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Evaluation of QTc in Rett syndrome: Correlation with age, severity, and genotype.
Crosson J, Srivastava S, Bibat GM, Gupta S, Kantipuly A, Smith-Hicks C, Myers SM, Sanyal A, Yenokyan G, Brenner J, Naidu SR. Crosson J, et al. Among authors: naidu sr. Am J Med Genet A. 2017 Jun;173(6):1495-1501. doi: 10.1002/ajmg.a.38191. Epub 2017 Apr 10. Am J Med Genet A. 2017. PMID: 28394409 Free PMC article.
Functional outcomes in Rett syndrome.
Pidcock FS, Salorio C, Bibat G, Swain J, Scheller J, Shore W, Naidu S. Pidcock FS, et al. 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.
Monogenic disorders that mimic the phenotype of Rett syndrome.
Srivastava S, Desai S, Cohen J, Smith-Hicks C, Barañano K, Fatemi A, Naidu S. Srivastava S, et al. Neurogenetics. 2018 Jan;19(1):41-47. doi: 10.1007/s10048-017-0535-3. Epub 2018 Jan 10. Neurogenetics. 2018. PMID: 29322350 Free PMC article.
Clinical variability in Rett syndrome.
Naidu S, Bibat G, Kratz L, Kelley RI, Pevsner J, Hoffman E, Cuffari C, Rohde C, Blue ME, Johnston MV. Naidu S, et al. J Child Neurol. 2003 Oct;18(10):662-8. doi: 10.1177/08830738030180100801. J Child Neurol. 2003. PMID: 14649546 Review.
BRAT1 mutations present with a spectrum of clinical severity.
Srivastava S, Olson HE, Cohen JS, Gubbels CS, Lincoln S, Davis BT, Shahmirzadi L, Gupta S, Picker J, Yu TW, Miller DT, Soul JS, Poretti A, Naidu S. Srivastava S, et al. Am J Med Genet A. 2016 Sep;170(9):2265-73. doi: 10.1002/ajmg.a.37783. Epub 2016 Jun 9. Am J Med Genet A. 2016. PMID: 27282546 Free PMC article. Review.
196 results