, John (Author) , Loirat, Chantal (Author) , Lifton, Richard P. (Author) ,

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Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease by Oji, Vinzenz (Author) , Eckl, Katja-Martina (Author) , Aufenvenne, Karin (Author) , Nätebus, Marc (Author) , Tarinski, Tatjana (Author) , Ackermann, Katharina (Author) , Seller, Natalia (Author) , Metze, Dieter (Author) , Nürnberg, Gudrun (Author) , Fölster-Holst, Regina (Author) , Schäfer-Korting, Monika (Author) , Haußer-Siller, Ingrid (Author) , Traupe, Heiko (Author) , Hennies, Hans Christian (Author) ,

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