Search Results - "RETT-SYNDROME"

A preliminary study on use of anticonvulsants and risk of fracture in Rett syndrome by Jian, Le, Bebbington, A., Downs, Jennepher, Jacoby, P., Leonard, H.

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Assessment and Management of Nutrition and Growth in Rett Syndrome by Leonard, H., Ravikumara, M., Baikie, G., Naseem, N., Ellaway, C., Percy, A., Abraham, S., Geerts, S., Lane, J., Jones, M., Bathgate, Katherine, Downs, J.

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Perspectives on hand function in girls and women with Rett syndrome by Downs, Jennepher, Parkinson, Stephanie, Ranelli, Sonia, Leonard, H., Diener, P., Lotan, M.

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Barriers to diagnosis of a rare neurological disorder in China - Lived experiences of Rett Syndrome families by Lim, F., Downs, Jennepher, Li, Jianghong, Bao, X., Leonard, H.

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Twenty years of surveillance in Rett syndrome: what does this tell us? by Anderson, A., Wong, K., Jacoby, P., Downs, Jennepher, Leonard, H.

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Early development and regression in Rett Syndrome by Lee, J.Y.L., Leonard, H., Piek, Jan Patricia, Downs, Jennepher

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Impact of scoliosis surgery on activites of daily living in females with Rett Syndrome by Downs, Jennepher, Young, D., De Klerk, N., Bebbington, A., Baikie, G., Leonard, H.

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Longitudinal hand function in Rett syndrome by Downs, Jennepher, Bebbington, A., Kaufmann, W., Leonard, H.

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Caring for a child with severe intellectual disability in China: The example of Rett syndrome by Lim, Faye, Downs, Jennepher, Li, Jianghong, Bao, Xinhua, Leonard, Helen

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Community Participation for Girls and Women Living with Rett Syndrome by Andrews, J., Leonard, H., Hammond, G., Girdler, Sonya, Rajapaksa, R., Bathgate, Katherine, Downs, J.

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p.R270X MECP2 mutation and mortality in Rett syndrome by Jian, Le, Archer, H., Ravine, D., Kerr, A., De Klerk, N., Christodoulou, J., Bailey, M.

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Atypical Presentations and Specific Genotypes Are Associated With a Delay in Diagnosis in Females With Rett Syndrome by Fehr, S., Downs, Jennepher, Bebbington, A., Leonard, H.

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Seizures in rett syndrom: An overview from a one-year calendar study by Jian, Le, Nagarajan, L., De Klerk, N., Ravine, D., Christodoulou, J., Leonard, H.

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The imprinted gene and parent-of-origin effect database now includes parental origin of de novo mutations. by Glaser, R.L., Ramsay, Josh, Morison, I.M.

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Using directed-content analysis to identify a framework for understanding quality of life in adults with Rett syndrome by Strugnell, A., Leonard, H., Epstein, A., Downs, Jennepher

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Determinants of sleep problems in children with intellectual disability by Gilbertson, M., Richardson, C., Eastwood, Peter, Wilson, A., Jacoby, P., Leonard, H., Downs, Jennepher

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