Resultados de búsqueda - Roberta Polli

Identification of SETBP1 Mutations by Gene Panel Sequencing in Individuals With Intellectual Disability or With “Developmental and Epileptic Encephalopathy” por Emanuela Leonardi, Emanuela Leonardi, Elisa Bettella, Elisa Bettella, Maria Federica Pelizza, Maria Cristina Aspromonte, Maria Cristina Aspromonte, Roberta Polli, Roberta Polli, Clementina Boniver, Stefano Sartori, Donatella Milani, Alessandra Murgia, Alessandra Murgia

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A Supervised Classification of Children with Fragile X Syndrome and Controls Based on Kinematic and sEMG Parameters por Weronika Joanna Piatkowska, Fabiola Spolaor, Marco Romanato, Roberta Polli, Alessandra Huang, Alessandra Murgia, Zimi Sawacha

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Feasibility and Reliability Assessment of Video-Based Motion Analysis and Surface Electromyography in Children with Fragile X during Gait por Zimi Sawacha, Fabiola Spolaor, Weronika Joanna Piątkowska, Federica Cibin, Alfredo Ciniglio, Annamaria Guiotto, Marco Ricca, Roberta Polli, Alessandra Murgia

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Activation Ratio Correlates with IQ in Female Carriers of the <i>FMR1</i> Premutation por Dragana Protic, Roberta Polli, Ye Hyun Hwang, Guadalupe Mendoza, Randi Hagerman, Blythe Durbin-Johnson, Bruce E. Hayward, Karen Usdin, Alessandra Murgia, Flora Tassone

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