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

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NFIA haploinsufficiency: case series and literature review von Dini, Gianluca, Verrotti, Alberto, Gorello, Paolo, Soliani, Luca, Cordelli, Duccio Maria, Antona, Vincenzo, Mencarelli, Amedea, Colavito, Davide, Prontera, Paolo

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Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic Study von 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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IMU-based protocol for gait performance assessment in paediatric patients with rare neurological diseases von Bisi, Maria Cristina, Fetta, Anna, Soliani, Luca, Sperandeo, Federica, Utili, Anna, Cordelli, Duccio Maria, Stagni, Rita

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Diverse faces of GNAO1: mild forms in epilepsy and autism von Ludlam, William Grant, Soliani, Luca, Domínguez-Carral, Jana, Cordelli, Duccio Maria, Marchiani, Valentina, Gorría-Redondo, Nerea, Aguilera-Albesa, Sergio, Martemyanov, Kirill A., Ortigoza-Escobar, Juan Darío

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Status Epilepticus in Chromosomal Disorders Associated with Epilepsy: A Systematic Review von Bergonzini, Luca, Pruccoli, Jacopo, Pettenuzzo, Ilaria, Pugliano, Rosa, Soliani, Luca, Fetta, Anna, Cordelli, Duccio Maria

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Early-onset Dopamine Transporter Deficiency Syndrome: Long-term Follow-up von Baga, Margherita, Spagnoli, Carlotta, Soliani, Luca, Salerno, Grazia Gabriella, Rizzi, Susanna, Frattini, Daniele, Pisani, Francesco, Fusco, Carlo

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Paroxysmal movement disorder with response to carbamazepine in a patient with RHOBTB2 developmental and epileptic encephalopathy von Spagnoli, Carlotta, Soliani, Luca, Caraffi, Stefano Giuseppe, Baga, Margherita, Rizzi, Susanna, Salerno, Grazia Gabriella, Frattini, Daniele, Garavelli, Livia, Koskenvuo, Juha, Pisani, Francesco, Fusco, Carlo

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A Novel De Novo KIF21A Variant in a Patient With Congenital Fibrosis of the Extraocular Muscles With a Syndromic CFEOM Phenotype von Soliani, Luca, Spagnoli, Carlotta, Salerno, Grazia G., Mehine, Miika, Rizzi, Susanna, Frattini, Daniele, Koskenvuo, Juha, Fusco, Carlo

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Neurological Phenotype of Mowat-Wilson Syndrome von Cordelli, Duccio Maria, Di Pisa, Veronica, Fetta, Anna, Garavelli, Livia, Maltoni, Lucia, Soliani, Luca, Ricci, Emilia

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Long-term follow-up in infantile-onset SCAR18: A case report von Iodice, Alessandro, Spagnoli, Carlotta, Cangini, Margherita, Soliani, Luca, Rizzi, Susanna, Salerno, Grazia Gabriella, Frattini, Daniele, Pisani, Francesco, Fusco, Carlo

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Neuropsychological and behavioral disorders as presentation symptoms in two brothers with early-infantile Niemann-Pick type C von Soliani, Luca, Salerno, Grazia Gabriella, Pisani, Francesco, Barigazzi, Ilaria, Rizzi, Susanna, Spagnoli, Carlotta, Frattini, Daniele, Zangrandi, Andrea, Fusco, Carlo

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Aromatic L-Amino-Acid Decarboxylase Deficiency Screening by Analysis of 3-O-Methyldopa in Dried Blood Spots: Results of a Multicentric Study in Neurodevelopmental Disorders von Rizzi, Susanna, Spagnoli, Carlotta, Bellini, Melissa, Cesaroni, Carlo Alberto, Spezia, Elisabetta, Bergonzini, Patrizia, Caramaschi, Elisa, Soliani, Luca, Turco, Emanuela Claudia, Piccolo, Benedetta, Demuth, Laura, Cordelli, Duccio Maria, Biasucci, Giacomo, Frattini, Daniele, Fusco, Carlo

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Cognitive, Behavioral, and Sensory Profile of Pallister-Killian Syndrome: A Prospective Study of 22 Individuals von Fetta, Anna, Soliani, Luca, Trevisan, Alessia, Pugliano, Rosa, Ricci, Emilia, Di Pisa, Veronica, Pignataro, Veronica, Angotti, Marida, Rocca, Alessandro, Salce, Bianca, Mancardi, Maria Margherita, Giordano, Lucio, Pruna, Dario, Parmeggiani, Antonia, Cordelli, Duccio Maria

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Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature von Soliani, Luca, Alcalá San Martín, Adrián, Balsells, Sol, Hernando‐Davalillo, Cristina, Ortigoza‐Escobar, Juan Darío

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Paroxysmal Non‐Kinesigenic Dyskinesia: Utility of the Quantification of GLUT1 in Red Blood Cells von Soliani, Luca, Martorell, Loreto, Yubero, Delia, Verges, Carla, Petit, Vincent, Ortigoza‐Escobar, Juan Darío

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COMBING MACHINE WITH MEANS FOR CONTROLLING THE SPEED OF THE DETACHING ROLLERS von SOLIANI, Luca, VAVASSORI, Paolo

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COMBING MACHINE EQUIPPED WITH ORIENTATION MEANS FOR THE FIBERS OF THE EDGES OF THE FIBER WEB AND RELATED METHOD von SOLIANI, Luca, VAVASSORI, Paolo

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PETTINATRICE DOTATA DI MEZZI DI ORIENTAMENTO DELLE FIBRE DEI BORDI DEL VELO DI FIBRE E RELATIVO METODO von Soliani, Luca, Vavassori, Paolo

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COMBING MACHINE FOR A SPINNING PREPARATION LINE von PRANDINI, Girolamo, SOLIANI, Luca

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