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Rett syndrome (RTT) is caused by mutations in the transcriptional repressor methyl CpG-binding protein 2 (MECP2).
Accurate measurement of dietary intake is essential for understanding the long-term effects of adolescent diet on chronic disease risk.
Few studies have examined the dietary patterns of adolescents and the social and environmental factors that may affect them during this life stage.
This study uses data from a large international database, InterRett, to examine genotype-phenotype relationships and compares these with previous findings in...
This study investigated the nature and prevalence of atypical pain responses in Rett syndrome and their relationships with specific MECP2 mutations.
Physical and mental health in mothers of children with Down syndrome.
Infection accounts for the majority of pediatric mortality and morbidity in developing countries, but there are limited data on the infectious diseases...
Rett syndrome (RTT) is an X-linked dominant neurodevelopmental disorder that is usually associated with mutations in the MECP2 gene.
To examine the prevalence, cumulative incidence, and survival in an Australian cohort with Rett syndrome (RTT).
Overweight and other risk factors for cardiovascular disease (CVD) as well as their clustering, are increasingly prevalent among adolescents.