Stevenson DA - Search Results

1

Hyperactive Ras/MAPK signaling is critical for tibial nonunion fracture in neurofibromin-deficient mice.

Sharma R, Wu X, Rhodes SD, Chen S, He Y, Yuan J, Li J, Yang X, Li X, Jiang L, Kim ET, Stevenson DA, Viskochil D, Xu M, Yang FC. Sharma R, et al. Among authors: stevenson da. Hum Mol Genet. 2013 Dec 1;22(23):4818-28. doi: 10.1093/hmg/ddt333. Epub 2013 Jul 17. Hum Mol Genet. 2013. PMID: 23863460 Free PMC article.

2

Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1.

Stevenson DA, Birch PH, Friedman JM, Viskochil DH, Balestrazzi P, Boni S, Buske A, Korf BR, Niimura M, Pivnick EK, Schorry EK, Short MP, Tenconi R, Tonsgard JH, Carey JC. Stevenson DA, et al. Am J Med Genet. 1999 Jun 11;84(5):413-9. doi: 10.1002/(sici)1096-8628(19990611)84:5<413::aid-ajmg5>3.0.co;2-1. Am J Med Genet. 1999. PMID: 10360395

3

Case-control study of the muscular compartments and osseous strength in neurofibromatosis type 1 using peripheral quantitative computed tomography.

Stevenson DA, Moyer-Mileur LJ, Carey JC, Quick JL, Hoff CJ, Viskochil DH. Stevenson DA, et al. J Musculoskelet Neuronal Interact. 2005 Jun;5(2):145-9. J Musculoskelet Neuronal Interact. 2005. PMID: 15951630 Free article.

4

Clinical and molecular aspects of an informative family with neurofibromatosis type 1 and Noonan phenotype.

Stevenson DA, Viskochil DH, Rope AF, Carey JC. Stevenson DA, et al. Clin Genet. 2006 Mar;69(3):246-53. doi: 10.1111/j.1399-0004.2006.00576.x. Clin Genet. 2006. PMID: 16542390 Free PMC article.

5

Double inactivation of NF1 in tibial pseudarthrosis.

Stevenson DA, Zhou H, Ashrafi S, Messiaen LM, Carey JC, D'Astous JL, Santora SD, Viskochil DH. Stevenson DA, et al. Am J Hum Genet. 2006 Jul;79(1):143-8. doi: 10.1086/504441. Epub 2006 May 10. Am J Hum Genet. 2006. PMID: 16773574 Free PMC article.

6

Bone mineral density in children and adolescents with neurofibromatosis type 1.

Stevenson DA, Moyer-Mileur LJ, Murray M, Slater H, Sheng X, Carey JC, Dube B, Viskochil DH. Stevenson DA, et al. J Pediatr. 2007 Jan;150(1):83-8. doi: 10.1016/j.jpeds.2006.10.048. J Pediatr. 2007. PMID: 17188620 Free PMC article.

7

The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1.

Stevenson DA, Viskochil DH, Schorry EK, Crawford AH, D'Astous J, Murray KA, Friedman JM, Armstrong L, Carey JC. Stevenson DA, et al. Genet Med. 2007 Jul;9(7):409-12. doi: 10.1097/gim.0b013e3180986e05. Genet Med. 2007. PMID: 17666887 Free PMC article. Review.

8

Neurofibromatosis type 1 is a genetic skeletal disorder.

Stevenson DA, Viskochil DH, Carey JC. Stevenson DA, et al. Am J Med Genet A. 2007 Sep 1;143A(17):2082-3; author reply 2084. doi: 10.1002/ajmg.a.31758. Am J Med Genet A. 2007. PMID: 17702004 No abstract available.

9

Evidence of increased bone resorption in neurofibromatosis type 1 using urinary pyridinium crosslink analysis.

Stevenson DA, Schwarz EL, Viskochil DH, Moyer-Mileur LJ, Murray M, Firth SD, D'Astous JL, Carey JC, Pasquali M. Stevenson DA, et al. Pediatr Res. 2008 Jun;63(6):697-701. doi: 10.1203/PDR.0b013e31816fee45. Pediatr Res. 2008. PMID: 18317233 Free PMC article.

10

Bone mineral density in children with neurofibromatosis type 1.

Stevenson DA, Murray M, Viskochil DH, Carey JC, Moyer-Mileur LJ. Stevenson DA, et al. J Pediatr Orthop. 2008 Oct-Nov;28(7):791; author reply 791-2. doi: 10.1097/BPO.0b013e3181857ebe. J Pediatr Orthop. 2008. PMID: 18812910 No abstract available.

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