Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

772 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Feeding experiences and growth status in a Rett syndrome population.
Oddy WH, Webb KG, Baikie G, Thompson SM, Reilly S, Fyfe SD, Young D, Anderson AM, Leonard H. Oddy WH, et al. Among authors: reilly s. J Pediatr Gastroenterol Nutr. 2007 Nov;45(5):582-90. doi: 10.1097/MPG.0b013e318073cbf7. J Pediatr Gastroenterol Nutr. 2007. PMID: 18030237
Development of a video-based evaluation tool in Rett syndrome.
Fyfe S, Downs J, McIlroy O, Burford B, Lister J, Reilly S, Laurvick CL, Philippe C, Msall M, Kaufmann WE, Ellaway C, Leonard H. Fyfe S, et al. Among authors: reilly s. J Autism Dev Disord. 2007 Oct;37(9):1636-46. doi: 10.1007/s10803-006-0293-9. Epub 2006 Dec 16. J Autism Dev Disord. 2007. PMID: 17180458
Towards a behavioral phenotype for Rett syndrome.
Mount RH, Hastings RP, Reilly S, Cass H, Charman T. Mount RH, et al. Among authors: reilly s. Am J Ment Retard. 2003 Jan;108(1):1-12. doi: 10.1352/0895-8017(2003)108<0001:TABPFR>2.0.CO;2. Am J Ment Retard. 2003. PMID: 12475362
Regression in individuals with Rett syndrome.
Charman T, Cass H, Owen L, Wigram T, Slonims V, Weeks L, Wisbeach A, Reilly S. Charman T, et al. Among authors: reilly s. Brain Dev. 2002 Aug;24(5):281-3. doi: 10.1016/s0387-7604(02)00058-x. Brain Dev. 2002. PMID: 12142064
Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndrome.
Charman T, Neilson TC, Mash V, Archer H, Gardiner MT, Knudsen GP, McDonnell A, Perry J, Whatley SD, Bunyan DJ, Ravn K, Mount RH, Hastings RP, Hulten M, Orstavik KH, Reilly S, Cass H, Clarke A, Kerr AM, Bailey ME. Charman T, et al. Among authors: reilly s. Eur J Hum Genet. 2005 Oct;13(10):1121-30. doi: 10.1038/sj.ejhg.5201471. Eur J Hum Genet. 2005. PMID: 16077736
Diversity of participation in children with cerebral palsy.
Imms C, Reilly S, Carlin J, Dodd K. Imms C, et al. Among authors: reilly s. Dev Med Child Neurol. 2008 May;50(5):363-9. doi: 10.1111/j.1469-8749.2008.02051.x. Epub 2008 Mar 18. Dev Med Child Neurol. 2008. PMID: 18355337 Free article.
772 results