Efficacy and safety of adjunctive ezogabine (retigabine) in refractory partial epilepsy von BRODIE, M. J, LERCHE, H, GIL-NAGEL, A, ELGER, C, HALL, S, SHIN, P, NOHRIA, V, MANSBACH, H

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Non-invasive in-cell determination of free cytosolic [NAD+]/[NADH] ratios using hyperpolarized glucose show large variations in metabolic phenotypes von Christensen, Caspar Elo, Karlsson, Magnus, Winther, Jakob R, Jensen, Pernille Rose, Lerche, Mathilde H

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Increase in Signal-to-Noise Ratio of >10,000 Times in Liquid-State NMR von Ardenkjær-Larsen, Jan H., Fridlund, Björn, Gram, Andreas, Hansson, Georg, Hansson, Lennart, Lerche, Mathilde H., Servin, Rolf, Thaning, Mikkel, Golman, Klaes

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Hyperpolarized NMR probes for biological assays von Meier, Sebastian, Jensen, Pernille R, Karlsson, Magnus, Lerche, Mathilde H

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Transcutaneous Vagus Nerve Stimulation (tVNS) for Treatment of Drug-Resistant Epilepsy: A Randomized, Double-Blind Clinical Trial (cMPsE02) von Bauer, S, Baier, H, Baumgartner, C, Bohlmann, K, Fauser, S, Graf, W, Hillenbrand, B, Hirsch, M, Last, C, Lerche, H, Mayer, T, Schulze-Bonhage, A, Steinhoff, B.J, Weber, Y, Hartlep, A, Rosenow, F, Hamer, H.M

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Production of hyperpolarized [1,4-¹³C₂]malate from [1,4-¹³C₂]fumarate is a marker of cell necrosis and treatment response in tumors von Gallagher, Ferdia A, Kettunen, Mikko I, Hu, De-En, Jensen, Pernille R, Zandt, René in 't, Karlsson, Magnus, Gisselsson, Anna, Nelson, Sarah K, Witney, Timothy H, Bohndiek, Sarah E, Hansson, Georg, Peitersen, Torben, Lerche, Mathilde H, Brindle, Kevin M

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Comparative analysis of brain structure, metabolism, and cognition in myotonic dystrophy 1 and 2 von WEBER, Y. G, ROEBLING, R, LEHMANN-HORN, F, MOTTAGHY, F. M, LERCHE, H, KASSUBEK, J, HOFFMANN, S, ROSENBOHM, A, WOLF, M, STEINBACH, P, JURKAT-ROTT, K, WALTER, H, RESKE, S. N

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Mutations in the sodium channel gene SCN2A cause neonatal epilepsy with late-onset episodic ataxia von Schwarz, N., Hahn, A., Bast, T., Müller, S., Löffler, H., Maljevic, S., Gaily, E., Prehl, I., Biskup, S., Joensuu, T., Lehesjoki, A.-E., Neubauer, B. A., Lerche, H., Hedrich, U. B. S.

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Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1 von Suls, Arvid, Dedeken, Peter, Goffin, Karolien, Van Esch, Hilde, Dupont, Patrick, Cassiman, David, Kempfle, Judith, Wuttke, Thomas V., Weber, Yvonne, Lerche, Holger, Afawi, Zaid, Vandenberghe, Wim, Korczyn, Amos D., Berkovic, Samuel F., Ekstein, Dana, Kivity, Sara, Ryvlin, Philippe, Claes, Lieve R. F., Deprez, Liesbet, Maljevic, Snezana, Vargas, Alberto, Van Dyck, Tine, Goossens, Dirk, Del-Favero, Jurgen, Van Laere, Koen, De Jonghe, Peter, Van Paesschen, Wim

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Understanding the climatic signal in the water stable isotope records from the NEEM shallow firn/ice cores in northwest Greenland von Steen-Larsen, H. C., Masson-Delmotte, V., Sjolte, J., Johnsen, S. J., Vinther, B. M., Bréon, F.-M., Clausen, H. B., Dahl-Jensen, D., Falourd, S., Fettweis, X., Gallée, H., Jouzel, J., Kageyama, M., Lerche, H., Minster, B., Picard, G., Punge, H. J., Risi, C., Salas, D., Schwander, J., Steffen, K., Sveinbjörnsdóttir, A. E., Svensson, A., White, J.

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Metabolic pathway visualization in living yeast by DNP-NMR von Meier, Sebastian, Karlsson, Magnus, Jensen, Pernille R, Lerche, Mathilde H, Duus, Jens Ø

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Peripheral nerve hyperexcitability due to dominant-negative KCNQ2 mutations von WUTTKE, T. V, JURKAT-ROTT, K, PAULUS, W, GARNCAREK, M, LEHMANN-HORN, F, LERCHE, H

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SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain von LIAO, Y, ANTTONEN, A.-K, LEHESJOKI, A.-E, LIUKKONEN, E, GAILY, E, MALJEVIC, S, SCHUBERT, S, BELLAN-KOCH, A, PETROU, S, AHONEN, V. E, LERCHE, H

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Hyperpolarized [1,3‐13C2]ethyl acetoacetate is a novel diagnostic metabolic marker of liver cancer von Jensen, Pernille R., Serra, Sonia Colombo, Miragoli, Luigi, Karlsson, Magnus, Cabella, Claudia, Poggi, Luisa, Venturi, Luca, Tedoldi, Fabio, Lerche, Mathilde H.

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Tissue-specific Short Chain Fatty Acid Metabolism and Slow Metabolic Recovery after Ischemia from Hyperpolarized NMR in Vivo von Jensen, Pernille R., Peitersen, Torben, Karlsson, Magnus, in 't Zandt, René, Gisselsson, Anna, Hansson, Georg, Meier, Sebastian, Lerche, Mathilde H.

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Clinical and genetic spectrum of SCN2A-associated episodic ataxia von Schwarz, N., Bast, T., Gaily, E., Golla, G., Gorman, K.M., Griffiths, L.R., Hahn, A., Hukin, J., King, M., Korff, C., Miranda, M.J., Møller, R.S., Neubauer, B., Smith, R.A., Smol, T., Striano, P., Stroud, B., Vaccarezza, M., Kluger, G., Lerche, H., Fazeli, W.

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Hyperpolarized Amino Acids for In Vivo Assays of Transaminase Activity von Jensen, Pernille R., Karlsson, Magnus, Meier, Sebastian, Duus, Jens Ø., Lerche, Mathilde H.

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P97. The pathophysiology of sudden unexpected death in epilepsy (SUDEP) von Lauxmann, S, Weber, Y, Lerche, H, Koch, H

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Development of Dissolution DNP-MR Substrates for Metabolic Research von Karlsson, Magnus, Jensen, Pernille R., Duus, Jens Ø., Meier, Sebastian, Lerche, Mathilde H.

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Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect von WEBER, Y. G, KAMM, C, LUDOLPH, A. C, VAN PAESSCHEN, W, SCHÖLS, L, DE JONGHE, P, AUBURGER, G, LERCHE, H, SULS, A, KEMPFLE, J, KOTSCHET, K, SCHÜLE, R, WUTTKE, T. V, MALJEVIC, S, LIEBRICH, J, GASSER, T

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