Works matching AU Striano, Pasquale

Results: 367
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    Electroencephalography in Autism Spectrum Disorder.

    Published in:
    Journal of Clinical Medicine, 2025, v. 14, n. 6, p. 1882, doi. 10.3390/jcm14061882
    By:
    • Hankus, Magdalena;
    • Ochman-Pasierbek, Patrycja;
    • Brzozowska, Malwina;
    • Striano, Pasquale;
    • Paprocka, Justyna
    Publication type:
    Article
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    Temporal Lobe Epilepsy and Psychiatric Comorbidity.

    Published in:
    Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.775781
    By:
    • Vinti, Valerio;
    • Dell'Isola, Giovanni Battista;
    • Tascini, Giorgia;
    • Mencaroni, Elisabetta;
    • Cara, Giuseppe Di;
    • Striano, Pasquale;
    • Verrotti, Alberto
    Publication type:
    Article
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    Functional Gastrointestinal Disorders in Patients With Epilepsy: Reciprocal Influence and Impact on Seizure Occurrence.

    Published in:
    Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.705126
    By:
    • Avorio, Federica;
    • Cerulli Irelli, Emanuele;
    • Morano, Alessandra;
    • Fanella, Martina;
    • Orlando, Biagio;
    • Albini, Mariarita;
    • Basili, Luca M.;
    • Ruffolo, Gabriele;
    • Fattouch, Jinane;
    • Manfredi, Mario;
    • Russo, Emilio;
    • Striano, Pasquale;
    • Carabotti, Marilia;
    • Giallonardo, Anna T.;
    • Severi, Carola;
    • Di Bonaventura, Carlo
    Publication type:
    Article
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    Neuromuscular and Neuroendocrinological Features Associated With ZC4H2 -Related Arthrogryposis Multiplex Congenita in a Sicilian Family: A Case Report.

    Published in:
    Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.704747
    By:
    • Piccolo, Gianluca;
    • d'Annunzio, Giuseppe;
    • Amadori, Elisabetta;
    • Riva, Antonella;
    • Borgia, Paola;
    • Tortora, Domenico;
    • Maghnie, Mohamad;
    • Minetti, Carlo;
    • Gitto, Eloisa;
    • Iacomino, Michele;
    • Baldassari, Simona;
    • Fiorillo, Chiara;
    • Zara, Federico;
    • Striano, Pasquale;
    • Salpietro, Vincenzo
    Publication type:
    Article
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    ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy.

    Published in:
    Epilepsy Research & Treatment, 2011, p. 1, doi. 10.1155/2011/258365
    By:
    • Rigon, Laura;
    • Vettori, Andrea;
    • Busolin, Giorgia;
    • Egeo, Gabriella;
    • Pulitano, Patrizia;
    • Santulli, Lia;
    • Pasini, Elena;
    • Striano, Pasquale;
    • la Neve, Angela;
    • Dri, Valeria Vianello;
    • Boniver, Clementina;
    • Gambardella, Antonio;
    • Banfi, Paola;
    • Binelli, Simona;
    • Di Bonaventura, Carlo;
    • Striano, Salvatore;
    • de Falco, Fabrizio;
    • Giallonardo, Anna T.;
    • Mecarelli, Oriano;
    • Michelucci, Roberto
    Publication type:
    Article
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    Ictal video‐electroencephalogram of breath‐holding attack.

    Published in:
    Journal of Paediatrics & Child Health, 2023, v. 59, n. 10, p. 1171, doi. 10.1111/jpc.16480
    By:
    • Dilena, Robertino;
    • Biffi, Giulia;
    • Mauri, Eleonora;
    • Lelii, Mara;
    • Zazzeron, Laura;
    • Bana, Cristina;
    • Barbieri, Sergio;
    • Marchisio, Paola;
    • Striano, Pasquale;
    • Cappellari, Alberto
    Publication type:
    Article
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    Novel causative variants in Legius syndrome: SPRED1 Genotype spectrum expansion.

    Published in:
    American Journal of Medical Genetics. Part A, 2024, v. 194, n. 12, p. 1, doi. 10.1002/ajmg.a.63824
    By:
    • Chelleri, Cristina;
    • Brolatti, Noemi;
    • De Marco, Patrizia;
    • Ognibene, Marzia;
    • Diana, Maria Cristina;
    • Madia, Francesca;
    • Duca, Marco Di;
    • Santangelo, Andrea;
    • Capra, Valeria;
    • Striano, Pasquale;
    • Zara, Federico;
    • Scala, Marcello
    Publication type:
    Article
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    Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical Development.

    Published in:
    Frontiers in Neuroscience, 2020, v. 14, p. 1, doi. 10.3389/fnins.2020.00644
    By:
    • Iacomino, Michele;
    • Baldassari, Simona;
    • Tochigi, Yuki;
    • Kośla, Katarzyna;
    • Buffelli, Francesca;
    • Torella, Annalaura;
    • Severino, Mariasavina;
    • Paladini, Dario;
    • Mandarà, Luana;
    • Riva, Antonella;
    • Scala, Marcello;
    • Balagura, Ganna;
    • Accogli, Andrea;
    • Nigro, Vincenzo;
    • Minetti, Carlo;
    • Fulcheri, Ezio;
    • Zara, Federico;
    • Bednarek, Andrzej K.;
    • Striano, Pasquale;
    • Suzuki, Hiroetsu
    Publication type:
    Article
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    Fenfluramine treatment for Dravet syndrome: Long term real‐world analysis demonstrates safety and reduced health care burden.

    Published in:
    Epilepsia (Series 4), 2025, v. 66, n. 4, p. 1110, doi. 10.1111/epi.18241
    By:
    • Boncristiano, Alessandra;
    • Balestrini, Simona;
    • Doccini, Viola;
    • Specchio, Nicola;
    • Pietrafusa, Nicola;
    • Trivisano, Marina;
    • Darra, Francesca;
    • Cossu, Alberto;
    • Battaglia, Domenica;
    • Quintiliani, Michela;
    • Gambardella, M. Luigia;
    • Parente, Eliana;
    • Monni, Rita;
    • Matricardi, Sara;
    • Marini, Carla;
    • Ragona, Francesca;
    • Granata, Tiziana;
    • Striano, Pasquale;
    • Riva, Antonella;
    • Guerrini, Renzo
    Publication type:
    Article
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    Long‐term effectiveness of add‐on perampanel in patients with Lennox–Gastaut syndrome: A multicenter retrospective study.

    Published in:
    Epilepsia (Series 4), 2023, v. 64, n. 6, p. e98, doi. 10.1111/epi.17601
    By:
    • Matricardi, Sara;
    • Cesaroni, Elisabetta;
    • Bonanni, Paolo;
    • Foschi, Nicoletta;
    • D′Aniello, Alfredo;
    • Di Gennaro, Giancarlo;
    • Striano, Pasquale;
    • Cappanera, Silvia;
    • Siliquini, Sabrina;
    • Freri, Elena;
    • Ragona, Francesca;
    • Granata, Tiziana;
    • Deleo, Francesco;
    • Villani, Flavio;
    • Russo, Angelo;
    • Messana, Tullio;
    • Siri, Laura;
    • Bagnasco, Irene;
    • Vignoli, Aglaia;
    • Operto, Francesca Felicia
    Publication type:
    Article
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    De novo KCNA6 variants with attenuated K<sub>V</sub>1.6 channel deactivation in patients with epilepsy.

    Published in:
    Epilepsia (Series 4), 2023, v. 64, n. 2, p. 443, doi. 10.1111/epi.17455
    By:
    • Salpietro, Vincenzo;
    • Galassi Deforie, Valentina;
    • Efthymiou, Stephanie;
    • O'Connor, Emer;
    • Marcé‐Grau, Anna;
    • Maroofian, Reza;
    • Striano, Pasquale;
    • Zara, Federico;
    • Morrow, Michelle M.;
    • Reich, Adi;
    • Blevins, Amy;
    • Sala‐Coromina, Júlia;
    • Accogli, Andrea;
    • Fortuna, Sara;
    • Alesandrini, Marie;
    • Au, P. Y. Billie;
    • Singhal, Nilika Shah;
    • Cogne, Benjamin;
    • Isidor, Bertrand;
    • Hanna, Michael G.
    Publication type:
    Article
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    A randomized, double‐blind trial of triheptanoin for drug‐resistant epilepsy in glucose transporter 1 deficiency syndrome.

    Published in:
    Epilepsia (Series 4), 2022, v. 63, n. 7, p. 1748, doi. 10.1111/epi.17263
    By:
    • Striano, Pasquale;
    • Auvin, Stéphane;
    • Collins, Abigail;
    • Horvath, Rita;
    • Scheffer, Ingrid E.;
    • Tzadok, Michal;
    • Miller, Ian;
    • Kay Koenig, Mary;
    • Lacy, Adrian;
    • Davis, Ronald;
    • Garcia‐Cazorla, Angela;
    • Saneto, Russell P.;
    • Brandabur, Melanie;
    • Blair, Susan;
    • Koutsoukos, Tony;
    • De Vivo, Darryl
    Publication type:
    Article
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    A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam.

    Published in:
    Epilepsia (Series 4), 2022, v. 63, n. 6, p. 1563, doi. 10.1111/epi.17228
    By:
    • Campbell, Ciarán;
    • McCormack, Mark;
    • Patel, Sonn;
    • Stapleton, Caragh;
    • Bobbili, Dheeraj;
    • Krause, Roland;
    • Depondt, Chantal;
    • Sills, Graeme J.;
    • Koeleman, Bobby P.;
    • Striano, Pasquale;
    • Zara, Federico;
    • Sander, Josemir W.;
    • Lerche, Holger;
    • Kunz, Wolfram S.;
    • Stefansson, Kari;
    • Stefansson, Hreinn;
    • Doherty, Colin P.;
    • Heinzen, Erin L.;
    • Scheffer, Ingrid E.;
    • Goldstein, David B.
    Publication type:
    Article
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    Expanding the phenotype of PIGS‐associated early onset epileptic developmental encephalopathy.

    Published in:
    Epilepsia (Series 4), 2021, v. 62, n. 2, p. e35, doi. 10.1111/epi.16801
    By:
    • Efthymiou, Stephanie;
    • Dutra‐Clarke, Marina;
    • Maroofian, Reza;
    • Kaiyrzhanov, Rauan;
    • Scala, Marcello;
    • Reza Alvi, Javeria;
    • Sultan, Tipu;
    • Christoforou, Marilena;
    • Tuyet Mai Nguyen, Thi;
    • Mankad, Kshitij;
    • Vona, Barbara;
    • Rad, Aboulfazl;
    • Striano, Pasquale;
    • Salpietro, Vincenzo;
    • Guillen Sacoto, Maria J.;
    • Zaki, Maha S.;
    • Gleeson, Joseph G.;
    • Campeau, Philippe M.;
    • Russell, Bianca E.;
    • Houlden, Henry
    Publication type:
    Article
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    No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy.

    Published in:
    Epilepsia (Series 4), 2019, v. 60, n. 5, p. e31, doi. 10.1111/epi.14657
    By:
    • Schulz, Herbert;
    • Ruppert, Ann‐Kathrin;
    • Zara, Federico;
    • Madia, Francesca;
    • Iacomino, Michele;
    • S. Vari, Maria;
    • Balagura, Ganna;
    • Minetti, Carlo;
    • Striano, Pasquale;
    • Bianchi, Amedeo;
    • Marini, Carla;
    • Guerrini, Renzo;
    • Weber, Yvonne G.;
    • Becker, Felicitas;
    • Lerche, Holger;
    • Kapser, Claudia;
    • Schankin, Christoph J.;
    • Kunz, Wolfram S.;
    • Møller, Rikke S.;
    • Oliver, Karen L.
    Publication type:
    Article
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    Alterations in the α<sub>2</sub>δ ligand, thrombospondin-1, in a rat model of spontaneous absence epilepsy and in patients with idiopathic/genetic generalized epilepsies.

    Published in:
    Epilepsia (Series 4), 2017, v. 58, n. 11, p. 1993, doi. 10.1111/epi.13898
    By:
    • Santolini, Ines;
    • Celli, Roberta;
    • Cannella, Milena;
    • Imbriglio, Tiziana;
    • Guiducci, Michela;
    • Parisi, Pasquale;
    • Schubert, Julian;
    • Iacomino, Michele;
    • Zara, Federico;
    • Lerche, Holger;
    • Moyanova, Slavianka;
    • Ngomba, Richard Teke;
    • Luijtelaar, Gilles;
    • Battaglia, Giuseppe;
    • Bruno, Valeria;
    • Striano, Pasquale;
    • Nicoletti, Ferdinando;
    • Palotie, Aarno;
    • Folkhälsan, Anna ‐ Elina Lehesjoki;
    • Ruppert, Ann ‐ Kathrin
    Publication type:
    Article
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    Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta-analysis of risk factors.

    Published in:
    Epilepsia (Series 4), 2016, v. 57, n. 8, p. 1205, doi. 10.1111/epi.13448
    By:
    • Ferlazzo, Edoardo;
    • Gasparini, Sara;
    • Beghi, Ettore;
    • Sueri, Chiara;
    • Russo, Emilio;
    • Leo, Antonio;
    • Labate, Angelo;
    • Gambardella, Antonio;
    • Belcastro, Vincenzo;
    • Striano, Pasquale;
    • Paciaroni, Maurizio;
    • Pisani, Laura Rosa;
    • Aguglia, Umberto;
    • Aloisi, Paolo;
    • Arcudi, Luciano;
    • Benna, Paolo;
    • Bianchi, Amedeo;
    • Bogliun, Graziella;
    • Buttinelli, Carla;
    • Campostrini, Roberto
    Publication type:
    Article
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    The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome.

    Published in:
    Epilepsia (Series 4), 2015, v. 56, n. 12, p. e203, doi. 10.1111/epi.13222
    By:
    • Larsen, Jan;
    • Johannesen, Katrine Marie;
    • Ek, Jakob;
    • Tang, Shan;
    • Marini, Carla;
    • Blichfeldt, Susanne;
    • Kibæk, Maria;
    • Spiczak, Sarah;
    • Weckhuysen, Sarah;
    • Frangu, Mimoza;
    • Neubauer, Bernd Axel;
    • Uldall, Peter;
    • Striano, Pasquale;
    • Zara, Federico;
    • Kleiss, Rebecca;
    • Simpson, Michael;
    • Muhle, Hiltrud;
    • Nikanorova, Marina;
    • Jepsen, Birgit;
    • Tommerup, Niels
    Publication type:
    Article
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    Mutations in KCNT1 cause a spectrum of focal epilepsies.

    Published in:
    Epilepsia (Series 4), 2015, v. 56, n. 9, p. e114, doi. 10.1111/epi.13071
    By:
    • Møller, Rikke S.;
    • Heron, Sarah E.;
    • Larsen, Line H. G.;
    • Lim, Chiao Xin;
    • Ricos, Michael G.;
    • Bayly, Marta A.;
    • Kempen, Marjan J. A.;
    • Klinkenberg, Sylvia;
    • Andrews, Ian;
    • Kelley, Kent;
    • Ronen, Gabriel M.;
    • Callen, David;
    • McMahon, Jacinta M.;
    • Yendle, Simone C.;
    • Carvill, Gemma L.;
    • Mefford, Heather C.;
    • Nabbout, Rima;
    • Poduri, Annapurna;
    • Striano, Pasquale;
    • Baglietto, Maria G.
    Publication type:
    Article
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    No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.

    Published in:
    Epilepsia (Series 4), 2015, v. 56, n. 4, p. e40, doi. 10.1111/epi.12944
    By:
    • Mumoli, Laura;
    • Tarantino, Patrizia;
    • Michelucci, Roberto;
    • Bianchi, Amedeo;
    • Labate, Angelo;
    • Franceschetti, Silvana;
    • Marini, Carla;
    • Striano, Pasquale;
    • Gagliardi, Monica;
    • Ferlazzo, Edoardo;
    • Sofia, Vito;
    • Pennese, Loredana;
    • Annesi, Grazia;
    • Aguglia, Umberto;
    • Guerrini, Renzo;
    • Zara, Federico;
    • Gambardella, Antonio
    Publication type:
    Article
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