Featured Articles
The following featured articles are from NICHD-supported researchers:
- Downs, J., Leonard, H., & Hill, K. (2012). Initial assessment of the StepWatch Activity Monitor™ to measure walking activity in Rett syndrome. Disability and Rehabilitation, 34, 1010–1015. PMID: 22107440
- Goffin, D., Allen, M., Zhang, L., Amorim, M., Wang, I. T., Reyes, A. R., et al. (2011). Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability, and ERP responses. Nature Neuroscience, 15, 274–283. PMID: 22119903
- Lane, J. B., Lee, H. S., Smith, L. W., Cheng, P., Percy, A. K., Glaze, D. G., et al. (2011). Clinical severity and quality of life in children and adolescents with Rett syndrome. Neurology, 77, 1812–1818. PMID: 22013176.
- McCauley, M. D., Wang, T., Mike, E., Herrera J., Beavers, D. L., Huang, T. W., et al. (2011). Pathogenesis of lethal cardiac arrhythmias in Mecp2 mutant mice: Implications for therapy in Rett syndrome. Science Translational Medicine, 3,113ra125. PMID 22174313
- McGraw, C. M., Samaco, R. C., & Zoghbi, H. Y. (2011). Adult neural function requires MeCP2. Science, 333, 186. PMID: 21636743
PubMed Search Results
Use the links below to search the PubMed database of more than 20 million citations for scientific articles with the keyword "Rett syndrome."
PubMed search results for NICHD articles with keyword "Rett syndrome" (and support from NICHD)
PubMed search results for all articles with keyword "Rett syndrome"