X-ray Crystallographic and Mössbauer Spectroscopic Applications in Dependence of Partial Quadrupole Splitting, [R], on the C−Sn−C Angle in Seven-Coordinated Diorganotin(IV) Complex... von de Sousa, Gerimário F, Deflon, Victor M, Gambardella, Maria T. do P, Francisco, Regina H. P, Ardisson, José D, Niquet, Elke

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New Heptacoordinated Organotin(IV) Complexes Derivatives of 2,6-diacetylpyridinebis(2-furanoylhydrazone), H2dapf, and 2,6-diacetylpyridinebis(2-thenoylhydrazone), H2dapt: Crystal a... von Sousa, Gerimário F. de, Mangas, Maria B.P., Francisco, Regina H.P., Gambardella, Maria T. do P., Rodrigues, Ana M.G.D., Abras, Anuar

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Rhodium carboxylate complexes of diphenyltriazene and berenil, a substituted triazene and DNA binding ligand. Crystal and molecular structure of tetrakis(.mu.-acetato)bis(diphenylt... von Farrell, Nicholas, Vargas, Maria D, Mascarenhas, Yvonne A, Gambardella, Maria T. do P

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Preparation, X-ray structural studies and plant growth regulatory activity of methyl 6alpha,7beta-thiocarbonyldioxyvouacapan-17 beta-oate von Rubinger, Mayura M. M., Castelo-Branco, Pedro de A., Guilardi, Silvana, Souza, Elysângela M. R., Gambardella, Maria T. do P., Borges, Eduardo E. L., Ferreira-Alves, Dalton L., Piló-Veloso, Dorila

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Preparation, X-ray structural studies and plant growth regulatory activity of methyl 6a,7b-thiocarbonyldioxyvouacapan-17 b-oate von Rubinger Mayura M. M., Castelo-Branco Pedro de A., Guilardi Silvana, Souza Elysângela M. R., Gambardella Maria T. do P., Borges Eduardo E. L., Ferreira-Alves Dalton L., Piló-Veloso Dorila

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Activation of Carbon Dioxide by Bicyclic Amidines von Pérez, Eduardo R, Santos, Regina H. A, Gambardella, Maria T. P, de Macedo, Luiz G. M, Rodrigues-Filho, Ubirajara P, Launay, Jean-Claude, Franco, Douglas W

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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis von Johnson, Janel O, Pioro, Erik P, Boehringer, Ashley, Chia, Ruth, Feit, Howard, Renton, Alan E, Pliner, Hannah A, Abramzon, Yevgeniya, Marangi, Giuseppe, Winborn, Brett J, Gibbs, J Raphael, Nalls, Michael A, Morgan, Sarah, Shoai, Maryam, Hardy, John, Pittman, Alan, Orrell, Richard W, Malaspina, Andrea, Sidle, Katie C, Fratta, Pietro, Harms, Matthew B, Baloh, Robert H, Pestronk, Alan, Weihl, Conrad C, Rogaeva, Ekaterina, Zinman, Lorne, Drory, Vivian E, Borghero, Giuseppe, Mora, Gabriele, Calvo, Andrea, Rothstein, Jeffrey D, Drepper, Carsten, Sendtner, Michael, Singleton, Andrew B, Taylor, J Paul, Cookson, Mark R, Restagno, Gabriella, Sabatelli, Mario, Bowser, Robert, Chiò, Adriano, Traynor, Bryan J

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Crowdsourcing the creation of image segmentation algorithms for connectomics von Arganda-Carreras, Ignacio, Turaga, Srinivas C, Berger, Daniel R, Cireşan, Dan, Giusti, Alessandro, Gambardella, Luca M, Schmidhuber, Jürgen, Laptev, Dmitry, Dwivedi, Sarvesh, Buhmann, Joachim M, Liu, Ting, Seyedhosseini, Mojtaba, Tasdizen, Tolga, Kamentsky, Lee, Burget, Radim, Uher, Vaclav, Tan, Xiao, Sun, Changming, Pham, Tuan D, Bas, Erhan, Uzunbas, Mustafa G, Cardona, Albert, Schindelin, Johannes, Seung, H Sebastian

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Ataxin-1 and ataxin-2 intermediate-length PolyQ expansions in amyotrophic lateral sclerosis von CONFORTI, Francesca L, SPATARO, Rossella, MUGLIA, Maria, RODOLICO, Carmelo, VALENTINO, Paola, BONO, Francesco, COLLETTI, Tiziana, MONSURRO, Maria R, GAMBARDELLA, Antonio, LA BELLA, Vincenzo, SPROVIERO, William, MAZZEI, Rosalucia, CAVALCANTI, Francesca, CONDINO, Francesca, SIMONE, Isabella L, LOGROSCINO, Giancarlo, PATITUCCI, Alessandra, MAGARIELLO, Angela

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AntHocNet: An Ant-Based Hybrid Routing Algorithm for Mobile Ad Hoc Networks von Di Caro, Gianni, Ducatelle, Frederick, Gambardella, Luca Maria

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Genetic counselling in ALS: facts, uncertainties and clinical suggestions von Chiò, Adriano, Battistini, Stefania, Calvo, Andrea, Caponnetto, Claudia, Conforti, Francesca L, Corbo, Massimo, Giannini, Fabio, Mandrioli, Jessica, Mora, Gabriele, Sabatelli, Mario, Ajmone, Clara, Mastro, Enza, Pain, Debora, Mandich, Paola, Penco, Silvana, Restagno, Gabriella, Zollino, Marcella, Surbone, Antonella

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Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 von Bolino, Alessandra, Muglia, Maria, Conforti, Francesca Luisa, LeGuern, Eric, Salih, Mustafa A.M., Georgiou, Domna-Maria, Christodoulou, Kyproula, Hausmanowa-Petrusewicz, Irena, Mandich, Paola, Schenone, Angelo, Gambardella, Antonio, Bono, Franco, Quattrone, Aldo, Devoto, Marcella, Monaco, Anthony P.

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Risk of Major Congenital Malformations and Exposure to Antiseizure Medication Monotherapy von Battino, Dina, Tomson, Torbjörn, Bonizzoni, Erminio, Craig, John, Perucca, Emilio, Sabers, Anne, Thomas, Sanjeev, Alvestad, Silje, Perucca, Piero, Vajda, Frank

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Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72 von CHIO, Adriano, BORGHERO, Giuseppe, PUGLIATTI, Maura, SOTGIU, Maria Alessandra, MURRU, Maria Rita, MARROSU, Maria Giovanna, MARROSU, Francesco, MARINOU, Kalliopi, MANDRIOLI, Jessica, SOLA, Patrizia, CAPONNETTO, Claudia, MANCARDI, Gianluigi, RESTAGNO, Gabriella, MANDICH, Paola, BELLA, Vincenzo La, SPATARO, Rossella, CONTE, Amelia, MONSURRO, Maria Rosaria, TEDESCHI, Gioacchino, PISANO, Fabrizio, BARTOLOMEI, Ilaria, SALVI, Fabrizio, PINTER, Giuseppe Lauria, MORA, Gabriele, SIMONE, Isabella, LOGROSCINO, Giancarlo, GAMBARDELLA, Antonio, QUATTRONE, Aldo, LUNETTA, Christian, VOLANTI, Paolo, ZOLLINO, Marcella, PENCO, Silvana, BATTISTINI, Stefania, RENTON, Alan E, DREPPER, Carsten, MAJOUNIE, Elisa, ABRAMZON, Yevgeniya, CONFORTI, Francesca Luisa, GIANNINI, Fabio, CORBO, Massimo, SABATELLI, Mario, TRAYNOR, Bryan J, SENDTNER, Michael, BRUNETTI, Maura, OSSOLA, Irene, CALVO, Andrea

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Atlas of lesion locations and postsurgical seizure freedom in focal cortical dysplasia: A MELD study von Wagstyl, Konrad, Whitaker, Kirstie, Raznahan, Armin, Seidlitz, Jakob, Vértes, Petra E., Foldes, Stephen, Humphreys, Zachary, Hu, Wenhan, Mo, Jiajie, Likeman, Marcus, Davies, Shirin, Lenge, Matteo, Cohen, Nathan T., Tang, Yingying, Wang, Shan, Ripart, Mathilde, Chari, Aswin, Tisdall, Martin, Bargallo, Nuria, Conde‐Blanco, Estefanía, Pariente, Jose Carlos, Pascual‐Diaz, Saül, Delgado‐Martínez, Ignacio, Pérez‐Enríquez, Carmen, Lagorio, Ilaria, Abela, Eugenio, Mullatti, Nandini, O'Muircheartaigh, Jonathan, Vecchiato, Katy, Liu, Yawu, Caligiuri, Maria, Sinclair, Ben, Vivash, Lucy, Willard, Anna, Kandasamy, Jothy, McLellan, Ailsa, Sokol, Drahoslav, Semmelroch, Mira, Kloster, Ane, Opheim, Giske, Yasuda, Clarissa, Zhang, Kai, Hamandi, Khalid, Barba, Carmen, Guerrini, Renzo, Gaillard, William Davis, You, Xiaozhen, Wang, Irene, González‐Ortiz, Sofía, Severino, Mariasavina, Striano, Pasquale, Tortora, Domenico, Kalviainen, Reetta, Gambardella, Antonio, Labate, Angelo, Desmond, Patricia, Lui, Elaine, O'Brien, Terry, Shetty, Jay, Jackson, Graeme, Duncan, John S., Winston, Gavin P., Pinborg, Lars, Cendes, Fernando, Cross, Judith Helen, Baldeweg, Torsten, Adler, Sophie

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Synthesis of Polyalkylated Indoles Using a Thallium(III)-Mediated Ring-Contraction Reaction von Silva Jr, Luiz F., Craveiro, Marcus V., Gambardella, Maria T.

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Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients von Panagiotakaki, Eleni, De Grandis, Elisa, Stagnaro, Michela, Heinzen, Erin L, Fons, Carmen, Sisodiya, Sanjay, de Vries, Boukje, Goubau, Christophe, Weckhuysen, Sarah, Kemlink, David, Scheffer, Ingrid, Lesca, Gaëtan, Rabilloud, Muriel, Klich, Amna, Ramirez-Camacho, Alia, Ulate-Campos, Adriana, Campistol, Jaume, Giannotta, Melania, Moutard, Marie-Laure, Doummar, Diane, Hubsch-Bonneaud, Cecile, Jaffer, Fatima, Cross, Helen, Gurrieri, Fiorella, Tiziano, Danilo, Nevsimalova, Sona, Nicole, Sophie, Neville, Brian, van den Maagdenberg, Arn M J M, Mikati, Mohamad, Goldstein, David B, Vavassori, Rosaria, Arzimanoglou, Alexis

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Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study von Larivière, Sara, Rodríguez-Cruces, Raúl, Royer, Jessica, Caligiuri, Maria Eugenia, Gambardella, Antonio, Concha, Luis, Keller, Simon S, Cendes, Fernando, Yasuda, Clarissa, Bonilha, Leonardo, Gleichgerrcht, Ezequiel, Focke, Niels K, Domin, Martin, von Podewills, Felix, Langner, Soenke, Rummel, Christian, Wiest, Roland, Martin, Pascal, Kotikalapudi, Raviteja, O'Brien, Terence J, Sinclair, Benjamin, Vivash, Lucy, Desmond, Patricia M, Alhusaini, Saud, Doherty, Colin P, Cavalleri, Gianpiero L, Delanty, Norman, Kälviäinen, Reetta, Jackson, Graeme D, Kowalczyk, Magdalena, Mascalchi, Mario, Semmelroch, Mira, Thomas, Rhys H, Soltanian-Zadeh, Hamid, Davoodi-Bojd, Esmaeil, Zhang, Junsong, Lenge, Matteo, Guerrini, Renzo, Bartolini, Emanuele, Hamandi, Khalid, Foley, Sonya, Weber, Bernd, Depondt, Chantal, Absil, Julie, Carr, Sarah J A, Abela, Eugenio, Richardson, Mark P, Devinsky, Orrin, Severino, Mariasavina, Striano, Pasquale, Tortora, Domenico, Hatton, Sean N, Vos, Sjoerd B, Duncan, John S, Whelan, Christopher D, Thompson, Paul M, Sisodiya, Sanjay M, Bernasconi, Andrea, Labate, Angelo, McDonald, Carrie R, Bernasconi, Neda, Bernhardt, Boris C

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Patterns of subregional cerebellar atrophy across epilepsy syndromes: An ENIGMA‐Epilepsy study von Kerestes, Rebecca, Perry, Andrew, Vivash, Lucy, O'Brien, Terence J., Alvim, Marina K. M., Arienzo, Donatello, Aventurato, Ítalo K., Ballerini, Alice, Baltazar, Gabriel F., Bargalló, Núria, Bender, Benjamin, Brioschi, Ricardo, Bürkle, Eva, Caligiuri, Maria Eugenia, Cendes, Fernando, Tisi, Jane, Duncan, John S., Engel, Jerome P., Foley, Sonya, Fortunato, Francesco, Gambardella, Antonio, Giacomini, Thea, Guerrini, Renzo, Hall, Gerard, Hamandi, Khalid, Ives‐Deliperi, Victoria, João, Rafael B., Keller, Simon S., Kleiser, Benedict, Labate, Angelo, Lenge, Matteo, Marotta, Cassandra, Martin, Pascal, Mascalchi, Mario, Meletti, Stefano, Owens‐Walton, Conor, Parodi, Costanza B., Pascual‐Diaz, Saül, Powell, David, Rao, Jun, Rebsamen, Michael, Reiter, Johannes, Riva, Antonella, Rüber, Theodor, Rummel, Christian, Scheffler, Freda, Severino, Mariasavina, Silva, Lucas S., Staba, Richard J., Stein, Dan J., Striano, Pasquale, Taylor, Peter N., Thomopoulos, Sophia I., Thompson, Paul M., Tortora, Domenico, Vaudano, Anna Elisabetta, Weber, Bernd, Wiest, Roland, Winston, Gavin P., Yasuda, Clarissa L., Zheng, Hong, McDonald, Carrie R., Sisodiya, Sanjay M., Harding, Ian H.

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A Common Polymorphism in the Promoter of UCP2 Contributes to the Variation in Insulin Secretion in Glucose-Tolerant Subjects von SESTI, Giorgio, CARDELLINI, Marina, GAMBARDELLA, Sergio, FEDERICI, Massimo, MARCHETTI, Piero, LAURO, Renato, MARINI, Maria Adelaide, FRONTONI, Simona, D'ADAMO, Monica, DEL GUERRA, Silvia, LAURO, Davide, DE NICOLAIS, Pierluigi, SBRACCIA, Paolo, DEL PRATO, Stefano

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