Engineered coumarin accumulation reduces mycotoxin‐induced oxidative stress and disease susceptibility by Beesley, Alexander, Beyer, Sebastian F., Wanders, Verena, Levecque, Sophie, Bredenbruch, Sandra, Habash, Samer S., Schleker, A. Sylvia S., Gätgens, Jochem, Oldiges, Marco, Schultheiss, Holger, Conrath, Uwe, Langenbach, Caspar J. G.

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Methylene Blue Treatment of Grafts During Cold Ischemia Time Reduces the Risk of Hepatitis C Virus Transmission by Helfritz, Fabian A, Bojkova, Denisa, Wanders, Verena, Kuklinski, Nina, Westhaus, Sandra, von Horn, Charlotte, Rauen, Ursula, Gallinat, Anja, Baba, Hideo A, Skyschally, Andreas, Swoboda, Sandra, Kinast, Volker, Steinmann, Eike, Heusch, Gerd, Minor, Thomas, Meuleman, Philip, Paul, Andreas, Ciesek, Sandra

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Infectivity and stability of hepatitis C virus in different perfusion solutions by Helfritz, Fabian A., Wanders, Verena, Bojkova, Denisa, Kuklinski, Nina, Westhaus, Sandra, Swoboda, Sandra, Minor, Thomas, Meuleman, Philip, Paul, Andreas, Steinmann, Eike, Ciesek, Sandra

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An international classification of inherited metabolic disorders (ICIMD) by Ferreira, Carlos R., Rahman, Shamima, Keller, Markus, Zschocke, Johannes, Abdenur, Jose, Ali, Houda, Artuch, Rafael, Ballabio, Andrea, Barshop, Bruce, Baumgartner, Matthias, Bertini, Enrico Silvio, Blau, Nenad, Carelli, Valerio, Carroll, Christopher, Chinnery, Patrick F., Christodoulou, John, Cornejo, Veronica, Darin, Niklas, Derks, Terry, Diodato, Daria, Dionisi‐Vici, Carlo, Duley, John A., Fukao, † Toshi, García‐Cazorla, Ángeles, Giugliani, Roberto, Goldstein, Amy, Hoffmann, Georg, Horvath, Rita, Ibarra, Isabel, Inwood, Anita, Jaeken, Jaak, Jimenez‐Mallebrera, Cecilia, Karaa, Amel, Klopstock, Thomas, Kölker, Stefan, Kornblum, Cornelia, Kožich, Viktor, Lamperti, Costanza, Larsson, Nils‐Göran, Lemes, Aida, Lewis, Barry, Mancuso, Michelangelo, McFarland, Robert, Mochel, Fanny, Montoya, Julio, Morava, Eva, Naess, Karin, Okuyama, Torayuki, Olry, Annie, Paquis‐Flucklinger, Veronique, Parikh, Sumit, Patterson, Marc, Pérez de Ferrán, Ceila, Peters, Verena, Prokisch, Holger, Saada, Ann, Salomons, Gajja S., Saudubray, Jean‐Marie, Scarpa, Maurizio, Schara‐Schmidt, Ulrike, Schiff, Manuel, Servidei, Serenella, Smeitink, Jan, Suomalainen, Anu, Tangeraas, Trine, Taylor, Robert W., Thiele, Ines, Thorburn, David, Hove, Johan, der Ploeg, Ans T., Karnebeek, Clara, Visser, Gepke, Vockley, Jerry, Wanders, Ronald, Webster, Dianne, Wedell, Anna, Wiley, Veronica, Wredenberg, Anna, Zeviani, Massimo

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Stability of the ABCD1 Protein with a Missense Mutation: A Novel Approach to Finding Therapeutic Compounds for X-Linked Adrenoleukodystrophy by Morita, Masashi, Matsumoto, Shun, Sato, Airi, Inoue, Kengo, Kostsin, Dzmitry G., Yamazaki, Kozue, Kawaguchi, Kosuke, Shimozawa, Nobuyuki, Kemp, Stephan, Wanders, Ronald J., Kojima, Hirotatsu, Okabe, Takayoshi, Imanaka, Tsuneo

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Necrotizing Enterocolitis and Respiratory Distress Syndrome as First Clinical Presentation of Mitochondrial Trifunctional Protein Deficiency by Diekman, Eugène F., Boelen, Carolien C. A., Prinsen, Berthil H. C. M. T., IJlst, Lodewijk, Duran, Marinus, de Koning, Tom J., Waterham, Hans R., Wanders, Ronald J. A., Wijburg, Frits A., Visser, Gepke

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Novel PEX3 Gene Mutations Resulting in a Moderate Zellweger Spectrum Disorder by Maxit, C., Denzler, I., Marchione, D., Agosta, G., Koster, J., Wanders, R. J. A., Ferdinandusse, S., Waterham, H. R.

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Two Novel Mutations in the SLC25A4 Gene in a Patient with Mitochondrial Myopathy by Körver-Keularts, I. M. L. W., de Visser, M., Bakker, H. D., Wanders, R. J. A., Vansenne, F., Scholte, H. R., Dorland, L., Nicolaes, G. A. F., Spaapen, L. M. J., Smeets, H. J. M., Hendrickx, A. T. M., van den Bosch, B. J. C.

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