GAGLIARDI, MONICA

GAGLIARDI, MONICA  

Istituto di Bioimmagini e Sistemi Biologici Complessi (IBSBC) - Sede Secondaria di Germaneto (CZ)  

Mostra records
Risultati 1 - 20 di 21 (tempo di esecuzione: 0.033 secondi).
Titolo Data di pubblicazione Autore(i) File
USP25 in genetic generalized epilepsy: a gene under scrutiny 1-gen-2025 Maryam, Erfanian Omidvar; Jill R, Murrell; Anna J, Prentice; Ingo, Helbig; Holger, Lerche; Patrick, May; Chen, Siwei; Afawi, Zaid; Zulfiqar Ali, Quratulain; Amadori, Elisabetta; Anderson, Alison; Andrade, Danielle 4 M.; Annesi, Grazia; Balagura, Ganna; Balestrini, Simona; Barba, Carmen; Baum, Larry W.; Baumgartner, 5 Tobias H.; Baykan, Betül; Becker, Felicitas; Bennett, Caitlin A.; Beydoun, Ahmad; Francesca Bisulli, 6; Borggräfe, Ingo; Bosselmann, Christian; Buono, Russell J.; Busch, Robyn M.; Laura Canafoglia, 7; Castellotti, Barbara; Cavalleri, Gianpiero L.; Cerrato, Felecia; Chou, I-Jun; 8 Kyung Chung, Seo-; Cole, Andrew J.; Cossette, Patrick; Cotsapas, Chris; Depondt, Chantal; 9 Devinsky, Orrin; Dlugos, Dennis J.; Doccini, Viola; Ellis, Colin; Epstein, Leon; Evans, Meghan; 10 Faucon, Annika; Ferguson, Lisa; Ferraro, Thomas N.; Feucht, Martha; Fitzgerald, Mark; Fortunato, Francesco; French, 11 Jacqueline A.; Freri, Elena; Gagliardi, Monica; Goldman, Alica; Goldstein, David B.; 12 Granata, Tiziana; Guerrini, Renzo; Haas, Kevin; Heinzen, Erin L.; Helbig, Ingo; Heyne, Henrike; 13 Hoeper, Olivia; Midori Inuzuka, Luciana; Jehi, Lara; Kälviäinen, Reetta; Kariuki, Symon M.; Khoury, Jean; Karl Martin Klein, 14; Kluger, Gerhard; Knake, Susanne; Koupparis, Andreas; Kousiappa, Ioanna; Roland Krause, 15; Krenn, Martin; Krestel, Heinz; Kurlemann, Gerhard; Labate, Angelo; Lacey, Austin; Charlotte Lawthom, 16; Leech, Stephanie L.; Lemke, Johannes R.; Lerche, Holger; Lesca, Gaetan; 17 Leu, Costin; Lewis-Smith, David; Liao, Calwing; Licchetta, Laura; Lowenstein, Daniel H.; Madia, Francesca; Stefania Magri, 18; May, Patrick; Mcgraw, Christopher M.; Mei, Davide; Millichap, John J.; 19 Minardi, Raffaella; Muccioli, Lorenzo; Muhle, Hiltrud; Müller-Schlüter, Karen; Nasreddine, Wassim; 20 Neubauer, Bernd A.; Newton, Charles R. J. C.; O'Brien, Terence J.; Özkara, Çiğdem; Papacostas, Savvas S.; Elena Parrini, 21; Pendziwiat, Manuela; Pickrell, William O.; Pinto, Dalila; Poduri, Annapurna; Francesca Ragona, 22; Rees, Mark I.; Rheims, Sylvain; Riva, Antonella; Rojas, Enrique; 23 Sammarra, Ilaria; Schankin, Christoph J.; Scheffer, Ingrid E.; Schubert-Bast, Susanne; Schulze- 24 Bonhage, Andreas; Shiedley, Beth R.; Sisodiya, Sanjay M.; Sparks, Kathryn R.; Stephani, Ulrich; 25 Striano, Pasquale; Strzelczyk, Adam; Surges, Rainer; Suzuki, Toshimitsu; Talarico, Mariagrazia; 26 Talkowski, Michael E.; Tanteles, George A.; Tinuper, Paolo; Todaro, Marian; Topaloglu, Pınar; Tsai, Meng-Han; Birute Tumiene, 27; Turkdogan, Dilsad; Utkus, Algirdas; Valton, Luc; Van Baalen, Andreas; 28 Vetro, Annalisa; Wagner, Ryan G.; Weber, Yvonne G.; Weckhuysen, Sarah; Wiebe, Samuel; Wolking, Stefan; 1093/brain/awaf406/8304399 By Biblioteca Dell Area User On 10 December 2025 Randi Von Wrede, ACCEPTED MANUSCRIPT Downloaded from https://academic. oup. com/brain/advance-article/doi/10.; Yapıcı, Zuhal; Zahnert, Felix; Zara, Federico; Zsurka, Gábor; Neale, 1 Benjamin M.; F. Berkovic., 2 Samuel
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes 1-gen-2024 Null, Null; Chen, Siwei; Abou-Khalil, Bassel W.; Afawi, Zaid; Ali, Quratulain Zulfiqar; Amadori, Elisabetta; Anderson, Alison; Anderson, Joe; Andrade, Danielle M.; Annesi, Grazia; Arslan, Mutluay; Auce, Pauls; Bahlo, Melanie; Baker, Mark D.; Balagura, Ganna; Balestrini, Simona; Banks, Eric; Barba, Carmen; Barboza, Karen; Bartolomei, Fabrice; Bass, Nick; Baum, Larry W.; Baumgartner, Tobias H.; Baykan, Betül; Bebek, Nerses; Becker, Felicitas; Bennett, Caitlin A.; Beydoun, Ahmad; Bianchini, Claudia; Bisulli, Francesca; Blackwood, Douglas; Blatt, Ilan; Borggräfe, Ingo; Bosselmann, Christian; Braatz, Vera; Brand, Harrison; Brockmann, Knut; Buono, Russell J.; Busch, Robyn M.; Caglayan, S. Hande; Canafoglia, Laura; Canavati, Christina; Castellotti, Barbara; Cavalleri, Gianpiero L.; Cerrato, Felecia; Chassoux, Francine; Cherian, Christina; Cherny, Stacey S.; Cheung, Ching-Lung; Chou, I-Jun; Chung, Seo-Kyung; Churchhouse, Claire; Ciullo, Valentina; Clark, Peggy O.; Cole, Andrew J.; Cosico, Mahgenn; Cossette, Patrick; Cotsapas, Chris; Cusick, Caroline; Daly, Mark J.; Davis, Lea K.; Jonghe, Peter De; Delanty, Norman; Dennig, Dieter; Depondt, Chantal; Derambure, Philippe; Devinsky, Orrin; Vito, Lidia Di; Dickerson, Faith; Dlugos, Dennis J.; Doccini, Viola; Doherty, Colin P.; El-Naggar, Hany; Ellis, Colin A.; Epstein, Leon; Evans, Meghan; Faucon, Annika; Feng, Yen-Chen Anne; Ferguson, Lisa; Ferraro, Thomas N.; Silva, Izabela Ferreira Da; Ferri, Lorenzo; Feucht, Martha; Fields, Madeline C.; Fitzgerald, Mark; Fonferko-Shadrach, Beata; Fortunato, Francesco; Franceschetti, Silvana; French, Jacqueline A.; Freri, Elena; Fu, Jack M.; Gabriel, Stacey; Gagliardi, Monica; Gambardella, Antonio; Gauthier, Laura; Giangregorio, Tania; Gili, Tommaso; Glauser, Tracy A.; Goldberg, Ethan; Goldman, Alica; Goldstein, David B.; Granata, Tiziana; Grant, Riley; Greenberg, David A.; Guerrini, Renzo; Gundogdu-Eken, Aslı; Gupta, Namrata; Haas, Kevin; Hakonarson, Hakon; Haryanyan, Garen; Häusler, Martin; Hegde, Manu; Heinzen, Erin L.; Helbig, Ingo; Hengsbach, Christian; Heyne, Henrike; Hirose, Shinichi; Hirsch, Edouard; Ho, Chen-Jui; Hoeper, Olivia; Howrigan, Daniel P.; Hucks, Donald; Hung, Po-Chen; Iacomino, Michele; Inoue, Yushi; Inuzuka, Luciana Midori; Ishii, Atsushi; Jehi, Lara; Johnson, Michael R.; Johnstone, Mandy; Kälviäinen, Reetta; Kanaan, Moien; Kara, Bulent; Kariuki, Symon M.; Kegele, Josua; Kesim, Yeşim; Khoueiry-Zgheib, Nathalie; Khoury, Jean; King, Chontelle; Klein, Karl Martin; Kluger, Gerhard; Knake, Susanne; Kok, Fernando; Korczyn, Amos D.; Korinthenberg, Rudolf; Koupparis, Andreas; Kousiappa, Ioanna; Krause, Roland; Krenn, Martin; Krestel, Heinz; Krey, Ilona; Kunz, Wolfram S.; Kurlemann, Gerhard; Kuzniecky, Ruben I.; Kwan, Patrick; Vega-Talbott, Maite La; Labate, Angelo; Lacey, Austin; Lal, Dennis; Laššuthová, Petra; Lauxmann, Stephan; Lawthom, Charlotte; Leech, Stephanie L.; Lehesjoki, Anna-Elina; Lemke, Johannes R.; Lerche, Holger; Lesca, Gaetan; Leu, Costin; Lewin, Naomi; Lewis-Smith, David; Li, Gloria Hoi-Yee; Liao, Calwing; Licchetta, Laura; Lin, Chih-Hsiang; Lin, Kuang-Lin; Linnankivi, Tarja; Lo, Warren; Lowenstein, Daniel H.; Lowther, Chelsea; Lubbers, Laura; Lui, Colin H. T.; Macedo-Souza, Lucia Inês; Madeleyn, Rene; Madia, Francesca; Magri, Stefania; Maillard, Louis; Marcuse, Lara; Marques, Paula; Marson, Anthony G.; Matthews, Abigail G.; May, Patrick; Mayer, Thomas; Mcardle, Wendy; Mccarroll, Steven M.; Mcgoldrick, Patricia; Mcgraw, Christopher M.; Mcintosh, Andrew; Mcquillan, Andrew; Meador, Kimford J.; Mei, Davide; Michel, Véronique; Millichap, John J.; Minardi, Raffaella; Montomoli, Martino; Mostacci, Barbara; Muccioli, Lorenzo; Muhle, Hiltrud; Müller-Schlüter, Karen; Najm, Imad M.; Nasreddine, Wassim; Neaves, Samuel; Neubauer, Bernd A.; Newton, Charles R. J. C.; Noebels, Jeffrey L.; Northstone, Kate; Novod, Sam; O'Brien, Terence J.; Owusu-Agyei, Seth; Özkara, Çiğdem; Palotie, Aarno; Papacostas, Savvas S.; Parrini, Elena; Pato, Carlos; Pato, Michele; Pendziwiat, Manuela; Pennell, Page B.; Petrovski, Slavé; Pickrell, William O.; Pinsky, Rebecca; Pinto, Dalila; Pippucci, Tommaso; Piras, Fabrizio; Piras, Federica; Poduri, Annapurna; Pondrelli, Federica; Posthuma, Danielle; Powell, Robert H. W.; Privitera, Michael; Rademacher, Annika; Ragona, Francesca; Ramirez-Hamouz, Byron; Rau, Sarah; Raynes, Hillary R.; Rees, Mark I.; Regan, Brigid M.; Reif, Andreas; Reinthaler, Eva; Rheims, Sylvain; Ring, Susan M.; Riva, Antonella; Rojas, Enrique; Rosenow, Felix; Ryvlin, Philippe; Saarela, Anni; Sadleir, Lynette G.; Salman, Barış; Salmon, Andrea; Salpietro, Vincenzo; Sammarra, Ilaria; Scala, Marcello; Schachter, Steven; Schaller, André; Schankin, Christoph J.; Scheffer, Ingrid E.; Schneider, Natascha; Schubert-Bast, Susanne; Schulze-Bonhage, Andreas; Scudieri, Paolo; Sedláčková, Lucie; Shain, Catherine; Sham, Pak C.; Shiedley, Beth R.; Siena, S. Anthony; Sills, Graeme J.; Sisodiya, Sanjay M.; Smoller, Jordan W.; Solomonson, Matthew; Spalletta, Gianfranco; Sparks, Kathryn R.; Sperling, Michael R.; Stamberger, Hannah; Steinhoff, Bernhard J.; Stephani, Ulrich; Štěrbová, Katalin; Stewart, William C.; Stipa, Carlotta; Striano, Pasquale; Strzelczyk, Adam; Surges, Rainer; Suzuki, Toshimitsu; Talarico, Mariagrazia; Talkowski, Michael E.; Taneja, Randip S.; Tanteles, George A.; Timonen, Oskari; Timpson, Nicholas John; Tinuper, Paolo; Todaro, Marian; Topaloglu, Pınar; Tsai, Meng-Han; Tumiene, Birute; Turkdogan, Dilsad; Uğur-İşeri, Sibel; Utkus, Algirdas; Vaidiswaran, Priya; Valton, Luc; van Baalen, Andreas; Vari, Maria Stella; Vetro, Annalisa; Vlčková, Markéta; von Brauchitsch, Sophie; von Spiczak, Sarah; Wagner, Ryan G.; Watts, Nick; Weber, Yvonne G.; Weckhuysen, Sarah; Widdess-Walsh, Peter; Wiebe, Samuel; Wolf, Steven M.; Wolff, Markus; Wolking, Stefan; Wong, Isaac; von Wrede, Randi; Wu, David; Yamakawa, Kazuhiro; Yapıcı, Zuhal; Yis, Uluc; Yolken, Robert; Yücesan, Emrah; Zagaglia, Sara; Zahnert, Felix; Zara, Federico; Zimprich, Fritz; Zizovic, Milena; Zsurka, Gábor; Neale, Benjamin M.; Berkovic, Samuel F.
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia 1-gen-2024 Procopio, Radha; Fortunato, Francesco; Gagliardi, Monica; Talarico, Mariagrazia; Sammarra, Ilaria; Sarubbi, Maria Chiara; Malanga, Donatella; Annesi, Grazia; Gambardella, Antonio
Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study 1-gen-2022 Domenighetti, C; Sugier, Pe; Ashok Kumar Sreelatha, A; Schulte, C; Grover, S; Mohamed, O; Portugal, B; May, P; Bobbili, Dr; Radivojkovblagojevic, M; Lichtner, P; Singleton, Ab; Hernandez, Dg; Edsall, C; Mellick, Gd; Zimprich, A; Pirker, W; Rogaeva, E; Lang, Ae; Koks, S; Taba, P; Lesage, S; Brice, A; Corvol, Jc; Chartierharlin, Mc; Mutez, E; Brockmann, K; Deutschländer, Ab; Hadjigeorgiou, Gm; Dardiotis, E; Stefanis, L; Simitsi, Am; Valente, Em; Petrucci, S; Duga, S; Straniero, L; Zecchinelli, A; Pezzoli, G; Brighina, L; Ferrarese, C; Annesi, G; Quattrone, A; Gagliardi, M; Matsuo, H; Kawamura, Y; Hattori, N; Nishioka, K; Chung, Sj; Kim, Yj; Kolber, P; van de Warrenburg, Bpc; Bloem, Br; Aasly, J; Toft, M; Pihlstrøm, L; Correia Guedes, L; Ferreira JJ Bardien, S; Carr, J; Tolosa, E; Ezquerra, M; Pastor, P; Diezfairen, M; Wirdefeldt, K; Pedersen, Nl; Ran, C; Belin, Ac; Puschmann, A; Hellberg, C; Clarke, Ce; Morrison, Ke; Tan, M; Krainc, D; Burbulla, Lf; Farrer, Mj; Krüger, R; Gasser, T; Sharma, M; Elbaz, A; Comprehensive Unbiased Risk Factor Assessment for, Genetics; Environment in Parkinson's Disease CouragePD, Consortium
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's Disease 1-gen-2022 Cloé Domenighetti; PierreEmmanuel Sugier; Ashwin Ashok Kumar Sreelatha; Claudia Schulte; Sandeep Grover; Océane Mohamed; Berta Portugal; Patrick May; Dheeraj R Bobbili; Milena RadivojkovBlagojevic; Peter Lichtner; Andrew B Singleto; Dena G Hernandez; Connor Edsall; George D Mellick; Alexander Zimprich; Walter Pirker; Ekaterina Rogaeva; Anthony E Lang; Sulev Koks; Pille Taba; Suzanne Lesage; Alexis Brice; JeanChristophe Corvol; MarieChristine ChartierHarlin; Eugénie Mutez; Kathrin Brockmann; Angela B Deutschländer; Georges M Hadjigeorgiou; Efthimos Dardiotis; Leonidas Stefanis; Athina Maria Simitsi; Enza Maria Valente; Simona Petrucci; Stefano Duga; Letizia Straniero; Anna Zecchinelli; Gianni Pezzoli; Laura Brighina; Carlo Ferrarese; Grazia Annesi; Andrea Quattrone; Monica Gagliardi; Hirotaka Matsuo; Yusuke Kawamura; Nobutaka Hattori; Kenya Nishioka; Sun Ju Chung; Yun Joong Kim; Pierre Kolber; Bart Pc van de Warrenburg; Bastiaan R Bloem; Jan Aasly; Mathias Toft; Lasse Pihlstrøm; Leonor Correia Guedes; Joaquim J Ferreira; Soraya Bardien; Jonathan Carr Eduardo Tolosa; Mario Ezquerra; Pau Pastor; Monica DiezFairen; Karin Wirdefeldt; Nancy L Pedersen; Caroline Ran; Andrea C Belin; Andreas Puschmann; Clara Hellberg; Carl E Clarke; Karen E Morrison; Manuela Tan; Dimitri Krainc; Lena F Burbulla; Matt J Farrer; Rejko Krüger; Thomas Gasser; Manu Sharma; Alexis Elbaz; Comprehensive Unbiaised Risk Factor Assessment for Genetics;Environment in Parkinson's Disease CouragePD consortium.
Aceruloplasminemia: A novel splicing mutation preserving the globus pallidus from Iron accumulation 1-gen-2021 Salsone, M; Arabia, G; Annesi, G; Gagliardi, M; Nisticò, R; Novellino, F; Ferinistrambi, L; Quattrone, A; Quattrone, A
Analysis of the LRP10 gene in patients with Parkinson's disease and dementia with Lewy bodies from Southern Italy 1-gen-2021 Gagliardi M.; Procopio R.; Nicoletti G.; Morelli M.; D'Amelio M.; Quattrone A.; Annesi G.
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals 1-gen-2021 E Motelow, Joshua; Povysil, Gundula; S Dhindsa, Ryan; E Stanley, Kate; S Al len, Andrew; Anne Feng, Yenchen; P Howrigan, Daniel; E Abbott, Liam; therine Tashman, Ka; Cerrato, Felecia; Cusick, Caroline; Singh, Tarjinder; Heyne, Henrike; E Byrnes, Andrea; Churchhouse, Claire; Watts, Nick; Solomonson, Matthew; Lal, Dennis; Gupta, Namrata; M Neale, Benjamin; L Cavalleri, Gianpiero; Cossette, Patrick; Cotsapas, Chris; De Jonghe, Peter; Dixonsalazar, Tracy; Guerrini, Renzo; Hakonarson, Hakon; L Heinzen, Erin; Helbig, Ingo; Kwan, Patrick; G Marson, Anthony; Petrovski, Slave; Kamalakaran, Sitharthan; M Sisodiya, Sanjay; Stewart, Randy; Weckhuysen, Sarah; Depondt, Chantal; J Dlugos, Dennis; E Scheffer, Ingrid; Striano, Pasquale; Freyer, Catharine; Krause, Roland; May, Patrick; Mckenna, Kevin; M Regan, Brigid; A Bennett, Caitlin; Leu, Costin; L Leech, Stephanie; J O'Brien, Terence; Todaro, Marian; Stamberger, Hannah; M Andrade, Danielle; Zulfiqar Ali, Quratulain; R Sadoway, Tara; Krestel, Heinz; Schaller, Andre; S Papacostas, Savvas; Kou siappa, Ioanna; A Tanteles, George; Christou, Yiolanda; Sterbova, Katalin; ta Vlckova, Marke; Sedlackova, Lucie; Lassuthova, Petra; Martin Klein, Karl; Rosenow, Felix; S Reif, Philipp; Knake, Susanne; A Neubauer, Bernd; Zimprich, Friedrich; Feucht, Martha; M Reinthaler, Eva; S Kunz, Wolfram; bor Zsurka, Ga; Surges, Rainer; Baumgart ner, Tobias; von Wrede, Randi; Pendziwiat, Manuela; Muhle, Hiltrud; nika Rademacher, An; van Baalen, Andreas; von Spiczak, Sarah; Stephani, Ulrich; Afawi, Zaid; D Korczyn, Amos; Kanaan, Moien; Canavati, Christina; Kurlemann, Gerhard; Mu llerSchlu ter, Karen; Kluger, Gerhard; Ha usler, Martin; Blatt, Ilan; R Lemke, Johannes; Krey, Ilona; G Weber, Yvonne; Wolking, Stefan; Becker, Felicitas; Lauxmann, Stephan; Boßelmann, Christian; Kegele, Josua; Hengs bach, Christian; Rau, Sarah; J Steinhoff, Bernhard; Schulzebonhage, Andreas; Fe, Ingoborggra; Christophjschankin, ; Susanneschubertbast, ; Schreiber, Herbert; Mayer, Thomas; Korinthenberg, Rudolf; Brockmann, Knut; Wolff, Markus; Dennig, Dieter; Madeleyn, Rene; Ka lvia inen, Reetta; Saarela, Anni; Timonen, Oskari; Linnankivi, Tarja; Lehesjoki, Annaelina; Rheims, Sylvain; Lesca, Gaetan; Ryvlin, Philippe; Maillard, Louis; Valton, Luc; Derambure, Philippe; Bartolomei, Fabrice; Hirsch, Edouard; ronique Michel, Ve; Chas soux, Francine; I Rees, Mark; Chung, Seokyung; O Pickrell, William; Powell, Robert; D Baker, Mark; Fonferkoshadrach, Beata; Law thom, Charlotte; Anderson, Joseph; Schneider, Natascha; Balestrini, Simona; Zagaglia, Sara; Braatz, Vera; R Johnson, Michael; Auce, Pauls; J Sills, Graeme; W Baum, Larry; C Sham, Pak; S Cherny, Stacey; HT Lui, Colin; Delanty, Norman; P Doherty, Colin; Shukralla, Arif; Elnaggar, Hany; Widdesswalsh, Peter; Barisic, Nina; The American Journal of Human Genetics, Laura; June, ; cite this article in press as Epi Collaborative, Please; Intolerance, Subgenic; Clinvar, ; A wholeexome sequencing study of, the epilepsies; Individuals, ; American Journal of Human Genetics, The; Httpsdoiorgjajhgcanafoglia, ; Franceschetti, Silvana; Castellotti, Barbara; Granata, Tiziana; Ragona, Francesca; Zara, Federico; Iacomino, Michele; tonella Riva, An; Madia, Francesca; Stella Vari, Maria; Salpie tro, Vincenzo; Scala, Marcello; Margherita Mancardi, Maria; Nobili, Lino; betta Amadori, Elisa; Giacomini, Thea; Bisulli, Francesca; Pippucci, Tommaso; Licchetta, Laura; Minardi, Raffaella; Tinuper, Paolo; enzo Muccioli, Lor; Mostacci, Barbara; Gambardella, Antonio; Labate, Angelo; Annesi, Grazia; Manna, Lorella; Gagliardi, Monica; Parrini, Elena; Mei, Davide; Vetro, Annalisa; Bianchini, Claudia; Montomoli, Martino; Doccini, Viola; Barba, Carmen; Hirose, Shinichi; sushi Ishii, At; Suzuki, Toshimitsu; Inoue, Yushi; Yamakawa, Kazuhiro; Beydoun, Ahmad; Nasreddine, Wassim; Khoueiry Zgheib, Nathalie; Tumiene, Birute; Utkus, Algirdas; G Sadleir, Lynette; King, Chontelle; Hande Caglayan, S; Arslan, Mutluay; Yapc, Zuhal; To paloglu, Pnar; Kara, Bulent; Yis, Uluc; Turkdogan, Dilsad; Gun dogduEken, Asl; Bebek, Nerses; Tsai, Menghan; Ho, Chenjui; Hsiang Lin, Chih; Lin, Kuanglin; Chou, Ijun; Poduri, Annapurna; R Shiedley, Beth; Shain, Catherine; L Noebels, Jeffrey; Goldman, Alicia; M Busch, Robyn; Jehi, Lara; M Najm, Imad; Ferguson, Lisa; Khoury, Jean; A Glauser, Tracy; O Clark, Peggy; J Buono, Russell; N Ferraro, Thomas; R Sperling, Michael; Lo, Warren; Privitera, Michael; A French, Jac queline; Schachter, Steven; I Kuzniecky, Ruben; Devinsky, Orrin; Hegde, Manu; A Greenberg, David; A Ellis, Colin; Goldberg, Ethan; L Helbig, Katherine; Cosico, Mahgenn; Vaidis waran, Priya; Fitch, Eryn; F Berkovic, Samuel; Lerche, Holger; H Lowenstein, Daniel; B Goldstein, David
Focal Neuromyotonia Associated With a C9ORF72 Expansion Mutation 1-gen-2020 Francesco Fortunato ; Giuseppe Bonapace ; Rosa Gullace ; Monica Gagliardi ; Rita Nisticò ; Paola Valentino ; Antonio Gambardella
Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome 1-gen-2019 Bonapace, Giuseppe; Gullace, Rosa; Concolino, Daniela; Iannello, Grazia; Procopio, Radha; Gagliardi, Monica; Arabia, Gennarina; Barbagallo, Gaetano; Lupo, Angela; Manfredini Lucia, Ilaria; Annesi, Grazia; Quattrone, Aldo
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals 1-gen-2019 Feng, Yca; Howrigan, Dp; Abbott, Le; Tashman, K; Cerrato, F; Singh, T; Heyne, H; Byrnes, A; Churchhouse, C; Watts, N; Solomonson, M; Lal, D; Heinzen, El; Dhindsa, Rs; Stanley, Ke; Cavalleri, Gl; Hakonarson, H; Helbig, I; Krause, R; May, P; Weckhuysen, S; Petrovski, S; Kamalakaran, S; Sisodiya, Sm; Cossette, P; Cotsapas, C; De Jonghe, P; Dixonsalazar, T; Guerrini, R; Kwan, P; Marson, Ag; Stewart, R; Depondt, C; Dlugos, Dj; Scheffer, Ie; Striano, P; Freyer, C; Mckenna, K; Regan, Bm; Bellows, St; Leu, C; Bennett, Ca; Johns, Emc; Macdonald, A; Shilling, H; Burgess, R; Weckhuysen, D; Bahlo, M; O'Brien, Tj; Todaro, M; Stamberger, H; Andrade, Dm; Sadoway, Tr; Mo, K; Krestel, H; Gallati, S; Papacostas, Ss; Kousiappa, I; Tanteles, Ga; Sterbova, K; Vlckova, M; Sedlackova, L; Lassuthova, P; Klein, Km; Rosenow, F; Reif, Ps; Knake, S; Kunz, Ws; Zsurka, G; Elger, Ce; Bauer, J; Rademacher, M; Pendziwiat, M; Muhle, H; Rademacher, A; van Baalen, A; von Spiczak, S; Stephani, U; Afawi, Z; Korczyn, Ad; Kanaan, M; Canavati, C; Kurlemann, G; Mullerschluter, K; Kluger, G; Hausler, M; Blatt, I; Lemke, Jr; Krey, I; Weber, Yg; Wolking, S; Becker, F; Hengsbach, C; Rau, S; Maisch, Af; Steinhoff, Bj; Schulzebonhage, A; Schubertbast, S; Schreiber, H; Borggrafe, I; Schankin, Cj; Mayer, T; Korinthenberg, R; Brockmann, K; Dennig, D; Madeleyn, R; Kalviainen, R; Auvinen, P; Saarela, A; Linnankivi, T; Lehesjoki, Ae; Rees, Mi; Chung, Sk; Pickrell, Wo; Powell, R; Schneider, N; Balestrini, S; Zagaglia, S; Braatz, V; Johnson, Mr; Auce, P; Sills, Gj; Baum, Lw; Sham, Pc; Cherny, Ss; Lui, Cht; Barisic, N; Delanty, N; Doherty, Cp; Shukralla, A; Mccormack, M; Elnaggar, H; Canafoglia, L; Franceschetti, S; Castellotti, B; Granata, T; Zara, F; Iacomino, M; Madia, F; Vari, Ms; Mancardi, Mm; Salpietro, V; Bisulli, F; Tinuper, P; Licchetta, L; Pippucci, T; Stipa, C; Minardi, R; Gambardella, A; Labate, A; Annesi, G; Manna, L; Gagliardi, M; Parrini, E; Mei, D; Vetro, A; Bianchini, C; Montomoli, M; Doccini, V; Marini, C; Suzuki, T; Inoue, Y; Yamakawa, K; Tumiene, B; Sadleir, Lg; King, C; Mountier, E; Caglayan, Sh; Arslan, M; Yapici, Z; Yis, U; Topaloglu, P; Kara, B; Turkdogan, D; Gundogdueken, A; Bebek, N; Uguriseri, S; Baykan, B; Salman, B; Haryanyan, G; Yucesan, E; Kesim, Y; Ozkara, C; Poduri, A; Shiedley, Br; Shain, C; Buono, Rj; Ferraro, Tn; Sperling, Mr; Lo, W; Privitera, M; French, Ja; Schachter, S; Kuzniecky, Ri; Devinsky, O; Hegde, M; Khankhanian, P; Helbig, Kl; Ellis, Ca; Spalletta, G; Piras, F; Piras, F; Gili, T; Ciullo, V; Reif, A; Mcquillin, A; Bass, N; Mcintosh, A; Blackwood, D; Johnstone, M; Palotie, A; Pato, Mt; Pato, Cn; Bromet, Ej; Carvalho, Cb; Achtyes, Ed; Azevedo, Mh; Kotov, R; Lehrer, Ds; Malaspina, D; Marder, Sr; Medeiros, H; Morley, Cp; Perkins, Do; Sobell, Jl; Buckley, Pf; Macciardi, F; Rapaport, Mh; Knowles, Ja; Fanous, Ah; Mccarroll, Sa; Gupta, N; Gabriel, Sb; Daly, Mj; Lander, Es; Lowenstein, Dh; Goldstein, Db; Lerche, H; Berkovic, Sf; Neale, Bm
A new CHCHD2 mutation identified in a southern italy patient with multiple system atrophy 1-gen-2018 Giuseppe Nicooletti ; Monica Gagliardi ; Radha Procopio ; Grazia Iannello ; Maurizio Morelli ; Grazia Annesi ; Aldo Quattrone ;
Neuropsychological heterogeneity in patients with primary familial brain calcification due to a novel mutation in SLC20A2 1-gen-2018 Chiriaco, Carmelina; Novellino, Fabiana; Salsone, Maria; Gagliardi, Monica; Morelli, Maurizio; Quattrone, Aldo
A SLC20A2 mutation identified in an asymptomatic patient with brain calcification 1-gen-2017 Gagliardi, M; Morelli, M; Iannello, G; Colica, C; Annesi, G; Quattrone, A
AKT1(E17K) Is Oncogenic in Mouse Lung and Cooperates with Chemical Carcinogens in Inducing Lung Cancer 1-gen-2016 Malanga, Donatella; Belmonte, Stefania; Colelli, Fabiana; Scarfo, Marzia; De Marco, Carmela; Oliveira, Duarte Mendes; Mirante, Teresa; Camastra, Caterina; Gagliardi, Monica; Rizzuto, Antonia; Mignogna, Chiara; Paciello, Orlando; Papparella, Serenella; Fagman, Henrik; Viglietto, Giuseppe
Analysis of CHCHD2 gene in familial Parkinson’s disease from Calabria 1-gen-2016 Gagliardi, Monica; Iannello, Grazia; Colica, Carmela; Annesi, Grazia; Quattrone, Aldo
FTH1P3, a Novel H-Ferritin Pseudogene Transcriptionally Active, Is Ubiquitously Expressed and Regulated during Cell Differentiation 1-gen-2016 Di Sanzo, Maddalena; Aversa, Ilenia; Santamaria, Gianluca; Gagliardi, Monica; Panebianco, Mariafranca; Biamonte, Flavia; Zolea, Fabiana; Faniello Maria, Concetta; Cuda, Giovanni; Costanzo, Francesco
Mutational analysis of COASY in an Italian patient with NBIA 1-gen-2016 Annesi, G; Gagliardi, M; Iannello, G; Quattrone, A
Voxel-based morphometry to detect effect of APOE on brain gray matter changes in Parkinson's Disease. 1-gen-2016 Nicoletti, Giuseppe; Manners David, Neil; Novellino, Fabiana; Testa, Claudia; Gagliardi, Monica; Tonon, Caterina; Lodi, Raffaele; Quattrone, Aldo
Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP. 1-gen-2013 Labate, A; Tarantino, P; Palamara, G; Gagliardi, M; Cavalcanti, F; Ferlazzo, E; Sturniolo, M; Incorpora, G; Annesi, G; Aguglia, U; Gambardella, A