Clinical and genetic Rett syndrome variants are defined by stable electrophysiological profiles

por Keogh, Conor, Pini, Giorgio, Dyer, Adam H., Bigoni, Stefania, DiMarco, Pietro, Gemo, Ilaria, Reilly, Richard, Tropea, Daniela
Publicado 2018

IGF1 as a Potential Treatment for Rett Syndrome: Safety Assessment in Six Rett Patients

por Pini, Giorgio, Scusa, Maria Flora, Congiu, Laura, Benincasa, Alberto, Morescalchi, Paolina, Bottiglioni, Ilaria, Di Marco, Pietro, Borelli, Paolo, Bonuccelli, Ubaldo, Della-Chiesa, Andrea, Prina-Mello, Adriele, Tropea, Daniela
Publicado 2012

Illness Severity, Social and Cognitive Ability, and EEG Analysis of Ten Patients with Rett Syndrome Treated with Mecasermin (Recombinant Human IGF-1)

por Pini, Giorgio, Congiu, Laura, Benincasa, Alberto, DiMarco, Pietro, Bigoni, Stefania, Dyer, Adam H., Mortimer, Niall, Della-Chiesa, Andrea, O'Leary, Sean, McNamara, Rachel, Mitchell, Kevin J., Gill, Michael, Tropea, Daniela
Publicado 2016