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

67 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Evaluating Sleep Disturbances in Children With Rare Genetic Neurodevelopmental Syndromes.
Veatch OJ, Malow BA, Lee HS, Knight A, Barrish JO, Neul JL, Lane JB, Skinner SA, Kaufmann WE, Miller JL, Driscoll DJ, Bird LM, Butler MG, Dykens EM, Gold JA, Kimonis V, Bacino CA, Tan WH, Kothare SV, Peters SU, Percy AK, Glaze DG. Veatch OJ, et al. Among authors: lane jb. Pediatr Neurol. 2021 Oct;123:30-37. doi: 10.1016/j.pediatrneurol.2021.07.009. Epub 2021 Jul 24. Pediatr Neurol. 2021. PMID: 34388423 Free PMC article.
Rett syndrome: 1H spectroscopic imaging at 4.1 Tesla.
Pan JW, Lane JB, Hetherington H, Percy AK. Pan JW, et al. Among authors: lane jb. J Child Neurol. 1999 Aug;14(8):524-8. doi: 10.1177/088307389901400808. J Child Neurol. 1999. PMID: 10456763
Rett syndrome: clinical and molecular update.
Percy AK, Lane JB. Percy AK, et al. Among authors: lane jb. Curr Opin Pediatr. 2004 Dec;16(6):670-7. doi: 10.1097/01.mop.0000143693.59408.ce. Curr Opin Pediatr. 2004. PMID: 15548931 Review.
Rett syndrome: model of neurodevelopmental disorders.
Percy AK, Lane JB. Percy AK, et al. Among authors: lane jb. J Child Neurol. 2005 Sep;20(9):718-21. doi: 10.1177/08830738050200090301. J Child Neurol. 2005. PMID: 16225824 Review.
Early progressive encephalopathy in boys and MECP2 mutations.
Kankirawatana P, Leonard H, Ellaway C, Scurlock J, Mansour A, Makris CM, Dure LS 4th, Friez M, Lane J, Kiraly-Borri C, Fabian V, Davis M, Jackson J, Christodoulou J, Kaufmann WE, Ravine D, Percy AK. Kankirawatana P, et al. Neurology. 2006 Jul 11;67(1):164-6. doi: 10.1212/01.wnl.0000223318.28938.45. Neurology. 2006. PMID: 16832102
Rett syndrome: North American database.
Percy AK, Lane JB, Childers J, Skinner S, Annese F, Barrish J, Caeg E, Glaze DG, MacLeod P. Percy AK, et al. Among authors: lane jb. J Child Neurol. 2007 Dec;22(12):1338-41. doi: 10.1177/0883073807308715. J Child Neurol. 2007. PMID: 18174548
A study of the treatment of Rett syndrome with folate and betaine.
Glaze DG, Percy AK, Motil KJ, Lane JB, Isaacs JS, Schultz RJ, Barrish JO, Neul JL, O'Brien WE, Smith EO. Glaze DG, et al. Among authors: lane jb. J Child Neurol. 2009 May;24(5):551-6. doi: 10.1177/0883073808327827. Epub 2009 Feb 18. J Child Neurol. 2009. PMID: 19225139 Free PMC article. Clinical Trial.
67 results