Chiari Type 1 Malformation/Syringomyelia Publications

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Publications

Chiari Type 1 Malformation/Syringomyelia

Speer MC, Enterline DS, Mehltretter L, Hammock P, Joseph J, Dickerson M, Ellenbogen RG, Milhorat TH, Hauser MA, George TM. Chiari Type I Malformation With or Without Syringomyelia: Prevalence and Genetics. Journal of Genetic Counseling 12(4):297, 2003.

Speer MC, George TM, Enterline DS, Franklin A, Wolpert CM, Milhorat TH. A Genetic Hypothesis for Chiari Type 1 Malformation with or without Syringomyelia (CM1/S). Neurosurgical Focus 8(3):12, March 2000.

Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert CM, Speer MC. Chiari I Malformation Redefined: Clinical, Radiographic and Genetic Features in 364 Symptomatic Patients. Journal of Neurosurgery 44:1005-1017, 1999.

Wolpert CM, Milhorat TH, Trinidad EM, Franklin AD, George TM, Enterline DS, Speer MC. Further Evidence for Familial Aggregation for Chiari type 1 malformation. American Society of Human Genetics 63: A124, 696, 1998.

Wolpert CM, Speer MC, Trinidad EM, Mu H, Gripps KW, Econs MJ, Alysworth AS, Milhorat TH. Association of Chiari Type 1 Malformation and Primary Empty Sella Turcica: Two Case Reports With Retrospective Data Review. American Society of Human Genetics 61: A116, 657, 1997.

Wolpert CM, Gripps KW, Mu H, Trinidad EM, Milhorat TH, Speer MC. Familial Aggregation of Chiari Type 1 Malformations in 8 Families. American Society of Human Genetics 59: A109, 599, 1996.

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