Gurnett CA - Search Results

1

Genome-wide association study identifies new disease loci for isolated clubfoot.

Zhang TX, Haller G, Lin P, Alvarado DM, Hecht JT, Blanton SH, Stephens Richards B, Rice JP, Dobbs MB, Gurnett CA. Zhang TX, et al. Among authors: gurnett ca. J Med Genet. 2014 May;51(5):334-9. doi: 10.1136/jmedgenet-2014-102303. Epub 2014 Mar 25. J Med Genet. 2014. PMID: 24667120

2

Treatment of idiopathic clubfoot: an historical review.

Dobbs MB, Morcuende JA, Gurnett CA, Ponseti IV. Dobbs MB, et al. Among authors: gurnett ca. Iowa Orthop J. 2000;20:59-64. Iowa Orthop J. 2000. PMID: 10934626 Free PMC article.

3

Factors predictive of outcome after use of the Ponseti method for the treatment of idiopathic clubfeet.

Dobbs MB, Rudzki JR, Purcell DB, Walton T, Porter KR, Gurnett CA. Dobbs MB, et al. Among authors: gurnett ca. J Bone Joint Surg Am. 2004 Jan;86(1):22-7. doi: 10.2106/00004623-200401000-00005. J Bone Joint Surg Am. 2004. PMID: 14711941 Free article.

4

Flexor digitorum accessorius longus muscle is associated with familial idiopathic clubfoot.

Dobbs MB, Walton T, Gordon JE, Schoenecker PL, Gurnett CA. Dobbs MB, et al. Among authors: gurnett ca. J Pediatr Orthop. 2005 May-Jun;25(3):357-9. doi: 10.1097/01.bpo.0000152908.08422.95. J Pediatr Orthop. 2005. PMID: 15832155

5

Variable hand and foot abnormalities in family with congenital vertical talus and CDMP-1 gene mutation.

Dobbs MB, Gurnett CA, Robarge J, Gordon JE, Morcuende JA, Bowcock AM. Dobbs MB, et al. Among authors: gurnett ca. J Orthop Res. 2005 Nov;23(6):1490-4. doi: 10.1016/j.orthres.2005.04.011.1100230636. Epub 2005 Jul 11. J Orthop Res. 2005. PMID: 16005596 Free article.

6

HOXD10 M319K mutation in a family with isolated congenital vertical talus.

Dobbs MB, Gurnett CA, Pierce B, Exner GU, Robarge J, Morcuende JA, Cole WG, Templeton PA, Foster B, Bowcock AM. Dobbs MB, et al. Among authors: gurnett ca. J Orthop Res. 2006 Mar;24(3):448-53. doi: 10.1002/jor.20052. J Orthop Res. 2006. PMID: 16450407 Free article.

7

Evidence for an additional locus for split hand/foot malformation in chromosome region 8q21.11-q22.3.

Gurnett CA, Dobbs MB, Nordsieck EJ, Keppel C, Goldfarb CA, Morcuende JA, Bowcock AM. Gurnett CA, et al. Am J Med Genet A. 2006 Aug 15;140(16):1744-8. doi: 10.1002/ajmg.a.31375. Am J Med Genet A. 2006. PMID: 16838310

8

Additional evidence of a locus for complex febrile and afebrile seizures on chromosome 12q22-23.3.

Gurnett CA, Dobbs MB, Keppel CR, Pincus ER, Jansen LA, Bowcock AM. Gurnett CA, et al. Neurogenetics. 2007 Jan;8(1):61-3. doi: 10.1007/s10048-006-0063-z. Epub 2006 Sep 14. Neurogenetics. 2007. PMID: 16972079 No abstract available.

9

Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly.

Gurnett CA, Bowcock AM, Dietz FR, Morcuende JA, Murray JC, Dobbs MB. Gurnett CA, et al. Am J Med Genet A. 2007 Jan 1;143A(1):27-32. doi: 10.1002/ajmg.a.31563. Am J Med Genet A. 2007. PMID: 17152067

10

Absence of HOXD10 mutations in idiopathic clubfoot and sporadic vertical talus.

Gurnett CA, Keppel C, Bick J, Bowcock AM, Dobbs MB. Gurnett CA, et al. Clin Orthop Relat Res. 2007 Sep;462:27-31. doi: 10.1097/BLO.0b013e31805d8649. Clin Orthop Relat Res. 2007. PMID: 17417092

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