Direttore Dipartimento di Medicina Pediatrica e Neurolologia Texas Children's Hospital
USA
Specializzazione in Neurologia Pediatrica.
Gli interessi di ricerca del Dr. Glaze si concentrano sulla Sindrome di Rett e includono uno studio di storia naturale, comprese correlazioni genotipo / fenotipo, qualità della vita, e la sopravvivenza. I suoi studi sono focalizzati sulla caratterizzazione del comportamento del sonno nei bambini con malattie neurologiche rare.
PUBBLICAZIONI SELEZIONATE:
Glaze DG, Percy AK, Skinner S, Motil KJ, Neul JL, Barrish JO, Lane JB, Geerts SP, Annese F, Graham J, McNair L, Lee HS. Epilepsy and the natural history of Rett syndrome. Neurology 2010; 74(11):909-12.
Kirby RS, Lane JB, Childers J, Skinner SA, Annese F, Barrish JO, Glaze DG, Macleod P, Percy AK. Longevity in Rett syndrome: analysis of the North American Database. Journal of Pediatrics 2010; 156(1):135-138.e1.
Ramocki MB, Peters SU, Tavyev YJ, Zhang F, Carvalho CM, Schaaf CP, Richman R, Fang P, Glaze DG, Lupski JR, Zoghbi HY. Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome. Annals of Neurology 2009; 66(6):771-82. (PubMed).
Percy AK, Lee HS, Neul JL, Lane JB, Skinner SA, Geerts SP, Annese F, Graham J, McNair L, Motil KJ, Barrish JO, Glaze DG. Profiling scoliosis in Rett syndrome. Pediatric Research 2009. (PubMed).
Samaco RC, Mandel-Brehm C, Chao HT, Ward CS, Fyffe-Maricich SL, Ren J, Hyland K, Thaller C, Maricich SM, Humphreys P, Greer JJ, Percy A, Glaze DG, Zoghbi HY, Neul JL. Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities. Proceedings of the National Academy of Sciences of the United States of America 2009;106(51):21966-71. (PubMed).