Add to ORKGCopyright © 2014 Anna Maria Papini et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Rett syndrome (RTT), a neurodevelopmental disorder affecting exclusively (99%) female infants, is associated with loss-of-function mutations in the gene encodingmethyl-CpG binding protein 2 (MECP2) and, more rarely, cyclin-dependent kinase-like 5 (CDKL5) and forkhead box protein G1 (FOXG1). In this study, we aimed to evaluate the function of the immune system by measuring serum immunoglobulins (IgG and IgM) in RTT patients
Objectives: Rett syndrome (RTT) is a rare disorder causing severe intellectual and physical disabili...
Objective: Rett syndrome (RTT) is a neurological disorder and a leading cause of mental retardation ...
Rett syndrome (RTT) is a severe neurodevelopmental disorder associated with mutations in the X-linke...
Rett syndrome (RTT), a neurodevelopmental disorder affecting exclusively (99%) female infants, is as...
International audienceRett syndrome (RTT), a neurodevelopmental disorder affecting exclusively (99%)...
Copyright © 2015 Silvia Leoncini et al. This is an open access article distributed under the Creativ...
Rett syndrome (RTT) is a devastating neurodevelopmental disease, previously included into the autist...
Copyright © 2013 Alessio Cortelazzo et al. This is an open access article distributed under the Crea...
Copyright © 2012 Giorgio Pini et al. This is an open access article distributed under the Creative C...
Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder affecting almost exclusively gi...
Rett syndrome is a neurodevelopmental disorder characterized by cognitive and adaptive regression wi...
Copyright © 2014 Cinzia Signorini et al.This is an open access article distributed under theCreative...
The purpose of this research project is to compose a comprehensive timeline on the rare disease Rett...
The topic of this PhD thesis is the Rett syndrome (RTT, OMIM 312750), an X-linked neurodevelopmental...
Rett syndrome (RTT) is an X-linked progressive neurodevelopmental disorder causing mental retardatio...
Objectives: Rett syndrome (RTT) is a rare disorder causing severe intellectual and physical disabili...
Objective: Rett syndrome (RTT) is a neurological disorder and a leading cause of mental retardation ...
Rett syndrome (RTT) is a severe neurodevelopmental disorder associated with mutations in the X-linke...
Rett syndrome (RTT), a neurodevelopmental disorder affecting exclusively (99%) female infants, is as...
International audienceRett syndrome (RTT), a neurodevelopmental disorder affecting exclusively (99%)...
Copyright © 2015 Silvia Leoncini et al. This is an open access article distributed under the Creativ...
Rett syndrome (RTT) is a devastating neurodevelopmental disease, previously included into the autist...
Copyright © 2013 Alessio Cortelazzo et al. This is an open access article distributed under the Crea...
Copyright © 2012 Giorgio Pini et al. This is an open access article distributed under the Creative C...
Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder affecting almost exclusively gi...
Rett syndrome is a neurodevelopmental disorder characterized by cognitive and adaptive regression wi...
Copyright © 2014 Cinzia Signorini et al.This is an open access article distributed under theCreative...
The purpose of this research project is to compose a comprehensive timeline on the rare disease Rett...
The topic of this PhD thesis is the Rett syndrome (RTT, OMIM 312750), an X-linked neurodevelopmental...
Rett syndrome (RTT) is an X-linked progressive neurodevelopmental disorder causing mental retardatio...
Objectives: Rett syndrome (RTT) is a rare disorder causing severe intellectual and physical disabili...
Objective: Rett syndrome (RTT) is a neurological disorder and a leading cause of mental retardation ...
Rett syndrome (RTT) is a severe neurodevelopmental disorder associated with mutations in the X-linke...