Bernardo Dalla Bernardina
University of Verona
148 Papers
1.2K Citations
Bernardo Dalla Bernardina is an academic researcher from University of Verona. The author has contributed to research in topics: Epilepsy & Medicine. The author has an hindex of 42, co-authored 134 publications.
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Papers
The Relationship between Body Size and Depression Symptoms in Adolescents
Samuele Cortese,Bruno Falissard,Marco Angriman,Yolande Pigaiani,Claudia Banzato,Giovanna Bogoni,Maristella Pellegrino,Solange Cook,Franco Pajno-Ferrara,Bernardo Dalla Bernardina,Marie Christine Mouren,Claudio Maffeis +11 more
TL;DR: The relationship between body size and depressive symptoms in young adolescents is curvilinear and is moderated by sex.
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Concordance of clinical forms of epilepsy in families with several affected members
Amedeo Bianchi,Giuliano Avanzini,Bernardo Dalla Bernardina,Raffaele Canger,Carlo Alberto Tassinari,Federico Vigevano,A. Tiezzi,G. Buzzi,C. Fani,C. Devermandois,P. Zolo,A. Antonelli,Simona Binelli,Daniela Buti,Maria Paola Canevini,A. Carullo,C. Ciarmatori,Giangennaro Coppola,Patrizia D'Alessandro,M. Defeo,S. Didonato,C. Durisotti,C. Roso,A. Francia,Carlo Andrea Galimberti,R Galli,P. Garofalo,Paola Rossi,C. Iani,Roberto Mai,Mario Manfredi,N. Margiotta,Roberto Massetani,Salvatore Mazza,Oriano Mecarelli,Antonia Parmeggiani,A. Pascotto,Stefano Ricci,Raffaele Rocchi,G. Romano,A. Saltareli,M. Santucci,G. Sideri,Luigi Maria Specchio,Amelia Tartara,Camillo Tiacci,Giampaolo Vatti,Piernanda Vigliano,Lilia Volpi +48 more
TL;DR: A rare association between childhood absence epilepsy (CAE) and juvenile myoclonic epilepsy (JME) is observed, and in every idiopathic form of epilepsy, there was a high concordance for the seizure phenotype in first‐degree affected relatives, whereas in more distantly related family members concordances was less evident and there were a tendency toward a different phenotypic expression.
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Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk
F. Kyle Satterstrom,F. Kyle Satterstrom,Jack A. Kosmicki,Jiebiao Wang,Michael S. Breen,Silvia De Rubeis,Joon Yong An,Minshi Peng,Ryan Collins,Jakob Grove,Jakob Grove,Lambertus Klei,Christine Stevens,Jennifer Reichert,Maureen Mulhern,Mykyta Artomov,Sherif Gerges,Brooke Sheppard,Xinyi Xu,Aparna Bhaduri,Utku Norman,Harrison Brand,Grace Schwartz,Rachel Nguyen,Elizabeth E. Guerrero,Caroline Dias,Branko Aleksic,Richard Anney,Mafalda Barbosa,Somer L. Bishop,Alfredo Brusco,Jonas Bybjerg-Grauholm,Jonas Bybjerg-Grauholm,Angel Carracedo,Marcus C.Y. Chan,Andreas G. Chiocchetti,Brian H.Y. Chung,Hilary Coon,Michael L. Cuccaro,Aurora Currò,Bernardo Dalla Bernardina,Ryan N. Doan,Enrico Domenici,Shan Dong,Chiara Fallerini,Montserrat Fernández-Prieto,Giovanni Battista Ferrero,Christine M. Freitag,Menachem Fromer,J. Jay Gargus,Daniel H. Geschwind,Elisa Giorgio,Javier González-Peñas,Stephen J. Guter,Danielle Halpern,Emily Hansen-Kiss,Xin He,Gail E. Herman,Irva Hertz-Picciotto,David M. Hougaard,David M. Hougaard,Christina M. Hultman,Iuliana Ionita-Laza,Suma Jacob,Jesslyn Jamison,Astanand Jugessur,Miia Kaartinen,Gun Peggy Knudsen,Alexander Kolevzon,Itaru Kushima,So Lun Lee,Terho Lehtimäki,Elaine T. Lim,Carla Lintas,W. Ian Lipkin,Diego Lopergolo,Fátima Lopes,Yunin Ludena,Patrícia Maciel,Per Magnus,Behrang Mahjani,Nell Maltman,Dara S. Manoach,Gal Meiri,Idan Menashe,Judith Miller,Nancy J. Minshew,Eduarda Montenegro M. de Souza,Danielle de Paula Moreira,Eric M. Morrow,Ole Mors,Ole Mors,Preben Bo Mortensen,Matthew W. Mosconi,Pierandrea Muglia,Benjamin M. Neale,Benjamin M. Neale,Merete Nordentoft,Merete Nordentoft,Norio Ozaki,Aarno Palotie,Mara Parellada,Maria Rita Passos-Bueno,Margaret A. Pericak-Vance,Antonio M. Persico,Isaac N. Pessah,Kaija Puura,Abraham Reichenberg,Alessandra Renieri,Evelise Riberi,Elise B. Robinson,Elise B. Robinson,Kaitlin E. Samocha,Sven Sandin,Sven Sandin,Susan L. Santangelo,Susan L. Santangelo,Gerry Schellenberg,Stephen W. Scherer,Stephen W. Scherer,Sabine Schlitt,Rebecca J. Schmidt,Lauren M. Schmitt,Isabela Maya Wahys Silva,Tarjinder Singh,Tarjinder Singh,Paige M. Siper,Moyra Smith,Gabriela Soares,Camilla Stoltenberg,Pål Surén,Ezra Susser,Ezra Susser,John A. Sweeney,Peter Szatmari,Lara Tang,Flora Tassone,Karoline Teufel,Elisabetta Trabetti,Maria del Pilar Trelles,Christopher A. Walsh,Lauren A. Weiss,Thomas Werge,Thomas Werge,Donna M. Werling,Emilie M. Wigdor,Emilie M. Wigdor,Emma Wilkinson,A. Jeremy Willsey,Timothy W. Yu,Mullin H.C. Yu,Ryan Yuen,Elaine Cristina Zachi,Catalina Betancur,Edwin H. Cook,Louise Gallagher,Michael Gill,Thomas Lehner,Geetha Senthil,James S. Sutcliffe,Audrey Thurm,Michael E. Zwick,Anders D. Børglum,Matthew W. State,A. Ercument Cicek,A. Ercument Cicek,Michael E. Talkowski,David J. Cutler,Bernie Devlin,Stephen Sanders,Kathryn Roeder,Joseph D. Buxbaum,Mark J. Daly +172 more
TL;DR: The largest exome sequencing study to date focused on rare variation in autism spectrum disorder (ASD) is presented, and 99 genes in ASD risk are implicate at a false discovery rate of 0.1, implying that disruption of these genes alters the development of both neuron types.
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4p^- Syndrome: A Chromosomal Disorder Associated with a Particular EEG Pattern
V. Sgro,Enrica Riva,Maria Paola Canevini,V. Colamaria,A. Rottoli,Lorella Minotti,Raffaele Canger,Bernardo Dalla Bernardina +7 more
TL;DR: It is suggested that the electroclinical picture common to WHS and AS might represent a characteristic type of epilepsy linked to a common genetic abnormality.
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EEG of a Nocturnal Seizure in a Patient with “Benign Epilepsy of Childhood with Rolandic Spikes”
TL;DR: The fust EEG recording is reported of a child with “benign epilepsy of childhood with Rolandic spikes” during a partial motor (facial) seizure, which occurred during Phase II of natural sleep.
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