Porter DE - Search Results

1

Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study.

Porter DE, Lonie L, Fraser M, Dobson-Stone C, Porter JR, Monaco AP, Simpson AH. Porter DE, et al. Among authors: porter jr. J Bone Joint Surg Br. 2004 Sep;86(7):1041-6. doi: 10.1302/0301-620x.86b7.14815. J Bone Joint Surg Br. 2004. PMID: 15446535

2

Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases.

Lonie L, Porter DE, Fraser M, Cole T, Wise C, Yates L, Wakeling E, Blair E, Morava E, Monaco AP, Ragoussis J. Lonie L, et al. Among authors: porter de. Hum Mutat. 2006 Nov;27(11):1160. doi: 10.1002/humu.9467. Hum Mutat. 2006. PMID: 17041877

3

Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses.

Philippe C, Porter DE, Emerton ME, Wells DE, Simpson AH, Monaco AP. Philippe C, et al. Among authors: porter de. Am J Hum Genet. 1997 Sep;61(3):520-8. doi: 10.1086/515505. Am J Hum Genet. 1997. PMID: 9326317 Free PMC article.

4

The neoplastic pathogenesis of solitary and multiple osteochondromas.

Porter DE, Simpson AH. Porter DE, et al. J Pathol. 1999 Jun;188(2):119-25. doi: 10.1002/(SICI)1096-9896(199906)188:2<119::AID-PATH321>3.0.CO;2-N. J Pathol. 1999. PMID: 10398153 Review.

5

Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses.

Dobson-Stone C, Cox RD, Lonie L, Southam L, Fraser M, Wise C, Bernier F, Hodgson S, Porter DE, Simpson AH, Monaco AP. Dobson-Stone C, et al. Among authors: porter de. Eur J Hum Genet. 2000 Jan;8(1):24-32. doi: 10.1038/sj.ejhg.5200409. Eur J Hum Genet. 2000. PMID: 10713884

6

Clinical and radiographic analysis of osteochondromas and growth disturbance in hereditary multiple exostoses.

Porter DE, Emerton ME, Villanueva-Lopez F, Simpson AH. Porter DE, et al. J Pediatr Orthop. 2000 Mar-Apr;20(2):246-50. J Pediatr Orthop. 2000. PMID: 10739291

7

The association between ulnar length and forearm movement in patients with multiple osteochondromas.

Watts AC, Ballantyne JA, Fraser M, Simpson AH, Porter DE. Watts AC, et al. Among authors: porter de. J Hand Surg Am. 2007 May-Jun;32(5):667-73. doi: 10.1016/j.jhsa.2007.02.008. J Hand Surg Am. 2007. PMID: 17482006

8

Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostoses.

Park KJ, Shin KH, Ku JL, Cho TJ, Lee SH, Choi IH, Phillipe C, Monaco AP, Porter DE, Park JG. Park KJ, et al. Among authors: porter de. J Hum Genet. 1999;44(4):230-4. doi: 10.1007/s100380050149. J Hum Genet. 1999. PMID: 10429361

9

Forearm deformity in patients with hereditary multiple exostoses: factors associated with range of motion and radial head dislocation.

Clement ND, Porter DE. Clement ND, et al. Among authors: porter de. J Bone Joint Surg Am. 2013 Sep 4;95(17):1586-92. doi: 10.2106/JBJS.L.00736. J Bone Joint Surg Am. 2013. PMID: 24005199

10

The hip in hereditary multiple exostoses.

Porter DE, Benson MK, Hosney GA. Porter DE, et al. J Bone Joint Surg Br. 2001 Sep;83(7):988-95. doi: 10.1302/0301-620x.83b7.10779. J Bone Joint Surg Br. 2001. PMID: 11603538

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