Below is a list of publications that resulted from ASAP funded research. Click on title for more information.
Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15.
Boyles AL, Enterline DS, Hammock PH, Siegel DG, Slifer SH, Mehltretter L, Gilbert JR, Hu-Lince D, Stephan D, Batzdorf U, Benzel E, Ellenbogen R, Green BA, Kula R, Menezes A, Mueller D, OrÃ³ JJ, Iskandar BJ, George TM, Milhorat TH, Speer MC.
Asymptomatic Chiari Type I malformations identified on magnetic resonance imaging.
Meadows J, Kraut M, Guarnieri M, Haroun RI, Carson BS
A genetic hypothesis for Chiari I malformation with or without syringomyelia.
Marcy C. Speer, Timothy M. George, David S. Enterline, Amy Franklin, Chantelle M. Wolpert, and Thomas H. Milhorat
Syringomyelia hydrodynamics: an in vitro study based on in vivo measurements.
Martin BA, Kalata W, Loth F, Royston TJ, Oshinski JN