Resultados da busca - Stella Vari

Todd Paralysis in Rolandic Epilepsy por Pasquale Striano, Maria Stella Vari

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Studying Familial Bainbridge–Ropers Syndrome Due to a Novel <i>ASXL3</i> Germline Variant and Expanding the Clinical Spectrum por Daiana Mariano, Valentina Petrone, Francesca Madia, Mariasavina Severino, Luca Basso, Valeria Capra, Maria Stella Vari, Antonio Marras, Giacomo Tantari, Giuseppe d’Annunzio

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Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus por Antonella Riva, Elisabetta Amadori, Maria Stella Vari, Alberto Spalice, Vincenzo Belcastro, Maurizio Viri, Donatella Capodiferro, Antonino Romeo, Alberto Verrotti, the Delphi panel experts’ group, Pasquale Striano

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Long‐term plasma monitoring of THC and CBD in pediatric drug‐resistant epilepsy: Implications for cannabidiol therapy with Epidyolex® por Alessia Cafaro, Antonella Riva, Federica Pigliasco, Sebastiano Barco, Valentina Manca, Maria Stella Vari, Maria Margherita Mancardi, Lino Nobili, Simona Pichini, Francesco Paolo Busardò, Pasquale Striano, Giuliana Cangemi

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Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet. por Gerarda Cappuccio, Michele Pinelli, Marianna Alagia, Taraka Donti, Debra-Lynn Day-Salvatore, Pierangelo Veggiotti, Valentina De Giorgis, Simona Lunghi, Maria Stella Vari, Pasquale Striano, Nicola Brunetti-Pierri, Adam D Kennedy, Sarah H Elsea

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New Trends and Most Promising Therapeutic Strategies for Epilepsy Treatment por Antonella Riva, Antonella Riva, Alice Golda, Ganna Balagura, Elisabetta Amadori, Elisabetta Amadori, Maria Stella Vari, Gianluca Piccolo, Michele Iacomino, Simona Lattanzi, Vincenzo Salpietro, Vincenzo Salpietro, Carlo Minetti, Carlo Minetti, Pasquale Striano, Pasquale Striano

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Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in <i>KCNA1</i> Impairing the Voltage Sensitivity of Kv1.1 Channel por Paola Imbrici, Andrea Accogli, Rikard Blunck, Concetta Altamura, Michele Iacomino, Maria Cristina D’Adamo, Anna Allegri, Marina Pedemonte, Noemi Brolatti, Stella Vari, Matteo Cataldi, Valeria Capra, Stefano Gustincich, Federico Zara, Jean-Francois Desaphy, Chiara Fiorillo

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Is cognitive profiling in NF1 still optional? A systematic review of current assessment practices por Andrea Santangelo, Andrea Santangelo, Alessandra Sardi, Luca Bergonzini, Luca Bergonzini, Luca Bergonzini, Ilaria Luongo, Federica Mela, Salvatore De Pasquale, Ilaria Cecconi, Maria Stella Vari, Duccio Maria Cordelli, Duccio Maria Cordelli, Maria Cristina Diana, Pasquale Striano, Pasquale Striano

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A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy por Antonella Riva, Roberta Roberti, Gianluca D'Onofrio, Maria Stella Vari, Elisabetta Amadori, Valentina De Giorgis, Caterina Cerminara, Nicola Specchio, Nicola Pietrafusa, Mario Tombini, Giovanni Assenza, Silvia Cappanera, Carla Marini, Paolo Rasmini, Pierangelo Veggiotti, Federico Zara, Emilio Russo, Pasquale Striano

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Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’ project por Elisabetta Amadori, Marcello Scala, Giulia Sofia Cereda, Maria Stella Vari, Francesca Marchese, Veronica Di Pisa, Maria Margherita Mancardi, Thea Giacomini, Laura Siri, Fabiana Vercellino, Domenico Serino, Alessandro Orsini, Alice Bonuccelli, Irene Bagnasco, Amanda Papa, Carlo Minetti, Duccio Maria Cordelli, Pasquale Striano

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Acute Neurological Presentation in Children With SARS-CoV-2 Infection por Antonella Riva, Antonella Riva, Gianluca Piccolo, Gianluca Piccolo, Federica Balletti, Maria Binelli, Noemi Brolatti, Noemi Brolatti, Alberto Verrotti, Elisabetta Amadori, Elisabetta Amadori, Alberto Spalice, Thea Giacomini, Thea Giacomini, Maria Margherita Mancardi, Maria Margherita Mancardi, Paola Iannetti, Maria Stella Vari, Emanuela Piccotti, Pasquale Striano, Pasquale Striano, Giacomo Brisca

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Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders por Paola Borgia, Simona Baldassari, Nicoletta Pedemonte, Ebba Alkhunaizi, Gianluca D’Onofrio, Domenico Tortora, Elisa Calì, Paolo Scudieri, Ganna Balagura, Ilaria Musante, Maria Cristina Diana, Marina Pedemonte, Maria Stella Vari, Michele Iacomino, Antonella Riva, Roberto Chimenz, Giuseppe D. Mangano, Mohammad Hasan Mohammadi, Mehran Beiraghi Toosi, Farah Ashrafzadeh, Shima Imannezhad, Ehsan Ghayoor Karimiani, Andrea Accogli, Maria Cristina Schiaffino, Mohamad Maghnie, Miguel Angel Soler, Karl Echiverri, Charles K. Abrams, Pasquale Striano, Sara Fortuna, Reza Maroofian, Henry Houlden, Federico Zara, Chiara Fiorillo, Vincenzo Salpietro

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