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

Rett syndrome (RTT) is a devastating neurodevelopmental disorder that affects one in ten thousand girls and has no cure. The majority of RTT patients display mutations in the gene that codes for the methyl-CpG-binding protein 2 (MeCP2). Clinical observations and neurobiological analysis of mouse mod...

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Veröffentlicht in:	Autism Research and Treatment 2012-01, Vol.2012 (2012), p.186-199
Hauptverfasser:	Scusa, Maria Flora, Pini, Giorgio, Congiu, Laura, Benincasa, Alberto, Morescalchi, Paolina, Bottiglioni, Ilaria, Di Marco, Pietro, Borelli, Paolo, Bonuccelli, Ubaldo, Della-Chiesa, Andrea, Prina-Mello, Adriele, Tropea, Daniela
Format:	Artikel
Sprache:	eng
Schlagworte:	Clinical Study
Online-Zugang:	Volltext
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