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Guidelines for reporting clinical features in cases with MECP2 mutations.
Kerr AM, Nomura Y, Armstrong D, Anvret M, Belichenko PV, Budden S, Cass H, Christodoulou J, Clarke A, Ellaway C, d'Esposito M, Francke U, Hulten M, Julu P, Leonard H, Naidu S, Schanen C, Webb T, Engerstrom IW, Yamashita Y, Segawa M. Kerr AM, et al. Among authors: naidu s. Brain Dev. 2001 Jul;23(4):208-11. doi: 10.1016/s0387-7604(01)00193-0. Brain Dev. 2001. PMID: 11376997
MeCP2 mutations in children with and without the phenotype of Rett syndrome.
Hoffbuhr K, Devaney JM, LaFleur B, Sirianni N, Scacheri C, Giron J, Schuette J, Innis J, Marino M, Philippart M, Narayanan V, Umansky R, Kronn D, Hoffman EP, Naidu S. Hoffbuhr K, et al. Among authors: naidu s. Neurology. 2001 Jun 12;56(11):1486-95. doi: 10.1212/wnl.56.11.1486. Neurology. 2001. PMID: 11402105
Functional outcomes in Rett syndrome.
Pidcock FS, Salorio C, Bibat G, Swain J, Scheller J, Shore W, Naidu S. Pidcock FS, et al. Among authors: naidu s. Brain Dev. 2016 Jan;38(1):76-81. doi: 10.1016/j.braindev.2015.06.005. Epub 2015 Jul 11. Brain Dev. 2016. PMID: 26175308 Free PMC article.
839 results