Horizontal vs vertical. The public space in section von Filippo Orsini, Pasquale Mei

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Orizzontale vs verticale. Lo spazio pubblico in sezione von Orsini, Filippo, Mei, Pasquale

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Sensing Dynamic Forces by Fe-Ga in Compression von Zucca, Mauro, Mei, Pasquale, Ferrara, Enzo, Fiorillo, Fausto

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Polymeric Composite Foams With Properties Controlled by the Magnetic Field von Davino, Daniele, Mei, Pasquale, Sorrentino, Luigi, Visone, Ciro

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Mimicking the Anisotropic Behavior of Natural Porous Structures by Controlling the Reinforcing Particles Distribution in Polymeric Foams von Davino, Daniele, D'Auria, Marco, Mei, Pasquale, Iannace, Salvatore, Sorrentino, Luigi, Visone, Ciro, Aurilia, Marco

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SUPPORT DEVICE FOR AN INDUCTION COIL von VIROLI, Alex, MEI, Pasquale, MENGOZZI, Alan, MILANESI, Filippo, NOSTRO, Massimo, URGESE, Emanuel, CORSI, Giacomo, ZANGOLI, Massimo

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SUPPORT DEVICE FOR AN INDUCTION COIL von VIROLI, Alex, MEI, Pasquale, MENGOZZI, Alan, MILANESI, Filippo, NOSTRO, Massimo, URGESE, Emanuel, CORSI, Giacomo, ZANGOLI, Massimo

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Insight into Crosstalk between Ferroptosis and Necroptosis: Novel Therapeutics in Ischemic Stroke von Zhou, Yue, Liao, Jun, Mei, Zhigang, Liu, Xun, Ge, Jinwen

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Dynamin-Related Protein 1 Is Involved in Mitochondrial Damage, Defective Mitophagy, and NLRP3 Inflammasome Activation Induced by MSU Crystals von Jiang, Hui, Chen, Feng, Song, DianZe, Zhou, Xiaoqin, Ren, Long, Zeng, Mei

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Hidden Markov models for monitoring circadian rhythmicity in telemetric activity data von Huang, Qi, Cohen, Dwayne, Komarzynski, Sandra, Li, Xiao-Mei, Innominato, Pasquale, Lévi, Francis, Finkenstädt, Bärbel

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Exosomes Derived From Schwann Cells Ameliorate Peripheral Neuropathy in Type 2 Diabetic Mice von Wang, Lei, Chopp, Michael, Szalad, Alexandra, Lu, XueRong, Zhang, Yi, Wang, Xinli, Cepparulo, Pasquale, Lu, Mei, Li, Chao, Zhang, Zheng Gang

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Mortality and Disease Burden of Injuries from 2008 to 2017 in Anhui Province, China von Zhao, Chan-Na, Wu, Qian, Pan, Hai-Feng, Liu, Zhi-Rong, Hu, Wenbiao, Mao, Yan-Mei, Liu, Li-Na, Chen, Ye-Ji, Li, Rui, He, Qin, Xu, Zhiwei, Wang, Peng, Xing, Xiu-Ya, Dan, Yi-Lin

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MicroRNA-210 as a Novel Therapy for Treatment of Ischemic Heart Disease von SHIJUN HU, MEI HUANG, ROBBINS, Robert C, WU, Joseph C, ZONGJIN LI, FANGJUN JIA, ZHUMUR GHOSH, LIJKWAN, Maarten A, FASANARO, Pasquale, NING SUN, XI WANG, MARTELLI, Fabio

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Exploration for native parasitoids of Drosophila suzukii in China reveals a diversity of parasitoid species and narrow host range of the dominant parasitoid von Giorgini, Massimo, Wang, Xin-Geng, Wang, Yan, Chen, Fu-Shou, Hougardy, Evelyne, Zhang, Hong-Mei, Chen, Zong-Qi, Chen, Hong-Yin, Liu, Chen-Xi, Cascone, Pasquale, Formisano, Giorgio, Carvalho, Gislaine A., Biondi, Antonio, Buffington, Matthew, Daane, Kent M., Hoelmer, Kim A., Guerrieri, Emilio

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Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3 von Florian, Rahel T., Kraft, Florian, Leitão, Elsa, Kaya, Sabine, Klebe, Stephan, Magnin, Eloi, van Rootselaar, Anne-Fleur, Buratti, Julien, Kühnel, Theresa, Schröder, Christopher, Giesselmann, Sebastian, Tschernoster, Nikolai, Altmueller, Janine, Lamiral, Anaide, Keren, Boris, Nava, Caroline, Bouteiller, Delphine, Forlani, Sylvie, Jornea, Ludmila, Kubica, Regina, Ye, Tao, Plassard, Damien, Jost, Bernard, Meyer, Vincent, Deleuze, Jean-François, Delpu, Yannick, Avarello, Mario D. M., Vijfhuizen, Lisanne S., Rudolf, Gabrielle, Hirsch, Edouard, Kroes, Thessa, Reif, Philipp S., Rosenow, Felix, Ganos, Christos, Vidailhet, Marie, Thivard, Lionel, Mathieu, Alexandre, Bourgeron, Thomas, Kurth, Ingo, Rafehi, Haloom, Steenpass, Laura, Horsthemke, Bernhard, LeGuern, Eric, Klein, Karl Martin, Labauge, Pierre, Bennett, Mark F., Bahlo, Melanie, Gecz, Jozef, Corbett, Mark A., Tijssen, Marina A. J., van den Maagdenberg, Arn M. J. M., Depienne, Christel

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Defining the electroclinical phenotype and outcome of PCDH19‐related epilepsy: A multicenter study von Trivisano, Marina, Pietrafusa, Nicola, Terracciano, Alessandra, Marini, Carla, Mei, Davide, Darra, Francesca, Accorsi, Patrizia, Battaglia, Domenica, Caffi, Lorella, Canevini, Maria P., Cappelletti, Simona, Cesaroni, Elisabetta, Palma, Luca, Costa, Paola, Cusmai, Raffaella, Giordano, Lucio, Ferrari, Annarita, Freri, Elena, Fusco, Lucia, Granata, Tiziana, Martino, Tommaso, Mastrangelo, Massimo, Bova, Stefania M., Parmeggiani, Lucio, Ragona, Francesca, Sicca, Federico, Striano, Pasquale, Specchio, Luigi M., Tondo, Ilaria, Zambrelli, Elena, Zamponi, Nelia, Zanus, Caterina, Boniver, Clementina, Vecchi, Marilena, Avolio, Carlo, Dalla Bernardina, Bernardo, Bertini, Enrico, Guerrini, Renzo, Vigevano, Federico, Specchio, Nicola

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Morphometric network-based abnormalities correlate with psychiatric comorbidities and gene expression in PCDH19-related developmental and epileptic encephalopathy von Lenge, Matteo, Balestrini, Simona, Napolitano, Antonio, Mei, Davide, Conti, Valerio, Baldassarri, Giulia, Trivisano, Marina, Pellacani, Simona, Macconi, Letizia, Longo, Daniela, Rossi Espagnet, Maria Camilla, Cappelletti, Simona, D’Incerti, Ludovico, Barba, Carmen, Specchio, Nicola, Guerrini, Renzo

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Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 von Corbett, Mark A., Kroes, Thessa, Veneziano, Liana, Bennett, Mark F., Florian, Rahel, Schneider, Amy L., Coppola, Antonietta, Licchetta, Laura, Franceschetti, Silvana, Suppa, Antonio, Wenger, Aaron, Mei, Davide, Pendziwiat, Manuela, Kaya, Sabine, Delledonne, Massimo, Straussberg, Rachel, Xumerle, Luciano, Regan, Brigid, Crompton, Douglas, van Rootselaar, Anne-Fleur, Correll, Anthony, Catford, Rachael, Bisulli, Francesca, Chakraborty, Shreyasee, Baldassari, Sara, Tinuper, Paolo, Barton, Kirston, Carswell, Shaun, Smith, Martin, Berardelli, Alfredo, Carroll, Renee, Gardner, Alison, Friend, Kathryn L., Blatt, Ilan, Iacomino, Michele, Di Bonaventura, Carlo, Striano, Salvatore, Buratti, Julien, Keren, Boris, Nava, Caroline, Forlani, Sylvie, Rudolf, Gabrielle, Hirsch, Edouard, Leguern, Eric, Labauge, Pierre, Balestrini, Simona, Sander, Josemir W., Afawi, Zaid, Helbig, Ingo, Ishiura, Hiroyuki, Tsuji, Shoji, Sisodiya, Sanjay M., Casari, Giorgio, Sadleir, Lynette G., van Coller, Riaan, Tijssen, Marina A. J., Klein, Karl Martin, van den Maagdenberg, Arn M. J. M., Zara, Federico, Guerrini, Renzo, Berkovic, Samuel F., Pippucci, Tommaso, Canafoglia, Laura, Bahlo, Melanie, Striano, Pasquale, Scheffer, Ingrid E., Brancati, Francesco, Depienne, Christel, Gecz, Jozef

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Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma von Hysi, Pirro G, Cheng, Ching-Yu, Springelkamp, Henriët, Macgregor, Stuart, Bailey, Jessica N Cooke, Wojciechowski, Robert, Vitart, Veronique, Nag, Abhishek, Hewitt, Alex W, Höhn, René, Venturini, Cristina, Mirshahi, Alireza, Ramdas, Wishal D, Thorleifsson, Gudmar, Vithana, Eranga, Khor, Chiea-Chuen, Stefansson, Arni B, Liao, Jiemin, Haines, Jonathan L, Amin, Najaf, Wang, Ya Xing, Wild, Philipp S, Ozel, Ayse B, Li, Jun Z, Fleck, Brian W, Zeller, Tanja, Staffieri, Sandra E, Teo, Yik-Ying, Cuellar-Partida, Gabriel, Luo, Xiaoyan, Allingham, R Rand, Richards, Julia E, Senft, Andrea, Karssen, Lennart C, Zheng, Yingfeng, Bellenguez, Céline, Xu, Liang, Iglesias, Adriana I, Wilson, James F, Kang, Jae H, van Leeuwen, Elisabeth M, Jonsson, Vesteinn, Thorsteinsdottir, Unnur, Despriet, Dominiek D G, Ennis, Sarah, Moroi, Sayoko E, Martin, Nicholas G, Jansonius, Nomdo M, Yazar, Seyhan, Tai, E-Shyong, Amouyel, Philippe, Kirwan, James, van Koolwijk, Leonieke M E, Hauser, Michael A, Jonasson, Fridbert, Leo, Paul, Loomis, Stephanie J, Fogarty, Rhys, Rivadeneira, Fernando, Kearns, Lisa, Lackner, Karl J, de Jong, Paulus T V M, Simpson, Claire L, Pennell, Craig E, Oostra, Ben A, Uitterlinden, André G, Saw, Seang-Mei, Lotery, Andrew J, Bailey-Wilson, Joan E, Hofman, Albert, Vingerling, Johannes R, Maubaret, Cécilia, Pfeiffer, Norbert, Wolfs, Roger C W, Lemij, Hans G, Young, Terri L, Pasquale, Louis R, Delcourt, Cécile, Spector, Timothy D, Klaver, Caroline C W, Small, Kerrin S, Burdon, Kathryn P, Stefansson, Kari, Wong, Tien-Yin, Viswanathan, Ananth, Mackey, David A, Craig, Jamie E, Wiggs, Janey L, van Duijn, Cornelia M, Hammond, Christopher J, Aung, Tin

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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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