A randomized controlled trial of the effect of spironolactone on left ventricular mass in hemodialysis patients by Hammer, Fabian, Malzahn, Uwe, Donhauser, Julian, Betz, Christoph, Schneider, Markus P., Grupp, Clemens, Pollak, Nils, Störk, Stefan, Wanner, Christoph, Krane, Vera, Berweck, Susanne, Biggar, Patrick, Blaser, Christoph, Bochannek, Thomas, Breunig, Frank, Brunner, Michael, Büschges-Seraphin, Beatrix, Büttner, Stefan, Cakmak, Ahmet, Döltz, Thomas, Dörken, Mara, Eckardt, Kai-Uwe, Fink, Heribert, Fischer, Stefan, Freisinger, Wolfgang, Freiwald, Tilo, Gebhardt, Julian, Geiger, Helmut, Götz, Rüdiger, Goßmann, Jan, Hammerstingl, Renate, Harazny, Joanna, Heckel, Michael, Heyd-Schramm, Andrea, Hoyer, Joachim, Janka, Rolf, Jung, Oliver, Ketteler, Markus, Klaeffling, Christina, Kleinert, Claudius, Kleinert, Marianne, Klingbeil, Arnfried, Klink, Thorsten, Koch, Benjamin-Florian, Kosowski, Judith, Leidig, Michael, Lutz, Jens, Marwan, Mohamed, Moritz, Maria, Moye, Brigitte, Naujoks, Holger, Netzer, Kai-Olaf, Raff, Ulrike, Reichert, Clemens, Reimer, Imke, Ribel, Jurij, Richter, Sophie, Ritter, Christian, Rudolf, Sarah, Schamberger, Beate, Schmid, Michael, Schmiedeke, Thomas, Schmitt, Andreas, Schneider, Heike, Schneider, Reinhard, Schneuzer, Cord, Schöffauer, Markus, Schramm, Lothar, Schütterle, Sabine, Schwedler, Susanne, Sobkowiak, Ewelina, Sollinger, Daniel, Strutz, Frank, Toncar, Sebastian, Vasiljuk, Vladimir, Vogl, Thomas, Walther, Thorsten, Weinmann-Menke, Julia, Wirth, Bettina, Witsch, Hendrick, Würmell, Paul, Zeltner, Raoul, Zimmermann, Josef

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The effect of spironolactone on diastolic function in haemodialysis patients by Hauser, T., Dornberger, V., Malzahn, U., Grebe, S. J., Liu, D., Störk, S., Nauck, M., Friedrich, N., Dörr, M., Wanner, C., Krane, V., Hammer, F.

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Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings by Haack, Tobias B., Rolinski, Boris, Haberberger, Birgit, Zimmermann, Franz, Schum, Jessica, Strecker, Valentina, Graf, Elisabeth, Athing, Uwe, Hoppen, Thomas, Wittig, Ilka, Sperl, Wolfgang, Freisinger, Peter, Mayr, Johannes A., Strom, Tim M., Meitinger, Thomas, Prokisch, Holger

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The spectrum of pyruvate oxidation defects in the diagnosis of mitochondrial disorders by Sperl, Wolfgang, Fleuren, Leanne, Freisinger, Peter, Haack, Tobias B., Ribes, Antonia, Feichtinger, René G., Rodenburg, Richard J., Zimmermann, Franz A., Koch, Johannes, Rivera, Isabel, Prokisch, Holger, Smeitink, Jan A., Mayr, Johannes A.

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Mitochondrial Phosphate–Carrier Deficiency: A Novel Disorder of Oxidative Phosphorylation by Mayr, Johannes A., Merkel, Olaf, Kohlwein, Sepp D., Gebhardt, Boris R., Böhles, Hansjosef, Fötschl, Ulrike, Koch, Johannes, Jaksch, Michaela, Lochmüller, Hanns, Horváth, Rita, Freisinger, Peter, Sperl, Wolfgang

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Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy by Gai, Xiaowu, Ghezzi, Daniele, Johnson, Mark A., Biagosch, Caroline A., Shamseldin, Hanan E., Haack, Tobias B., Reyes, Aurelio, Tsukikawa, Mai, Sheldon, Claire A., Srinivasan, Satish, Gorza, Matteo, Kremer, Laura S., Wieland, Thomas, Strom, Tim M., Polyak, Erzsebet, Place, Emily, Consugar, Mark, Ostrovsky, Julian, Vidoni, Sara, Robinson, Alan J., Wong, Lee-Jun, Sondheimer, Neal, Salih, Mustafa A., Al-Jishi, Emtethal, Raab, Christopher P., Bean, Charles, Furlan, Francesca, Parini, Rossella, Lamperti, Costanza, Mayr, Johannes A., Konstantopoulou, Vassiliki, Huemer, Martina, Pierce, Eric A., Meitinger, Thomas, Freisinger, Peter, Sperl, Wolfgang, Prokisch, Holger, Alkuraya, Fowzan S., Falk, Marni J., Zeviani, Massimo

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Thiamine Pyrophosphokinase Deficiency in Encephalopathic Children with Defects in the Pyruvate Oxidation Pathway by Mayr, Johannes A., Freisinger, Peter, Schlachter, Kurt, Rolinski, Boris, Zimmermann, Franz A., Scheffner, Thomas, Haack, Tobias B., Koch, Johannes, Ahting, Uwe, Prokisch, Holger, Sperl, Wolfgang

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Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation by Honzík, Tomáš, Tesařová, Markéta, Mayr, Johannes A, Hansíková, Hana, Ješina, Pavel, Bodamer, Olaf, Koch, Johannes, Magner, Martin, Freisinger, Peter, Huemer, Martina, Kostková, Olga, van Coster, Rudy, Kmoch, Stanislav, Houštêk, Josef, Sperl, Wolfgang, Zeman, Jiří

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Biallelic variants in WARS2 encoding mitochondrial tryptophanyl‐tRNA synthase in six individuals with mitochondrial encephalopathy by Wortmann, Saskia B., Timal, Sharita, Venselaar, Hanka, Wintjes, Liesbeth T., Kopajtich, Robert, Feichtinger, René G., Onnekink, Carla, Mühlmeister, Mareike, Brandt, Ulrich, Smeitink, Jan A., Veltman, Joris A., Sperl, Wolfgang, Lefeber, Dirk, Pruijn, Ger, Stojanovic, Vesna, Freisinger, Peter, v Spronsen, Francjan, Derks, Terry GJ, Veenstra‐Knol, Hermine E., Mayr, Johannes A, Rötig, Agnes, Tarnopolsky, Mark, Prokisch, Holger, Rodenburg, Richard J.

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Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening by Haack, Tobias B., Gorza, Matteo, Danhauser, Katharina, Mayr, Johannes A., Haberberger, Birgit, Wieland, Thomas, Kremer, Laura, Strecker, Valentina, Graf, Elisabeth, Memari, Yasin, Ahting, Uwe, Kopajtich, Robert, Wortmann, Saskia B., Rodenburg, Richard J., Kotzaeridou, Urania, Hoffmann, Georg F., Sperl, Wolfgang, Wittig, Ilka, Wilichowski, Ekkehard, Schottmann, Gudrun, Schuelke, Markus, Plecko, Barbara, Stephani, Ulrich, Strom, Tim M., Meitinger, Thomas, Prokisch, Holger, Freisinger, Peter

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Clinical, morphological, biochemical, imaging and outcome parameters in 21 individuals with mitochondrial maintenance defect related to FBXL4 mutations by Huemer, Martina, Karall, Daniela, Schossig, Anna, Abdenur, Jose E., Al Jasmi, Fatma, Biagosch, Caroline, Distelmaier, Felix, Freisinger, Peter, Graham, Brett H., Haack, Tobias B., Hauser, Natalie, Hertecant, Jozef, Ebrahimi-Fakhari, Darius, Konstantopoulou, Vassiliki, Leydiker, Karen, Lourenco, Charles M., Scholl-Bürgi, Sabine, Wilichowski, Ekkehard, Wolf, Nicole I., Wortmann, Saskia B., Taylor, Robert W., Mayr, Johannes A., Bonnen, Penelope E., Sperl, Wolfgang, Prokisch, Holger, McFarland, Robert

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Deficiency of the mitochondrial phosphate carrier presenting as myopathy and cardiomyopathy in a family with three affected children by Mayr, Johannes A, Zimmermann, Franz A, Horváth, Rita, Schneider, Hans-Christian, Schoser, Benedikt, Holinski-Feder, Elke, Czermin, Birgit, Freisinger, Peter, Sperl, Wolfgang

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Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype by Koch, Johannes, Freisinger, Peter, Feichtinger, René G, Zimmermann, Franz A, Rauscher, Christian, Wagentristl, Hans P, Konstantopoulou, Vassiliki, Seidl, Rainer, Haack, Tobias B, Prokisch, Holger, Ahting, Uwe, Sperl, Wolfgang, Mayr, Johannes A, Maier, Esther M

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