A novel mutation causing DEND syndrome : A treatable channelopathy of pancreas and brain von SHIMOMURA, K, HORSTER, F, DE WET, H, FLANAGAN, S. E, ELLARD, S, HATTERSLEY, A. T, WOLF, N. I, ASHCROFT, F, EBINGER, F

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Aromatic l-amino acid decarboxylase deficiency: clinical features, drug therapy and follow-up von Manegold, C, Hoffmann, G. F, Degen, I, Ikonomidou, H, Knust, A, Laaß, M. W, Pritsch, M, Wilichowski, E, Hörster, F

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Neurodegeneration and chronic renal failure in methylmalonic aciduria—A pathophysiological approach von Morath, M. A., Okun, J. G., Müller, I. B., Sauer, S. W., Hörster, F., Hoffmann, G. F., Kölker, S.

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Genotypic and phenotypic spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency von Goetz, M., Schröter, J., Dattner, T., Brennenstuhl, H., Lenz, D., Opladen, T., Hörster, F., Okun, J.G., Hoffmann, G.F., Kölker, S., Staufner, C.

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Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters von Hörster, F, Garbade, S. F, Zwickler, T, Aydin, H. I, Bodamer, O. A, Burlina, A. B, Das, A. M, De Klerk, J. B. C, Dionisi-Vici, C, Geb, S, Gökcay, G, Guffon, N, Maier, E. M, Morava, E, Walter, J. H, Schwahn, B, Wijburg, F. A, Lindner, M, Grünewald, S, Baumgartner, M. R, Kölker, S

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Ethanol-Induced Apoptotic Neurodegeneration and Fetal Alcohol Syndrome von Ikonomidou, Chrysanthy, Bittigau, Petra, Ishimaru, Masahiko J., Wozniak, David F., Koch, Christian, Genz, Kerstin, Price, Madelon T., Stefovska, Vanya, Hörster, Friederike, Tenkova, Tanya, Dikranian, Krikor, Olney, John W.

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Moderate Weight Reduction in an Outpatient Obesity Intervention Program Significantly Reduces Insulin Resistance and Risk Factors for Cardiovascular Disease in Severely Obese Adole... von Grulich-Henn, J, Lichtenstein, S, Hörster, F, Hoffmann, G F, Nawroth, P P, Hamann, A

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Looking beyond the basal ganglia: The spectrum of MRI changes in methylmalonic acidaemia von Harting, I., Seitz, A., Geb, S., Zwickler, T., Porto, L., Lindner, M., Kölker, S., Hörster, F.

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Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centres von Zwickler, T., Lindner, M., Aydin, H. I., Baumgartner, M. R., Bodamer, O. A., Burlina, A. B., Das, A. M., deKlerk, J. B. C., Gökcay, G., Grünewald, S., Guffon, N., Maier, E. M., Morava, E., Geb, S., Schwahn, B., Walter, J. H., Wendel, U., Wijburg, F. A., Müller, E., Kölker, S., Hörster, F.

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Coenzyme Q₁₀ is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria von Haas, D, Niklowitz, P, Hörster, F, Baumgartner, E. R, Prasad, C, Rodenburg, R. J, Hoffmann, G. F, Menke, T, Okun, J. G

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Disorders of intermediary metabolism: Toxic leukoencephalopathies von Hörster, F., Surtees, R., Hoffmann, G. F.

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Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea‐cycle disorders: On the basis of information from a European multicenter registry von Molema, Femke, Gleich, Florian, Burgard, Peter, Ploeg, Ans T., Summar, Marshall L., Chapman, Kimberly A., Barić, Ivo, Lund, Allan M., Kölker, Stefan, Williams, Monique, Hörster, F., Jelsig, A.M., Lonlay, P., Wijburg, F.A., Bosch, A., Freisinger, P., Posset, R., Augoustides‐Savvopoulou, P., Avram, P., Deleanu, C., Baumgartner, M.R., Häberle, J., Blasco‐Alonso, J., Burlina, A.B., Rubert, L., Cazorla, A. Garcia, Saladelafont, E. Cortes i, Dionisi‐Vici, C., Martinelli, D., Dobbelaere, D., Mention, K., Grünewald, S., Chakrapani, A., Hwu, Wuh‐Liang, Chien, Yin‐Hsiu, Lee, Ni‐Chung, Karall, D., Scholl‐Bürgi, S., Lachmann, R., De Laet, C., Matsumoto, S., Meirleir, L., Mühlhausen, C., Schiff, M., Peña‐Quintana, L., Djordjevic, M., Sarajlija, A., Sykut‐Cegielska, J., Wisniewska, A., Leao‐Teles, E., Alves, S., Vara, R., Vives‐Pinera, I., Ortega, D.G., Morris, A., Zeman, J., Honzik, T., Chabrol, B., Arnaudo, F., Cano, A., Thompson, N., Eyskens, F., Lindner, M., Lüsebrink, N., Jalan, A., Sokal, E., Legros, V., Nassogne, M.C.

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Erratum to: Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters von Hörster, F., Garbade, S. F., Zwickler, T., Aydin, H. I., Bodamer, O. A., Burlina, A. B., Das, A. M., De Klerk, J. B. C., Dionisi-Vici, C., Geb, S., Gökcay, G., Guffon, N., Maier, E. M., Morava, E., Walter, J. H., Schwahn, B., Wijburg, F. A., Lindner, M., Grünewald, S., Baumgartner, M. R., Kölker, S.

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Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth re... von Molema, Femke, Gleich, Florian, Burgard, Peter, van der Ploeg, Ans T., Summar, Marshall L., Chapman, Kimberly A., Lund, Allan M., Rizopoulos, Dimitris, Kölker, Stefan, Williams, Monique, Hörster, F., Jelsig, A.M., de Lonlay, P., Wijburg, F.A., Bosch, A., Freisinger, P., Posset, R., Augoustides-Savvopoulou, P., Avram, P., Deleanu, C., Baumgartner, M.R., Häberle, J., Blasco-Alonso, J., Burlina, A.B., Rubert, L., Cazorla, A. Garcia, Saladelafont, E. Cortes I., Dionisi-Vici, C., Martinelli, D., Dobbelaere, D., Mention, K., Grünewald, S., Chakrapani, A., Hwu, Wuh-Liang, Chien, Yin-Hsiu, Lee, Ni-Chung, Karall, D., Scholl-Bürgi, S., De Laet, C., Matsumoto, S., de Meirleir, L., Schiff, M., Peña-Quintana, L., Djordjevic, M., Sarajlija, A., Sykut-Cegielska, J., Wisniewska, A., Leao-Teles, E., Alves, S., Vara, R., Vives-Pinera, I., Gil-Ortega, D., Morris, A., Zeman, J., Honzik, T., Chabrol, B., Arnaudo, F., Cano, A., Thompson, N., Eyskens, F., Lindner, M., Lüsebrink, N., Jalan, A., Sokal, E., Legros, V., Nassogne, M.C., Barić, I.

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Embryonic Renal Epithelia: Induction, Nephrogenesis, and Cell Differentiation von Horster, Michael F, Braun, Gerald S, Huber, Stephan M

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Excitotoxicity and bioenergetics in glutaryl‐CoA dehydrogenase deficiency von KÖlker, S., Koeller, D. M., Sauer, S., HÖrster, F., Schwab, M. A., Hoffmann, G. F., Ullrich, K., Okun, J. G.

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Coenzyme Q(10) is decreased in fibroblasts of patients with methylmalonic aciduria but not in mevalonic aciduria von Haas, D, Niklowitz, P, Hörster, F, Baumgartner, E R, Prasad, C, Rodenburg, R J, Hoffmann, G F, Menke, T, Okun, J G

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Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood-brain barrier constitute a biochemical risk factor for neurodegenerati... von Sauer, Sven W, Okun, Jürgen G, Fricker, Gert, Mahringer, Anne, Müller, Ines, Crnic, Linda R, Mühlhausen, Chris, Hoffmann, Georg F, Hörster, Friederike, Goodman, Stephen I, Harding, Cary O, Koeller, David M, Kölker, Stefan

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3-Ureidopropionate contributes to the neuropathology of 3-ureidopropionase deficiency and severe propionic aciduria: A hypothesis von Kölker, Stefan, Okun, Jürgen G., Hörster, Friederike, Assmann, Birgit, Ahlemeyer, Barbara, Kohlmüller, Dirk, Exner-Camps, Sonja, Mayatepek, Ertan, Krieglstein, Josef, Hoffmann, Georg F.

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Looking beyond the basal ganglia : The spectrum of MRI changes in methylmalonic acidaemia : MMA von HARTING, I, SEITZ, A, GEB, S, ZWICKLER, T, PORTO, L, LINDNER, M, KÖLKER, S, HÖRSTER, F

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