Speer MC - Search Results

1

Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients.

Milhorat TH, Chou MW, Trinidad EM, Kula RW, Mandell M, Wolpert C, Speer MC. Milhorat TH, et al. Among authors: speer mc. Neurosurgery. 1999 May;44(5):1005-17. doi: 10.1097/00006123-199905000-00042. Neurosurgery. 1999. PMID: 10232534

2

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, Oro' JJ, Iskandar BJ, George TM, Milhorat TH, Speer MC. Boyles AL, et al. Among authors: speer mc. Am J Med Genet A. 2006 Dec 15;140(24):2776-85. doi: 10.1002/ajmg.a.31546. Am J Med Genet A. 2006. PMID: 17103432

3

Clinical, radiological, and genetic similarities between patients with Chiari Type I and Type 0 malformations.

Markunas CA, Tubbs RS, Moftakhar R, Ashley-Koch AE, Gregory SG, Oakes WJ, Speer MC, Iskandar BJ. Markunas CA, et al. Among authors: speer mc. J Neurosurg Pediatr. 2012 Apr;9(4):372-8. doi: 10.3171/2011.12.PEDS11113. J Neurosurg Pediatr. 2012. PMID: 22462700 Free PMC article.

4

A genetic hypothesis for Chiari I malformation with or without syringomyelia.

Speer MC, George TM, Enterline DS, Franklin A, Wolpert CM, Milhorat TH. Speer MC, et al. Neurosurg Focus. 2000 Mar 15;8(3):E12. doi: 10.3171/foc.2000.8.3.12. Neurosurg Focus. 2000. PMID: 16676924

5

Genetic studies in neural tube defects. NTD Collaborative Group.

Melvin EC, George TM, Worley G, Franklin A, Mackey J, Viles K, Shah N, Drake CR, Enterline DS, McLone D, Nye J, Oakes WJ, McLaughlin C, Walker ML, Peterson P, Brei T, Buran C, Aben J, Ohm B, Bermans I, Qumsiyeh M, Vance J, Pericak-Vance MA, Speer MC. Melvin EC, et al. Among authors: speer mc. Pediatr Neurosurg. 2000 Jan;32(1):1-9. doi: 10.1159/000028889. Pediatr Neurosurg. 2000. PMID: 10765131 Review.

6

The brain-derived neurotrophic factor VAL66MET polymorphism and cerebral white matter hyperintensities in late-life depression.

Taylor WD, Züchner S, McQuoid DR, Payne ME, MacFall JR, Steffens DC, Speer MC, Krishnan KR. Taylor WD, et al. Among authors: speer mc. Am J Geriatr Psychiatry. 2008 Apr;16(4):263-71. doi: 10.1097/JGP.0b013e3181591c30. Epub 2008 Feb 8. Am J Geriatr Psychiatry. 2008. PMID: 18263664

7

Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia.

Stamm DS, Aylsworth AS, Stajich JM, Kahler SG, Thorne LB, Speer MC, Powell CM. Stamm DS, et al. Among authors: speer mc. Am J Med Genet A. 2008 Jul 15;146A(14):1832-41. doi: 10.1002/ajmg.a.32370. Am J Med Genet A. 2008. PMID: 18553514

8

Use of LINKAGE programs for linkage analysis.

Speer MC. Speer MC. Curr Protoc Hum Genet. 2006 Feb;Chapter 1:Unit 1.7. doi: 10.1002/0471142905.hg0107s48. Curr Protoc Hum Genet. 2006. PMID: 18428385 Review.

9

Harnessing the power of the pedigree.

Wolpert CM, Speer MC. Wolpert CM, et al. Among authors: speer mc. J Midwifery Womens Health. 2005 May-Jun;50(3):189-96. doi: 10.1016/j.jmwh.2005.02.003. J Midwifery Womens Health. 2005. PMID: 15894996 Review.

10

Review Article: Chiari Type I Malformation with or Without Syringomyelia: Prevalence and Genetics.

Speer MC, Enterline DS, Mehltretter L, Hammock P, Joseph J, Dickerson M, Ellenbogen RG, Milhorat TH, Hauser MA, George TM. Speer MC, et al. J Genet Couns. 2003 Aug;12(4):297-311. doi: 10.1023/A:1023948921381. J Genet Couns. 2003. PMID: 26141174

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