Hasil Pencarian - Aglaia Vignoli

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  1. 1
    Rett Syndrome and Other Neurodevelopmental Disorders Share Common Changes in Gut Microbial Community: A Descriptive Review

    Rett Syndrome and Other Neurodevelopmental Disorders Share Common Changes in Gut Microbial Community: A Descriptive Review oleh Elisa Borghi, Aglaia Vignoli

    Diterbitkan 2019-08-01
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  2. 2
    Is Gut Microbiota a Key Player in Epilepsy Onset? A Longitudinal Study in Drug-Naive Children

    Is Gut Microbiota a Key Player in Epilepsy Onset? A Longitudinal Study in Drug-Naive Children oleh Camilla Ceccarani, Ilaria Viganò, Emerenziana Ottaviano, Maria Gaia Redaelli, Marco Severgnini, Aglaia Vignoli, Aglaia Vignoli, Elisa Borghi

    Diterbitkan 2021-12-01
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  3. 3
    Late onset myoclonic epilepsy in Down syndrome and dementia

    Late onset myoclonic epilepsy in Down syndrome and dementia oleh Annapia Verri, Aglaia Vignoli, Michele Terzaghi, Valeria Destefani, Luigi Nespoli

    Diterbitkan 2012-09-01
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  4. 4
    Parents’ satisfaction of tele-rehabilitation for children with neurodevelopmental disabilities during the COVID-19 pandemic

    Parents’ satisfaction of tele-rehabilitation for children with neurodevelopmental disabilities during the COVID-19 pandemic oleh Pamela Frigerio, Liliana Del Monte, Aurora Sotgiu, Costantino De Giacomo, Aglaia Vignoli

    Diterbitkan 2022-06-01
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  5. 5
    Gut microbiota profile in CDKL5 deficiency disorder patients

    Gut microbiota profile in CDKL5 deficiency disorder patients oleh Elisa Borghi, Ornella Xynomilakis, Emerenziana Ottaviano, Camilla Ceccarani, Ilaria Viganò, Paola Tognini, Aglaia Vignoli

    Diterbitkan 2024-03-01
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  6. 6
    Rett Syndrome: A Focus on Gut Microbiota

    Rett Syndrome: A Focus on Gut Microbiota oleh Elisa Borghi, Francesca Borgo, Marco Severgnini, Miriam Nella Savini, Maria Cristina Casiraghi, Aglaia Vignoli

    Diterbitkan 2017-02-01
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  7. 7
    Living with Epilepsy in Adolescence in Italy: Psychological and Behavioral Impact

    Living with Epilepsy in Adolescence in Italy: Psychological and Behavioral Impact oleh Katherine Turner, Francesca La Briola, Aglaia Vignoli, Elena Zambrelli, Valentina Chiesa, Laura Fongoni, Olivia Baldi, Maria Paola Canevini

    Diterbitkan 2023-02-01
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  8. 8
    Effects of Combined Transcranial Direct Current Stimulation with Cognitive Training in Girls with Rett Syndrome

    Effects of Combined Transcranial Direct Current Stimulation with Cognitive Training in Girls with Rett Syndrome oleh Rosa Angela Fabio, Antonio Gangemi, Martina Semino, Aglaia Vignoli, Alberto Priori, Maria Paola Canevini, Gabriella Di Rosa, Tindara Caprì

    Diterbitkan 2020-05-01
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  9. 9
    The TAND checklist: a useful screening tool in children with tuberous sclerosis and neurofibromatosis type 1

    The TAND checklist: a useful screening tool in children with tuberous sclerosis and neurofibromatosis type 1 oleh Francesca Cervi, Veronica Saletti, Katherine Turner, Angela Peron, Sara Bulgheroni, Matilde Taddei, Francesca La Briola, Maria Paola Canevini, Aglaia Vignoli

    Diterbitkan 2020-09-01
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  10. 10
    Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes

    Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes oleh Angela Peron, Angela Peron, Angela Peron, Ilaria Catusi, Maria Paola Recalcati, Luciano Calzari, Lidia Larizza, Aglaia Vignoli, Maria Paola Canevini

    Diterbitkan 2020-12-01
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  11. 11
    Early diagnosis of tuberous sclerosis complex: a race against time. How to make the diagnosis before seizures?

    Early diagnosis of tuberous sclerosis complex: a race against time. How to make the diagnosis before seizures? oleh Monika Słowińska, Sergiusz Jóźwiak, Angela Peron, Julita Borkowska, Dariusz Chmielewski, Krzysztof Sadowski, Elżbieta Jurkiewicz, Aglaia Vignoli, Francesca La Briola, Maria Paola Canevini, Katarzyna Kotulska-Jóźwiak

    Diterbitkan 2018-01-01
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  12. 12
    Modeling RTT Syndrome by iPSC-Derived Neurons from Male and Female Patients with Heterogeneously Severe Hot-Spot MECP2 Variants

    Modeling RTT Syndrome by iPSC-Derived Neurons from Male and Female Patients with Heterogeneously Severe Hot-Spot MECP2 Variants oleh Sara Perego, Valentina Alari, Gianluca Pietra, Andrea Lamperti, Alessandro Vimercati, Nicole Camporeale, Maria Garzo, Francesca Cogliati, Donatella Milani, Aglaia Vignoli, Angela Peron, Lidia Larizza, Tommaso Pizzorusso, Silvia Russo

    Diterbitkan 2022-11-01
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  13. 13
    Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies

    Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies oleh Chiara Parodi, Elisabetta Di Fede, Angela Peron, Angela Peron, Angela Peron, Ilaria Viganò, Paolo Grazioli, Silvia Castiglioni, Richard H. Finnell, Cristina Gervasini, Cristina Gervasini, Aglaia Vignoli, Valentina Massa, Valentina Massa

    Diterbitkan 2021-04-01
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  14. 14
    Myoclonus: Differential diagnosis and current management

    Myoclonus: Differential diagnosis and current management oleh Antonella Riva, Gianluca D'Onofrio, Edoardo Ferlazzo, Angelo Pascarella, Elena Pasini, Silvana Franceschetti, Ferruccio Panzica, Laura Canafoglia, Aglaia Vignoli, Antonietta Coppola, Valeria Badioni, Francesca Beccaria, Angelo Labate, Antonio Gambardella, Antonino Romeo, Giuseppe Capovilla, Roberto Michelucci, Pasquale Striano, Vincenzo Belcastro

    Diterbitkan 2024-04-01
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  15. 15
    Pathogenic Variants in <i>STXBP1</i> and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes

    Pathogenic Variants in <i>STXBP1</i> and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes oleh Francesca Cogliati, Valentina Giorgini, Maura Masciadri, Maria Teresa Bonati, Margherita Marchi, Irene Cracco, Davide Gentilini, Angela Peron, Miriam Nella Savini, Luigina Spaccini, Barbara Scelsa, Silvia Maitz, Edvige Veneselli, Giulia Prato, Maria Pintaudi, Isabella Moroni, Aglaia Vignoli, Lidia Larizza, Silvia Russo

    Diterbitkan 2019-07-01
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  16. 16
    Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study

    Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study oleh Benedetta Cavirani, Carlotta Spagnoli, Stefano Giuseppe Caraffi, Anna Cavalli, Carlo Alberto Cesaroni, Gianni Cutillo, Valentina De Giorgis, Daniele Frattini, Giulia Bruna Marchetti, Silvia Masnada, Angela Peron, Susanna Rizzi, Costanza Varesio, Luigina Spaccini, Aglaia Vignoli, Maria Paola Canevini, Pierangelo Veggiotti, Livia Garavelli, Carlo Fusco

    Diterbitkan 2024-01-01
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  17. 17
    Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic Study

    Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic Study oleh Anna Fetta, Anna Fetta, Veronica Di Pisa, Martina Ruscelli, Luca Soliani, Luca Soliani, Giacomo Sperti, Sara Ubertiello, Emilia Ricci, Greta Mainieri, Alessandro Rocca, Maria Margherita Mancardi, Lucio Giordano, Dario Pruna, Aglaia Vignoli, Federica Provini, Federica Provini, Duccio Maria Cordelli, Duccio Maria Cordelli

    Diterbitkan 2021-12-01
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  18. 18
    Mapping the Effect of Interictal Epileptic Activity Density During Wakefulness on Brain Functioning in Focal Childhood Epilepsies With Centrotemporal Spikes

    Mapping the Effect of Interictal Epileptic Activity Density During Wakefulness on Brain Functioning in Focal Childhood Epilepsies With Centrotemporal Spikes oleh Anna Elisabetta Vaudano, Anna Elisabetta Vaudano, Pietro Avanzini, Gaetano Cantalupo, Melissa Filippini, Andrea Ruggieri, Andrea Ruggieri, Francesca Talami, Elisa Caramaschi, Patrizia Bergonzini, Aglaia Vignoli, Pierangelo Veggiotti, Azzura Guerra, Giuliana Gessaroli, Margherita Santucci, Maria Paola Canevini, Benedetta Piccolo, Francesco Pisani, Giuseppe Gobbi, Bernardo Dalla Bernardina, Stefano Meletti, Stefano Meletti

    Diterbitkan 2019-12-01
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  19. 19
    P267: TSC1/TSC2 mosaicism is found in ∼13% of individuals with tuberous sclerosis and is associated with a distinctive phenotypic severity

    P267: TSC1/TSC2 mosaicism is found in ∼13% of individuals with tuberous sclerosis and is associated with a distinctive phenotypic severity oleh Angela Peron, Rosa Maria Alfano, Barry Moore, Mark Nellist, Brent Pedersen, Francesca La Briola, Luigina Spaccini, Federica Natacci, Maria Paola Recalcati, Valentina Chiesa, Rosangela Arancio, Ugo Cavallari, Chiara Vannicola, Graziella Cefalo, Silvia Maitz, Stefania Bigoni, Lorenzo Gualandri, Cristina Gervasini, Pierangelo Veggiotti, Wilfred van Ijcken, Aglaia Vignoli, Gaetano Pietro Bulfamante, John Carey, Maria Paola Canevini

    Diterbitkan 2023-01-01
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  20. 20
    Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children

    Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children oleh Anna Fetta, Francesco Toni, Ilaria Pettenuzzo, Emilia Ricci, Alessandro Rocca, Caterina Gambi, Luca Soliani, Veronica Di Pisa, Silvia Martini, Giacomo Sperti, Valeria Cagnazzo, Patrizia Accorsi, Emanuele Bartolini, Domenica Battaglia, Pia Bernardo, Maria Paola Canevini, Anna Rita Ferrari, Lucio Giordano, Chiara Locatelli, Margherita Mancardi, Alessandro Orsini, Tommaso Pippucci, Dario Pruna, Anna Rosati, Agnese Suppiej, Sara Tagliani, Alessandro Vaisfeld, Aglaia Vignoli, Kosuke Izumi, Ian Krantz, Duccio Maria Cordelli

    Diterbitkan 2024-03-01
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