Nitrobenzene degradation in Fenton-like systems using Cu(II) as catalyst. Comparison between Cu(II)- and Fe(III)-based systems von Nichela, Daniela A., Berkovic, Andrea M., Costante, Mariana R., Juliarena, María P., García Einschlag, Fernando S.

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Combining multivariate curve resolution and lumped kinetic modelling for the analysis of lignin degradation by copper-catalyzed Fenton-like systems von Berkovic, Andrea M, Costante, Mariana R, Garca Einschlag, Fernando S

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Evaluation of the Hg2+ binding potential of fulvic acids from fluorescence excitation—emission matrices von Berkovic, Andrea M., García Einschlag, Fernando S., Gonzalez, Mónica C., Pis Diez, Reinaldo, Mártire, Daniel O.

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Photoinduced reduction of divalent mercury by quinones in the presence of formic acid under anaerobic conditions von Berkovic, Andrea M., Bertolotti, Sonia G., Villata, Laura S., Gonzalez, Mónica C., Pis Diez, Reinaldo, Mártire, Daniel O.

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Reduction of Mercury(II) by the Carbon Dioxide Radical Anion: A Theoretical and Experimental Investigation von Berkovic, Andrea M, Gonzalez, Mónica C, Russo, Nino, del Carmen Michelini, María, Diez, Reinaldo Pis, Mártire, Daniel O

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One-electron oxidation of antioxidants: A kinetic-thermodynamic correlation von Villata, Laura S., Berkovic, Andrea M., Gonzalez, Mónica C., Mártire, Daniel O.

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Assessment of nitrogen dioxide concentrations and main sources in a medium-sized city in Latin America using geographic information systems von Berkovic, Andrea M., Stadler, Carla, Fusé, Victoria S., Picone, Natasha, Ibarlucía, Daniela, Juliarena, Maria P.

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Evaluation of the Hg2+ binding potential of fulvic acids from fluorescence excitation-emission matricesElectronic supplementary information (ESI) available. See DOI: 10.1039/c2pp25... von Berkovic, Andrea M, García Einschlag, Fernando S, Gonzalez, Mónica C, Pis Diez, Reinaldo, Mártire, Daniel O

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PROCEDIMIENTO PARA EL TRATAMIENTO DE UN MEDIO ACUOSO CONTAMINADO CON METALES von MARTIRE, DANIEL O, GONZALEZ, MONICA C, BERKOVIC, ANDREA M, PIS DIEZ, REINALDO

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Hypothalamic Hamartomas: Evolving Understanding and Management von Cohen, Nathan T., Cross, J. Helen, Arzimanoglou, Alexis, Berkovic, Samuel F., Kerrigan, John F., Miller, Ilene Penn, Webster, Erica, Soeby, Lisa, Cukiert, Arthur, Hesdorffer, Dale K., Kroner, Barbara L., Saper, Clifford B., Schulze-Bonhage, Andreas, Gaillard, William D.

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals von Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.

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ILAE Genetics Literacy series: Progressive myoclonus epilepsies von Cameron, Jillian M, Ellis, Colin A, Berkovic, Samuel F

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The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures von Burgess, Rosemary, Wang, Shuyu, McTague, Amy, Boysen, Katja E., Yang, Xiaoling, Zeng, Qi, Myers, Kenneth A., Rochtus, Anne, Trivisano, Marina, Gill, Deepak, Sadleir, Lynette G., Specchio, Nicola, Guerrini, Renzo, Marini, Carla, Zhang, Yue‐Hua, Mefford, Heather C., Kurian, Manju A., Poduri, Annapurna H., Scheffer, Ingrid E.

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Polygenic burden in focal and generalized epilepsies von Leu, Costin, Stevelink, Remi, Smith, Alexander W, Goleva, Slavina B, Kanai, Masahiro, Ferguson, Lisa, Campbell, Ciaran, Kamatani, Yoichiro, Okada, Yukinori, Sisodiya, Sanjay M, Cavalleri, Gianpiero L, Koeleman, Bobby P C, Lerche, Holger, Jehi, Lara, Davis, Lea K, Najm, Imad M, Palotie, Aarno, Daly, Mark J, Busch, Robyn M, Lal, Dennis

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De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder von Sleyp, Yoeri, Valenzuela, Irene, Accogli, Andrea, Ballon, Katleen, Ben-Zeev, Bruria, Berkovic, Samuel F., Broly, Martin, Callaerts, Patrick, Caylor, Raymond C., Charles, Perrine, Chatron, Nicolas, Cohen, Lior, Coppola, Antonietta, Cordeiro, Dawn, Cuccurullo, Claudia, Cuscó, Ivon, Janette diMonda, Duran-Romaña, Ramon, Ekhilevitch, Nina, Fernández-Alvarez, Paula, Gordon, Christopher T., Isidor, Bertrand, Keren, Boris, Lesca, Gaetan, Maljaars, Jarymke, Mercimek-Andrews, Saadet, Morrow, Michelle M., Muir, Alison M., Rousseau, Frederic, Salpietro, Vincenzo, Scheffer, Ingrid E., Schnur, Rhonda E., Schymkowitz, Joost, Souche, Erika, Steyaert, Jean, Stolerman, Elliot S., Vengoechea, Jaime, Ville, Dorothée, Washington, Camerun, Weiss, Karin, Zaid, Rinat, Sadleir, Lynette G., Mefford, Heather C., Peeters, Hilde

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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals von Povysil, Gundula, Allen, Andrew S., Howrigan, Daniel P., Tashman, Katherine, Cerrato, Felecia, Cusick, Caroline, Heyne, Henrike, Churchhouse, Claire, Watts, Nick, Lal, Dennis, Gupta, Namrata, Cavalleri, Gianpiero L., Hakonarson, Hakon, Marson, Anthony G., Petrovski, Slavé, Sisodiya, Sanjay M., Depondt, Chantal, Scheffer, Ingrid E., Krause, Roland, Regan, Brigid M., Leu, Costin, Leech, Stephanie L., Todaro, Marian, Stamberger, Hannah, Kousiappa, Ioanna, Tanteles, George A., Christou, Yiolanda, Laššuthová, Petra, Knake, Susanne, Kunz, Wolfram S., Zsurka, Gábor, Surges, Rainer, Rademacher, Annika, von Spiczak, Sarah, Kanaan, Moien, Canavati, Christina, Lemke, Johannes R., Krey, Ilona, Weber, Yvonne G., Wolking, Stefan, Kegele, Josua, Borggräfe, Ingo, Mayer, Thomas, Brockmann, Knut, Madeleyn, Rene, Saarela, Anni, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Derambure, Philippe, Hirsch, Edouard, Chassoux, Francine, Chung, Seo-Kyung, Schneider, Natascha, Balestrini, Simona, Zagaglia, Sara, Johnson, Michael R., Auce, Pauls, Barišić, Nina, Canafoglia, Laura, Franceschetti, Silvana, Castellotti, Barbara, Granata, Tiziana, Ragona, Francesca, Iacomino, Michele, Riva, Antonella, Vari, Maria Stella, Salpietro, Vincenzo, Mancardi, Maria Margherita, Nobili, Lino, Bisulli, Francesca, Pippucci, Tommaso, Licchetta, Laura, Tinuper, Paolo, Gambardella, Antonio, Labate, Angelo, Annesi, Grazia, Manna, Lorella, Parrini, Elena, Bianchini, Claudia, Montomoli, Martino, Hirose, Shinichi, Yamakawa, Kazuhiro, Beydoun, Ahmad, Sadleir, Lynette G., Topaloglu, Pınar, Baykan, Betül, Özkara, YeşÇiğdem, Ho, Chen-Jui, Chou, I-Jun, Shain, Catherine, Goldman, Alicia, Busch, Robyn M., Jehi, Lara, Ferguson, Lisa, Clark, Peggy O., Privitera, Michael, Schachter, Steven, Cosico, Mahgenn, Lowenstein, Daniel H., Goldstein, David B.

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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects von Niestroj, Lisa-Marie, Perez-Palma, Eduardo, Howrigan, Daniel P, Zhou, Yadi, Cheng, Feixiong, Saarentaus, Elmo, Nürnberg, Peter, Stevelink, Remi, Daly, Mark J, Palotie, Aarno, Lal, Dennis

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A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy von Speed, Doug, Hoggart, Clive, Petrovski, Slave, Tachmazidou, Ioanna, Coffey, Alison, Jorgensen, Andrea, Eleftherohorinou, Hariklia, De Iorio, Maria, Todaro, Marian, De, Tisham, Smith, David, Smith, Philip E, Jackson, Margaret, Cooper, Paul, Kellett, Mark, Howell, Stephen, Newton, Mark, Yerra, Raju, Tan, Meng, French, Chris, Reuber, Markus, Sills, Graeme E, Chadwick, David, Pirmohamed, Munir, Bentley, David, Scheffer, Ingrid, Berkovic, Samuel, Balding, David, Palotie, Aarno, Marson, Anthony, O'Brien, Terence J, Johnson, Michael R

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De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder von Sleyp, Yoeri, Valenzuela, Irene, Accogli, Andrea, Ballon, Katleen, Ben-Zeev, Bruria, Berkovic, Samuel F, Broly, Martin, Callaerts, Patrick, Caylor, Raymond C, Charles, Perrine, Chatron, Nicolas, Cohen, Lior, Coppola, Antonietta, Cordeiro, Dawn, Cuccurullo, Claudia, Cusco, Ivon, Duran-Romana, Ramon, Ekhilevitch, Nina, Fernandez-Alvarez, Paula, Gordon, Christopher T, Isidor, Bertrand, Keren, Boris, Lesca, Gaetan, Maljaars, Jarymke, Mercimek-Andrews, Saadet, Morrow, Michelle M, Muir, Alison M, Rousseau, Frederic, Salpietro, Vincenzo, Scheffer, Ingrid E, Schnur, Rhonda E, Schymkowitz, Joost, Souche, Erika, Steyaert, Jean, Stolerman, Elliot S, Vengoechea, Jaime, Ville, Dorothee, Washington, Camerun, Weiss, Karin, Zaid, Rinat, Sadleir, Lynette G, Mefford, Heather C, Peeters, Hilde

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Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females von D’Agostino, Maria Daniela, Bernasconi, Andrea, Das, Soma, Bastos, Alexandre, Valerio, Rosa M., Palmini, André, Costa da Costa, Jaderson, Scheffer, Ingrid E., Berkovic, Samuel, Guerrini, Renzo, Dravet, Charlotte, Ono, Jiro, Gigli, GianLuigi, Federico, Antonio, Booth, Fran, Bernardi, Bruno, Volpi, Lilia, Tassinari, Carlo Alberto, Guggenheim, Mary Anne, Ledbetter, David H., Gleeson, Joseph G., Lopes‐Cendes, Iscia, Vossler, David G., Malaspina, Elisabetta, Franzoni, Emilio, Sartori, Roberto J., Mitchell, Michael H., Mercho, Suha, Dubeau, François, Andermann, Frederick, Dobyns, William B., Andermann, Eva

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