Face perception and processing in early infancy: inborn predispositions and developmental changes

por Simion, Francesca, Giorgio, Elisa Di
Publicado 2015

Coherent Structure Formation through nonlinear interactions in 2D Magnetohydrodynamic Turbulence

por De Giorgio, Elisa, Servidio, Sergio, Veltri, Pierluigi
Publicado 2017

Newborns’ sensitivity to speed changes as a building block for animacy perception

por Di Giorgio, Elisa, Lunghi, Marco, Vallortigara, Giorgio, Simion, Francesca
Publicado 2021

Impact of the COVID-19 Italian Lockdown on the Physiological and Psychological Well-Being of Children with Fragile X Syndrome and Their Families

por Di Giorgio, Elisa, Polli, Roberta, Lunghi, Marco, Murgia, Alessandra
Publicado 2021

The interplay between mothers’ and children behavioral and psychological factors during COVID-19: an Italian study

por Di Giorgio, Elisa, Di Riso, Daniela, Mioni, Giovanna, Cellini, Nicola
Publicado 2020

Protein Stability Perturbation Contributes to the Loss of Function in Haploinsufficient Genes

por Birolo, Giovanni, Benevenuta, Silvia, Fariselli, Piero, Capriotti, Emidio, Giorgio, Elisa, Sanavia, Tiziana
Publicado 2021

Difference in Visual Social Predispositions Between Newborns at Low- and High-risk for Autism

por Di Giorgio, Elisa, Frasnelli, Elisa, Rosa Salva, Orsola, Maria Luisa, Scattoni, Puopolo, Maria, Tosoni, Daniela, Simion, Francesca, Vallortigara, Giorgio
Publicado 2016

Corrigendum: Difference in Visual Social Predispositions Between Newborns at Low- and High-risk for Autism

por Di Giorgio, Elisa, Frasnelli, Elisa, Rosa Salva, Orsola, Scattoni, Maria Luisa, Puopolo, Maria, Tosoni, Daniela, Simion, Francesca, Vallortigara, Giorgio
Publicado 2016

Abnormal visual attention to simple social stimuli in 4-month-old infants at high risk for Autism

por Di Giorgio, Elisa, Rosa-Salva, Orsola, Frasnelli, Elisa, Calcagnì, Antonio, Lunghi, Marco, Scattoni, Maria Luisa, Simion, Francesca, Vallortigara, Giorgio
Publicado 2021

O056. Migraine as presenting symptom of SLC20A2gene mutations

por Rubino, Elisa, Giorgio, Elisa, Rainero, Innocenzo, Ferrero, Patrizia, Gallone, Salvatore, Govone, Flora, Pinessi, Lorenzo, Orsi, Laura, Duca, Sergio, Brusco, Alfredo
Publicado 2015

Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: case report of an Italian patient

por Piro, Ettore, Serra, Gregorio, Antona, Vincenzo, Giuffrè, Mario, Giorgio, Elisa, Sirchia, Fabio, Schierz, Ingrid Anne Mandy, Brusco, Alfredo, Corsello, Giovanni
Publicado 2020

Analysis of the DNA methylation pattern of the promoter region of calcitonin gene-related peptide 1 gene in patients with episodic migraine: An exploratory case-control study

por Rubino, Elisa, Boschi, Silvia, Giorgio, Elisa, Pozzi, Elisa, Marcinnò, Andrea, Gallo, Erica, Roveta, Fausto, Grassini, Alberto, Brusco, Alfredo, Rainero, Innocenzo
Publicado 2022

Prenatal findings of cataract and arthrogryposis: recurrence of cerebro-oculo-facio-skeletal syndrome and review of differential diagnosis

por Sirchia, Fabio, Fantasia, Ilaria, Feresin, Agnese, Giorgio, Elisa, Faletra, Flavio, Mordeglia, Denise, Barbieri, Moira, Guida, Valentina, De Luca, Alessandro, Stampalija, Tamara
Publicado 2021

High miR-100 expression is associated with aggressive features and modulates TORC1 complex activation in lung carcinoids

por Rapa, Ida, Votta, Arianna, Gatti, Gaia, Izzo, Stefania, Buono, Nicola Lo, Giorgio, Elisa, Vatrano, Simona, Napoli, Francesca, Scarpa, Aldo, Scagliotti, Giorgio, Papotti, Mauro, Volante, Marco
Publicado 2018

Understanding the Ultra-Rare Disease Autosomal Dominant Leukodystrophy: an Updated Review on Morpho-Functional Alterations Found in Experimental Models

por Neri, Irene, Ramazzotti, Giulia, Mongiorgi, Sara, Rusciano, Isabella, Bugiani, Marianna, Conti, Luciano, Cousin, Margot, Giorgio, Elisa, Padiath, Quasar S., Vaula, Giovanna, Cortelli, Pietro, Manzoli, Lucia, Ratti, Stefano
Publicado 2023

Messenger RNA processing is altered in autosomal dominant leukodystrophy(†)

por Bartoletti-Stella, Anna, Gasparini, Laura, Giacomini, Caterina, Corrado, Patrizia, Terlizzi, Rossana, Giorgio, Elisa, Magini, Pamela, Seri, Marco, Baruzzi, Agostino, Parchi, Piero, Brusco, Alfredo, Cortelli, Pietro, Capellari, Sabina
Publicado 2015

Messenger RNA processing is altered in autosomal dominant leukodystrophy

por Bartoletti-Stella, Anna, Gasparini, Laura, Giacomini, Caterina, Corrado, Patrizia, Terlizzi, Rossana, Giorgio, Elisa, Magini, Pamela, Seri, Marco, Baruzzi, Agostino, Parchi, Piero, Brusco, Alfredo, Cortelli, Pietro, Capellari, Sabina
Publicado 2017

Lamin B1 as a key modulator of the developing and aging brain

por Koufi, Foteini-Dionysia, Neri, Irene, Ramazzotti, Giulia, Rusciano, Isabella, Mongiorgi, Sara, Marvi, Maria Vittoria, Fazio, Antonietta, Shin, Minkyung, Kosodo, Yoichi, Cani, Ilaria, Giorgio, Elisa, Cortelli, Pietro, Manzoli, Lucia, Ratti, Stefano
Publicado 2023

A Novel CCT5 Missense Variant Associated with Early Onset Motor Neuropathy

por Antona, Vincenzo, Scalia, Federica, Giorgio, Elisa, Radio, Francesca C., Brusco, Alfredo, Oliveri, Massimiliano, Corsello, Giovanni, Lo Celso, Fabrizio, Vadalà, Maria, Conway de Macario, Everly, Macario, Alberto J. L., Cappello, Francesco, Giuffrè, Mario
Publicado 2020

Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy

por Nmezi, Bruce, Giorgio, Elisa, Raininko, Raili, Lehman, Anna, Spielmann, Malte, Koenig, Mary Kay, Adejumo, Rahmat, Knight, Melissa, Gavrilova, Ralitza, Alturkustani, Murad, Sharma, Manas, Hammond, Robert, Gahl, William A., Toro, Camilo, Brusco, Alfredo, Padiath, Quasar S.
Publicado 2019