Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study von Mothes-Luksch, N, Jordakieva, G, Hinterhölzl, L, Jensen, A N, Hallmann, P K, Kundi, M, Jensen-Jarolim, E

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O.24 Loss of function of MGME1, a novel player in mitochondrial DNA replication, causes a distinct autosomal recessive mitochondrial disorder von Kornblum, C, Nicholls, T, Haack, T.B, Schoeler, S, Peeva, V, Danhauser, K, Hallmann, K, Zsurka, G, Rorbach, J, Iuso, A, Wieland, T, Sciacco, M, Ronchi, D, Comi, G.P, Moggio, M, Quinzii, C.M, DiMauro, S, Calvo, S.E, Mootha, V.K, Klopstock, T, Strom, T.M, Meitinger, T, Minczuk, M, Kunz, W.S, Prokisch, H

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Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies von de Kovel, Carolien G. F., Trucks, Holger, Helbig, Ingo, Mefford, Heather C., Baker, Carl, Leu, Costin, Kluck, Christian, Muhle, Hiltrud, von Spiczak, Sarah, Ostertag, Philipp, Obermeier, Tanja, Kleefuß-Lie, Ailing A., Hallmann, Kerstin, Steffens, Michael, Gaus, Verena, Klein, Karl M., Hamer, Hajo M., Rosenow, Felix, Brilstra, Eva H., Kasteleijn-Nolst Trenité, Dorothée, Swinkels, Marielle E. M., Weber, Yvonne G., Unterberger, Iris, Zimprich, Fritz, Urak, Lydia, Feucht, Martha, Fuchs, Karoline, Møller, Rikke S., Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Rückert, Ina-Maria, Wichmann, Heinz-Erich, Franke, Andre, Schreiber, Stefan, Nürnberg, Peter, Elger, Christian E., Lerche, Holger, Stephani, Ulrich, Koeleman, Bobby P. C., Lindhout, Dick, Eichler, Evan E., Sander, Thomas

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Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance von Dibbens, Leanne M., Mullen, Saul, Helbig, Ingo, Mefford, Heather C., Bayly, Marta A., Bellows, Susannah, Leu, Costin, Trucks, Holger, Obermeier, Tanja, Wittig, Michael, Franke, Andre, Caglayan, Hande, Yapici, Zuhal, Sander, Thomas, Eichler, Evan E., Scheffer, Ingrid E., Mulley, John C., Berkovic, Samuel F.

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A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family von LEE, W. L, BIERVERT, C, HALLMANN, K, TAY, A, DEAN, J. C. S, STEINLEIN, O. K

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Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies von Alekov, Alexi K, Rau, Birgit, Hebeisen, Simon, Propping, Peter, Haverkamp, Fritz, Janz, Dieter, Fahlke, Christoph, Maljevic, Snezana, Beyenburg, Stefan, Haug, Karsten, Dullinger, Joern S, Kubisch, Christian, Lerche, Holger, Elger, Christian E, Ramírez, Alfredo, Horvath, Steve, Müller-Newen, Gerhard, Rebstock, Johannes, Heils, Armin, Warnstedt, Maike, Hallmann, Kerstin, Poser, Barbara, Giese, Bernd, Sander, Thomas, Schulz, Herbert

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The voltage-gated sodium channel β2-subunit gene and idiopathic generalized epilepsy von Haug, Karsten, Sander, Thomas, Hallmann, Kerstin, Rau, Birgit, Dullinger, Joern S, Elger, Christian E, Propping, Peter, Heils, Armin

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Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy von Haug, K, Kremerskothen, J, Hallmann, K, Sander, T, Dullinger, J, Rau, B, Beyenburg, S, Lentze, M.J, Barnekow, A, Elger, C.E, Propping, P, Heils, A

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The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy von Haug, Karsten, Hallmann, Kerstin, Rebstock, Johannes, Dullinger, Joern, Muth, Sabine, Haverkamp, Fritz, Pfeiffer, Heike, Rau, Birgit, Elger, Christian Erich, Propping, Peter, Heils, Armin

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Mutation analysis of the inwardly rectifying K+ channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy von Hallmann, Kerstin, Durner, Martina, Sander, Thomas, Steinlein, Ortrud K.

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The voltage-gated sodium channel beta 2-subunit gene and idiopathic generalized epilepsy von Haug, K, Sander, T, Hallmann, K, Rau, B, Dullinger, J S, Elger, CE, Propping, P, Heils, A

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The voltage-gated sodium channel beta2-subunit gene and idiopathic generalized epilepsy von Haug, K, Sander, T, Hallmann, K, Rau, B, Dullinger, J S, Elger, C E, Propping, P, Heils, A

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No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy von Haug, Karsten, Hallmann, Kerstin, Horvath, Steve, Sander, Thomas, Kubisch, Christian, Rau, Birgit, Dullinger, Joern, Beyenburg, Stefan, Elger, Christian Erich, Propping, Peter, Heils, Armin

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Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy von Haug, Karsten, Sander, Thomas, Hallmann, Kerstin, Lentze, Michael J., Propping, Peter, Elger, Christian Erich, Heils, Armin

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A KCNQ2 Splice Site Mutation Causing Benign Neonatal Convulsions in a Scottish Family von Lee, W. L., Biervert, C., Hallmann, K., Tay, A., Dean, J. C.S., Steinlein, O. K.

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Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A von Kasperaviciute, D, Catarino, CB, Matarin, M, Leu, C, Novy, J, Tostevin, A, Leal, B, Hessel, EV, Hallmann, K, Hildebrand, MS, Dahl, HH, Ryten, M, Trabzuni, D, Ramasamy, A, Alhusaini, S, Doherty, CP, Dorn, T, Hansen, J, Krämer, G, Steinhoff, BJ, Zumsteg, D, Duncan, S, Kälviäinen, RK, Eriksson, KJ, Kantanen, AM, Pandolfo, M, Gruber-Sedlmayr, U, Schlachter, K, Reinthaler, EM, Stogmann, E, Zimprich, F, Théâtre, E, Smith, C, O'Brien, TJ, Meng Tan, K, Petrovski, S, Robbiano, A, Paravidino, R, Zara, F, Striano, P, Sperling, MR, Buono, RJ, Hakonarson, H, Chaves, J, Costa, PP, Silva, BM, da Silva, AM, de Graan, PN, Koeleman, BP, Becker, A, Schoch, S, von Lehe, M, Reif, PS, Rosenow, F, Becker, F, Weber, Y, Lerche, H, Rössler, K, Buchfelder, M, Hamer, HM, Kobow, K, Coras, R, Blumcke, I, Scheffer, IE, Berkovic, SF, Weale, ME, UK Brain Expression Consortium, The, Delanty, N, Depondt, C, Cavalleri, GL, Kunz, WS, Sisodiya, SM

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Development of a hard X-ray split-and-delay line and performance simulations for two-color pump-probe experiments at the European XFEL von Lu, W., Friedrich, B., Noll, T., Zhou, K., Hallmann, J., Ansaldi, G., Roth, T., Serkez, S., Geloni, G., Madsen, A., Eisebitt, S.

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Silver and palladium help unveil the nature of a second r-process von Hansen, C. J., Primas, F., Hartman, H., Kratz, K.-L., Wanajo, S., Leibundgut, B., Farouqi, K., Hallmann, O., Christlieb, N., Nilsson, H.

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Materials Imaging and Dynamics (MID) instrument at the European X‐ray Free‐Electron Laser Facility von Madsen, A., Hallmann, J., Ansaldi, G., Roth, T., Lu, W., Kim, C., Boesenberg, U., Zozulya, A., Möller, J., Shayduk, R., Scholz, M., Bartmann, A., Schmidt, A., Lobato, I., Sukharnikov, K., Reiser, M., Kazarian, K., Petrov, I.

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Limits on dark matter annihilation in the sun using the ANTARES neutrino telescope von Adrián-Martínez, S., Albert, A., André, M., Ardid, M., Aubert, J.-J., Avgitas, T., Baret, B., Barrios-Martí, J., Basa, S., Bertin, V., Biagi, S., Bormuth, R., Bouwhuis, M.C., Bruijn, R., Brunner, J., Busto, J., Caramete, L., Carr, J., Celli, S., Circella, M., Coleiro, A., Coniglione, R., Costantini, H., Coyle, P., Creusot, A., Deschamps, A., De Bonis, G., Distefano, C., Donzaud, C., Dornic, D., Drouhin, D., El Bojaddaini, I., Enzenhöfer, A., Fehn, K., Felis, I., Galatà, S., Gay, P., Geißelsöder, S., Geyer, K., Giordano, V., Gleixner, A., Glotin, H., Gracia-Ruiz, R., Graf, K., Hallmann, S., van Haren, H., Heijboer, A.J., Hello, Y., Hernández-Rey, J.J., Hößl, J., Hofestädt, J., Hugon, C., Illuminati, G., James, C.W., de Jong, M., Jongen, M., Kadler, M., Kalekin, O., Katz, U., Kießling, D., Kreter, M., Kreykenbohm, I., Lachaud, C., Lahmann, R., Lefèvre, D., Marcelin, M., Margiotta, A., Martínez-Mora, J.A., Mathieu, A., Michael, T., Migliozzi, P., Moussa, A., Mueller, C., Nezri, E., Pellegrino, C., Perrina, C., Popa, V., Pradier, T., Racca, C., Riccobene, G., Sánchez-Losa, A., Sapienza, P., Schnabel, J., Schüssler, F., Seitz, T., Sieger, C., Spurio, M., Stolarczyk, Th, Taiuti, M., Tönnis, C., Trovato, A., Tselengidou, M., Turpin, D., Vallée, C., Van Elewyck, V., Vivolo, D., Wagner, S., Wilms, J., Zornoza, J.D., Zúñiga, J.

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