Search Results - Vignoli, Aglaia

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

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Cardiac asystoles misdiagnosed as epileptic seizures by Chiesa, Valentina, Vignoli, Aglaia, Canevini, Maria Paola

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Healthcare transition from childhood to adulthood in Tuberous Sclerosis Complex by Peron, Angela, Canevini, Maria Paola, Ghelma, Filippo, Di Marco, Fabiano, Vignoli, Aglaia

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SLC35F1 as a candidate gene for neurodevelopmental disorders resembling Rett syndrome by Di Fede, Elisabetta, Peron, Angela, Colombo, Elisa Adele, Gervasini, Cristina, Vignoli, Aglaia

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

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

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Phenotypes in adult patients with Rett syndrome: results of a 13-year experience and insights into healthcare transition by Peron, Angela, Canevini, Maria Paola, Ghelma, Filippo, Arancio, Rosangela, Savini, Miriam Nella, Vignoli, Aglaia

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Sleep in ring chromosome 20 syndrome: a peculiar electroencephalographic pattern by Zambrelli, Elena, Vignoli, Aglaia, Nobili, Lino, Didato, Giuseppe, Mastrangelo, Massimo, Turner, Katherine, Canevini, Maria Paola

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

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

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

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

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

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Epilepsy in adult patients with tuberous sclerosis complex by Vignoli, Aglaia, La Briola, Francesca, Turner, Katherine, Peron, Angela, Vannicola, Chiara, Chiesa, Valentina, Zambrelli, Elena, Bruschi, Fabio, Viganò, Ilaria, Canevini, Maria Paola

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Tuberous sclerosis complex (TSC), lymphangioleiomyomatosis, and COVID‐19: The experience of a TSC clinic in Italy by Peron, Angela, La Briola, Francesca, Bruschi, Fabio, Terraneo, Silvia, Vannicola, Chiara, Previtali, Roberto, Perazzoli, Sabrina, Morenghi, Emanuela, Bulfamante, Gaetano, Vignoli, Aglaia, Canevini, Maria Paola

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

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Genetic investigations on 8 patients affected by ring 20 chromosome syndrome by Giardino, Daniela, Vignoli, Aglaia, Ballarati, Lucia, Recalcati, Maria Paola, Russo, Silvia, Camporeale, Nicole, Marchi, Margherita, Finelli, Palma, Accorsi, Patrizia, Giordano, Lucio, La Briola, Francesca, Chiesa, Valentina, Canevini, Maria Paola, Larizza, Lidia

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

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KMT2A: Umbrella Gene for Multiple Diseases by Castiglioni, Silvia, Di Fede, Elisabetta, Bernardelli, Clara, Lettieri, Antonella, Parodi, Chiara, Grazioli, Paolo, Colombo, Elisa Adele, Ancona, Silvia, Milani, Donatella, Ottaviano, Emerenziana, Borghi, Elisa, Massa, Valentina, Ghelma, Filippo, Vignoli, Aglaia, Lesma, Elena, Gervasini, Cristina

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

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