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Page 1
MeCP2 dysfunction in humans and mice.
Zoghbi HY. Zoghbi HY. J Child Neurol. 2005 Sep;20(9):736-40. doi: 10.1177/08830738050200090701. J Child Neurol. 2005. PMID: 16225828 Review.
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. J Child Neurol. 2007 Dec;22(12):1338-41. doi: 10.1177/0883073807308715. J Child Neurol. 2007. PMID: 18174548
Rett syndrome: recent research progress.
Percy AK. Percy AK. J Child Neurol. 2008 May;23(5):543-9. doi: 10.1177/0883073807309786. Epub 2007 Dec 3. J Child Neurol. 2008. PMID: 18056689 Review.
Rett syndrome: clinical and molecular update.
Percy AK, Lane JB. Percy AK, et al. Curr Opin Pediatr. 2004 Dec;16(6):670-7. doi: 10.1097/01.mop.0000143693.59408.ce. Curr Opin Pediatr. 2004. PMID: 15548931 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
25 results