Hasil Pencarian - Stella Vari

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  1. 1
    Todd Paralysis in Rolandic Epilepsy

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

    Diterbitkan 2015-07-01
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  2. 2
    Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus

    Impact and management of drooling in children with neurological disorders: an Italian Delphi consensus oleh 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

    Diterbitkan 2022-07-01
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  3. 3
    Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet.

    Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet. oleh 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

    Diterbitkan 2017-01-01
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  4. 4
    New Trends and Most Promising Therapeutic Strategies for Epilepsy Treatment

    New Trends and Most Promising Therapeutic Strategies for Epilepsy Treatment oleh 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

    Diterbitkan 2021-12-01
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  5. 5
    Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in <i>KCNA1</i> Impairing the Voltage Sensitivity of Kv1.1 Channel

    Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in <i>KCNA1</i> Impairing the Voltage Sensitivity of Kv1.1 Channel oleh 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

    Diterbitkan 2021-01-01
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  6. 6
    A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy

    A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy oleh 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

    Diterbitkan 2023-09-01
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  7. 7
    Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’ project

    Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’ project oleh 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

    Diterbitkan 2020-07-01
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  8. 8
    Acute Neurological Presentation in Children With SARS-CoV-2 Infection

    Acute Neurological Presentation in Children With SARS-CoV-2 Infection oleh 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

    Diterbitkan 2022-07-01
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  9. 9
    Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders

    Genotype–phenotype correlations and disease mechanisms in PEX13-related Zellweger spectrum disorders oleh 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

    Diterbitkan 2022-07-01
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