The goal of this Rett Center Core is: 1) to coordinate and unite the individual Projects into an integrated Research Program Project, 2) to facilitate the successful completion of the specific aims of the proposed projects, and 3) to initiate the design and development of future projects. The Core will ensure the integration of the Research Program Project as a whole by promoting dynamic interactions among individual investigators and with other scientists, particularly our External Advisors. These interactions will promote and ensure the growth of the Research Program Project by sharing information, critiquing current research efforts, and formulating new hypotheses and research designs. The research efforts of this Program Project will be closely monitored by members of the Core that include Drs. Glaze, Armstrong, Dunn, and Ms. Schultz, most of whom have been involved in this Research Program Project since its inception, and ensure the continuity of our research efforts. The Core is the center for patient identification, education, follow-up and research protocol enrollment. Members of the Core will provide longitudinal assessment of a large, well defined and established group of RS individuals, thereby providing clinical profiles to correlate with the research efforts of the individual projects. Under the direction of Dr. J.K. Dunn, the Core provides statistical design and analysis support and continues to develop an already extensive data base that is used regularly not only for patient identification and selection, but also for the generation of hypotheses. These activities of the Core ensure integration of the Research Program Project as a whole by bringing together our multidisciplinary team to study in an integrated the many dimensions of RS.

Project Start
Project End
Budget Start
Budget End
Support Year
9
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Baylor College of Medicine
Department
Type
DUNS #
074615394
City
Houston
State
TX
Country
United States
Zip Code
77030
Motil, Kathleen J; Schultz, Rebecca J; Abrams, Steven et al. (2006) Fractional calcium absorption is increased in girls with Rett syndrome. J Pediatr Gastroenterol Nutr 42:419-26
Armstrong, D D; Assmann, S; Kinney, H C (1999) Early developmental changes in the chemoarchitecture of the human inferior olive: a review. J Neuropathol Exp Neurol 58:1-11
Motil, K J; Schultz, R J; Browning, K et al. (1999) Oropharyngeal dysfunction and gastroesophageal dysmotility are present in girls and women with Rett syndrome. J Pediatr Gastroenterol Nutr 29:31-7
Glaze, D G; Schultz, R J; Frost, J D (1998) Rett syndrome: characterization of seizures versus non-seizures. Electroencephalogr Clin Neurophysiol 106:79-83
Armstrong, D D; Dunn, K; Antalffy, B (1998) Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with trisomy 21. J Neuropathol Exp Neurol 57:1013-7
Schultz, R; Glaze, D; Motil, K et al. (1998) Hand and foot growth failure in Rett syndrome. J Child Neurol 13:71-4
Wan, M; Cravatt, B F; Ring, H Z et al. (1998) Conserved chromosomal location and genomic structure of human and mouse fatty-acid amide hydrolase genes and evaluation of clasper as a candidate neurological mutation. Genomics 54:408-14
Cummings, C J; Dahle, E J; Zoghbi, H Y (1998) Analysis of the genomic structure of the human glycine receptor alpha2 subunit gene and exclusion of this gene as a candidate for Rett syndrome. Am J Med Genet 78:176-8
Van den Veyver, I B; Subramanian, S; Zoghbi, H Y (1998) Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome. Am J Med Genet 78:179-81
Motil, K J; Schultz, R J; Wong, W W et al. (1998) Increased energy expenditure associated with repetitive involuntary movement does not contribute to growth failure in girls with Rett syndrome. J Pediatr 132:228-33

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