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Oxidative stress in Rett syndrome.
Sierra C, Vilaseca MA, Brandi N, Artuch R, Mira A, Nieto M, Pineda M. Sierra C, et al. Among authors: pineda m. Brain Dev. 2001 Dec;23 Suppl 1:S236-9. doi: 10.1016/s0387-7604(01)00369-2. Brain Dev. 2001. PMID: 11738881
Prenatal diagnosis in Rett syndrome.
Armstrong J, Aibar E, Pineda M, Pérez MM, Geán E, Carrera M, Casas C, Martínez F, Monrós E. Armstrong J, et al. Among authors: pineda m. Fetal Diagn Ther. 2002 Jul-Aug;17(4):200-4. doi: 10.1159/000059370. Fetal Diagn Ther. 2002. PMID: 12065946
Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.
Mencarelli MA, Spanhol-Rosseto A, Artuso R, Rondinella D, De Filippis R, Bahi-Buisson N, Nectoux J, Rubinsztajn R, Bienvenu T, Moncla A, Chabrol B, Villard L, Krumina Z, Armstrong J, Roche A, Pineda M, Gak E, Mari F, Ariani F, Renieri A. Mencarelli MA, et al. Among authors: pineda m. J Med Genet. 2010 Jan;47(1):49-53. doi: 10.1136/jmg.2009.067884. Epub 2009 Jul 2. J Med Genet. 2010. PMID: 19578037
Cognitive stimulation has potential for brain activation in individuals with Rett syndrome.
Migliorelli C, Medina-Rivera I, Bachiller A, Tost A, Alonso JF, López-Sala A, Armstrong J, O'Callahan MDM, Pineda M, Mañanas MA, Romero S, García-Cazorla Á. Migliorelli C, et al. Among authors: pineda m. J Intellect Disabil Res. 2022 Mar;66(3):213-224. doi: 10.1111/jir.12902. Epub 2021 Nov 18. J Intellect Disabil Res. 2022. PMID: 34796573
Mutations in JMJD1C are involved in Rett syndrome and intellectual disability.
Sáez MA, Fernández-Rodríguez J, Moutinho C, Sanchez-Mut JV, Gomez A, Vidal E, Petazzi P, Szczesna K, Lopez-Serra P, Lucariello M, Lorden P, Delgado-Morales R, de la Caridad OJ, Huertas D, Gelpí JL, Orozco M, López-Doriga A, Milà M, Perez-Jurado LA, Pineda M, Armstrong J, Lázaro C, Esteller M. Sáez MA, et al. Among authors: pineda m. Genet Med. 2016 Apr;18(4):378-85. doi: 10.1038/gim.2015.100. Epub 2015 Jul 16. Genet Med. 2016. PMID: 26181491 Free PMC article.
742 results