Rett syndrome is a severe neurological developmental disorder. In this syndrome, the high incidence of sudden death is correlated with an alteration of ventricular repolarization. The purpose of this study was to evaluate plasmatic levels of nerve growth factor (NGF) in Rett patients with prolonged corrected QT (QTc) interval in comparison with those of Rett patients with normal QTc. We observed 23 female Rett patients (9.9+/-4.7 years). NGF plasma levels and QTc interval were measured in all patients. Student t-test was performed for statistical analysis. NGF plasma levels were significantly lower in Rett patients with QTc interval prolongation (QTc > 0.44 sec) in comparison with Rett patients with a normal QTc interval (4.5+/-4.5 vs 11+/-...
Aims: Rett syndrome (RTT) is a rare neurodevelopmental disorder frequently linked to methyl-CpG-bind...
AIMS: Rett syndrome (RTT) is a rare neurodevelopmental disorder frequently linked to methyl-CpG-bind...
A role for neurotrophic factors has been postulated in some human neurodegenerative disorders such a...
Rett syndrome is a severe neurological developmental disorder. In this syndrome, the high incidence ...
Rett syndrome is a severe neurodevelop-mental disorder of unknown aetiology. A prolonged QT interval...
BACKGROUND: In Rett syndrome the autonomic nervous system is abnormal at various levels, from the c...
Rett syndrome (RS) is a genetic disorder predominant in females, with sudden death (SD), thought to ...
Incidence of sudden death in Rett syndrome is greater than that of the general population, and cardi...
Incidence of sudden death in Rett syndrome is greater than that of the general population and cardia...
Incidence of sudden death in Rett syndrome is greater than that of the general population, and cardi...
Rett syndrome (RTT) is a severe developmental-neurological disorder, characterized by profound and p...
The incidence of sudden death in Rett syndrome is greater than that of the general population. Previ...
Many studies have attempted to establish the genotype-phenotype correlation in Rett syndrome (RTT). ...
Aims: Rett syndrome (RTT) is a rare neurodevelopmental disorder frequently linked to methyl-CpG-bind...
AIMS: Rett syndrome (RTT) is a rare neurodevelopmental disorder frequently linked to methyl-CpG-bind...
A role for neurotrophic factors has been postulated in some human neurodegenerative disorders such a...
Rett syndrome is a severe neurological developmental disorder. In this syndrome, the high incidence ...
Rett syndrome is a severe neurodevelop-mental disorder of unknown aetiology. A prolonged QT interval...
BACKGROUND: In Rett syndrome the autonomic nervous system is abnormal at various levels, from the c...
Rett syndrome (RS) is a genetic disorder predominant in females, with sudden death (SD), thought to ...
Incidence of sudden death in Rett syndrome is greater than that of the general population, and cardi...
Incidence of sudden death in Rett syndrome is greater than that of the general population and cardia...
Incidence of sudden death in Rett syndrome is greater than that of the general population, and cardi...
Rett syndrome (RTT) is a severe developmental-neurological disorder, characterized by profound and p...
The incidence of sudden death in Rett syndrome is greater than that of the general population. Previ...
Many studies have attempted to establish the genotype-phenotype correlation in Rett syndrome (RTT). ...
Aims: Rett syndrome (RTT) is a rare neurodevelopmental disorder frequently linked to methyl-CpG-bind...
AIMS: Rett syndrome (RTT) is a rare neurodevelopmental disorder frequently linked to methyl-CpG-bind...
A role for neurotrophic factors has been postulated in some human neurodegenerative disorders such a...