Resultados da busca - Maurizio Elia

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  1. 1
    Considerations in Translating AI to Improve Care

    Considerations in Translating AI to Improve Care por Divneet Mandair, Maurizio Elia, Julian C. Hong

    Publicado em 2025
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  2. 2
    Executive Functions and Adaptive Behaviour in Autism Spectrum Disorders with and without Intellectual Disability

    Executive Functions and Adaptive Behaviour in Autism Spectrum Disorders with and without Intellectual Disability por Simonetta Panerai, Domenica Tasca, Raffaele Ferri, Valentina Genitori D’Arrigo, Maurizio Elia

    Publicado em 2014
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  3. 3
    Cyclic alternating pattern and spectral analysis of heart rate variability during normal sleep

    Cyclic alternating pattern and spectral analysis of heart rate variability during normal sleep por Raffaele Ferri, Liborio Parrino, Arianna Smerieri, M. G. Terzano, Maurizio Elia, S Musumeci, Salvatore Pettinato

    Publicado em 2000
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  4. 4
    Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome

    Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome por S Musumeci, Paolo Bosco, Giuseppe Calabrese, Cathy Bakker, Giovanni Battista De Sarro, Maurizio Elia, Raffaele Ferri, Ben A. Oostra

    Publicado em 2000
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  5. 5
    Whole Exome Sequencing as a First-Line Molecular Genetic Test in Developmental and Epileptic Encephalopathies

    Whole Exome Sequencing as a First-Line Molecular Genetic Test in Developmental and Epileptic Encephalopathies por Luigi Vetri, Francesco Calı̀, Salvatore Saccone, Mirella Vinci, Valeria Chiavetta, Marco Carotenuto, Michele Roccella, Carola Costanza, Maurizio Elia

    Publicado em 2024
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  6. 6
    Epilepsy and EEG Findings in Males with Fragile X Syndrome

    Epilepsy and EEG Findings in Males with Fragile X Syndrome por S Musumeci, Randi J. Hagerman, Raffaele Ferri, Paolo Bosco, Bernardo Dalla Bernardina, C. A. Tassinari, Giovambattista De Sarro, Maurizio Elia

    Publicado em 1999
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  7. 7
    A de novo ARIH2 gene mutation was detected in a patient with autism spectrum disorders and intellectual disability

    A de novo ARIH2 gene mutation was detected in a patient with autism spectrum disorders and intellectual disability por Mirella Vinci, Simone Treccarichi, Rosanna Galati Rando, Antonino Musumeci, Valeria Todaro, Concetta Federico, Salvatore Saccone, Maurizio Elia, Francesco Calı̀

    Publicado em 2024
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  8. 8
    A novel <i>KCNQ3</i> mutation in familial epilepsy with focal seizures and intellectual disability

    A novel <i>KCNQ3</i> mutation in familial epilepsy with focal seizures and intellectual disability por Francesco Miceli, Pasquale Striano, Maria Virginia Soldovieri, Antonina Fontana, Rosaria Nardello, Angela Robbiano, Giulia Bellini, Maurizio Elia, Federico Zara, Maurizio Taglialatela, Salvatore Mangano

    Publicado em 2014
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  9. 9
    The pharmacological management of Lennox-Gastaut syndrome and critical literature review

    The pharmacological management of Lennox-Gastaut syndrome and critical literature review por Alberto Verrotti, Pasquale Striano, Giulia Iapadre, Luca Zagaroli, Paolo Bonanni, Giangennaro Coppola, Maurizio Elia, Oriano Mecarelli, Emilio Franzoni, Paola De Liso, Federico Vigevano, Paolo Curatolo

    Publicado em 2018
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  10. 10
    miRNAs Plasma Profiles in Vascular Dementia: Biomolecular Data and Biomedical Implications

    miRNAs Plasma Profiles in Vascular Dementia: Biomolecular Data and Biomedical Implications por Marco Ragusa, Paolo Bosco, Lucia Tamburello, Cristina Barbagallo, Angelo Giuseppe Condorelli, Mariangela Tornitore, Rosario S. Spada, Davide Barbagallo, Marina Scalia, Maurizio Elia, Cinzia Di Pietro, Michele Purrello

    Publicado em 2016
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  11. 11
    A genetic variant that disrupts <i>MET</i> transcription is associated with autism

    A genetic variant that disrupts <i>MET</i> transcription is associated with autism por Jerry L. Campbell, James S. Sutcliffe, Philip J. Ebert, Roberto Militerni, Carmela Bravaccio, Simona Trillo, Maurizio Elia, Cindy Schneider, Raun D. Melmed, Roberto Sacco, Antonio M. Persico, Pat Levitt

    Publicado em 2006
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  12. 12
    Principal pathogenetic components and biological endophenotypes in autism spectrum disorders

    Principal pathogenetic components and biological endophenotypes in autism spectrum disorders por Roberto Sacco, Paolo Curatolo, Barbara Manzi, Roberto Militerni, Carmela Bravaccio, Alessandro Frolli, C Lenti, Monica Saccani, Maurizio Elia, Karl‐Ludvig Reichelt, Tiziana Pascucci, Stefano Puglisi‐Allegra, Antonio M. Persico

    Publicado em 2010
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  13. 13
    Methodology of photic stimulation revisited: Updated European algorithm for visual stimulation in the EEG laboratory

    Methodology of photic stimulation revisited: Updated European algorithm for visual stimulation in the EEG laboratory por Dorothee Kasteleijn‐Nolst Trenité, Guido Rubboli, Édouard Hirsch, António Martins da Silva, Stefano Seri, Arnold J. Wilkins, Jaime Parra, Athanasios Covanis, Maurizio Elia, Giuseppe Capovilla, Ulrich Stephani, G. F. A. Harding

    Publicado em 2011
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  14. 14
    Summary of recommendations for the management of infantile seizures: Task<scp>F</scp>orce<scp>R</scp>eport for the<scp>ILAE C</scp>ommission of<scp>P</scp>ediatrics

    Summary of recommendations for the management of infantile seizures: Task<scp>F</scp>orce<scp>R</scp>eport for the<scp>ILAE C</scp>ommission of<scp>P</scp>ediatrics por Jo M. Wilmshurst, William D. Gaillard, Kollencheri Puthenveettil Vinayan, Tammy N. Tsuchida, Perrine Plouin, Patrick Van Bogaert, Jaime Carrizosa, Maurizio Elia, Dana Craiu, N. Jović, Doug Nordli, Deborah Hirtz, Virginia Wong, Tracy A. Glauser, Eli M. Mizrahi, J. Helen Cross

    Publicado em 2015
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  15. 15
    Lacosamide in pediatric and adult patients: Comparison of efficacy and safety

    Lacosamide in pediatric and adult patients: Comparison of efficacy and safety por Alberto Verrotti, Giulia Loiacono, Antonella Pizzolorusso, Pasquale Parisi, Oliviero Bruni, Anna Luchetti, Nelia Zamponi, Silvia Cappanera, Salvatore Grosso, Gerhard Kluger, Christine Janello, Emilio Franzoni, Maurizio Elia, Alberto Spalice, Giangennaro Coppola, Pasquale Striano, Piero Pavone, Salvatore Savasta, Maurizio Viri, Antonino Romeo, Paolo Aloisi, Giuseppe Gobbi, Alessandro Ferretti, Raffaella Cusmai, Paolo Curatolo

    Publicado em 2013
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  16. 16
    A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy

    A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy por Ida Manna, Antonio Gambardella, Amedeo Bianchi, Pasquale Striano, Rossana Tozzi, Umberto Aguglia, Francesca Beccaria, Paolo Benna, R. Campostrini, Maria Paola Canevini, Francesca Condino, C. Durisotti, Maurizio Elia, Anna Teresa Giallonardo, Alfonso Iudice, Angelo Labate, Angela La Neve, Roberto Michelucci, Gian Carlo Muscas, Roberta Paravidino, Gaetano Zaccara, Claudio Zucca, Federico Zara, Emilio Perucca

    Publicado em 2011
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  17. 17
    Adjunctive cenobamate in people with focal onset seizures: Insights from the Italian Expanded Access Program

    Adjunctive cenobamate in people with focal onset seizures: Insights from the Italian Expanded Access Program por Roberta Roberti, Giovanni Assenza, Francesca Bisulli, Giovanni Boero, Laura Canafoglia, Valentina Chiesa, Carlo Di Bonaventura, Giancarlo Di Gennaro, Maurizio Elia, Edoardo Ferlazzo, Alfonso Giordano, Angela La Neve, Claudio Liguori, Stefano Meletti, Francesca Felicia Operto, Nicola Pietrafusa, Monica Puligheddu, Patrizia Pulitano, Eleonora Rosati, Ilaria Sammarra, Elena Tartara, Giampaolo Vatti, Flavio Villani, Emilio Russo, Simona Lattanzi

    Publicado em 2024
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  18. 18
    <i>SCN1A</i> duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

    <i>SCN1A</i> duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis por Carla Marini, Ingrid E. Scheffer, Rima Nabbout, Davide Mei, Kathy Cox, Leanne M. Dibbens, Jacinta M. McMahon, Xenia Iona, Rochio Sanchez Carpintero, Maurizio Elia, Maria Roberta Cilio, Nicola Specchio, Lucio Giordano, Pasquale Striano, Elena Di Gennaro, J. Helen Cross, Sara Kivity, Miriam Y. Neufeld, Zaid Afawi, Eva Andermann, Daniel Keene, Olivier Dulac, Federico Zara, Samuel F. Berkovic, Renzo Guerrini, John C. Mulley

    Publicado em 2009
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  19. 19
    Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype–Phenotype Correlations

    Brain MRI Findings in Severe Myoclonic Epilepsy in Infancy and Genotype–Phenotype Correlations por Pasquale Striano, Maria Margherita Mancardi, Roberta Biancheri, Francesca Madia, Elena Di Gennaro, Roberta Paravidino, Francesca Beccaria, Giuseppe Capovilla, Bernardo Dalla Bernardina, Francesca Darra, Maurizio Elia, Lucio Giordano, Giuseppe Gobbi, Tiziana Granata, Francesca Ragona, Renzo Guerrini, Carla Marini, Davide Mei, Francesca Longaretti, Antonino Romeo, Laura Siri, Nicola Specchio, Federico Vigevano, Salvatore Striano, Fabio Tortora, Andrea Rossi, Carlo Minetti, Charlotte Dravet, R. Gaggero, Federico Zara

    Publicado em 2007
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  20. 20
    Treatment of seizures in the neonate: Guidelines and consensus‐based recommendations—Special report from the <scp>ILAE</scp> Task Force on Neonatal Seizures

    Treatment of seizures in the neonate: Guidelines and consensus‐based recommendations—Special report from the <scp>ILAE</scp> Task Force on Neonatal Seizures por Ronit Pressler, Nicholas S. Abend, Stéphane Auvin, Geraldine B. Boylan, Francesco Brigo, Maria Roberta Cilio, Linda S. de Vries, Maurizio Elia, Alberto Espeche, Cecil D. Hahn, Terrie E. Inder, Nathalie Jetté, Angelina Kakooza‐Mwesige, Silke Mader, Eli M. Mizrahi, Solomon L. Moshé, Lakshmi Nagarajan, Iris Noyman, Magda Lahorgue Nunes, Pauline Samia, Eilon Shany, Renée A. Shellhaas, Ann Subota, Chahnez Triki, Tammy N. Tsuchida, Kollencheri Puthenveettil Vinayan, Jo M. Wilmshurst, Elissa Yozawitz, Hans Hartmann

    Publicado em 2023
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