Proud V - Search Results

1

Neonatal upper airway obstruction in osteogenesis imperfecta: series of three cases and review of the literature.

Johnson K, Pineda M, Darrow D, Proud V, Derkay C. Johnson K, et al. Among authors: proud v. Ann Otol Rhinol Laryngol. 2008 Jan;117(1):27-31. doi: 10.1177/000348940811700107. Ann Otol Rhinol Laryngol. 2008. PMID: 18254368

2

Role of the pediatric otolaryngologist in diagnosis and management of children with mucopolysaccharidoses.

Wold SM, Derkay CS, Darrow DH, Proud V. Wold SM, et al. Among authors: proud v. Int J Pediatr Otorhinolaryngol. 2010 Jan;74(1):27-31. doi: 10.1016/j.ijporl.2009.09.042. Epub 2009 Nov 20. Int J Pediatr Otorhinolaryngol. 2010. PMID: 19931921

3

Classification of the dysmorphology of pectus excavatum.

Cartoski MJ, Nuss D, Goretsky MJ, Proud VK, Croitoru DP, Gustin T, Mitchell K, Vasser E, Kelly RE Jr. Cartoski MJ, et al. J Pediatr Surg. 2006 Sep;41(9):1573-81. doi: 10.1016/j.jpedsurg.2006.05.055. J Pediatr Surg. 2006. PMID: 16952594

4

Advancing our understanding of the inheritance and transmission of pectus excavatum.

Horth L, Stacey MW, Proud VK, Segna K, Rutherford C, Nuss D, Kelly RE. Horth L, et al. Among authors: proud vk. J Pediatr Genet. 2012 Sep;1(3):161-73. doi: 10.3233/PGE-2012-026. J Pediatr Genet. 2012. PMID: 27625818 Free PMC article.

5

Unique family with Townes-Brocks syndrome, SALL1 mutation, and cardiac defects.

Surka WS, Kohlhase J, Neunert CE, Schneider DS, Proud VK. Surka WS, et al. Among authors: proud vk. Am J Med Genet. 2001 Aug 15;102(3):250-7. doi: 10.1002/1096-8628(20010815)102:3<250::aid-ajmg1479>3.0.co;2-q. Am J Med Genet. 2001. PMID: 11484202

6

Family study of the inheritance of pectus excavatum.

Creswick HA, Stacey MW, Kelly RE Jr, Gustin T, Nuss D, Harvey H, Goretsky MJ, Vasser E, Welch JC, Mitchell K, Proud VK. Creswick HA, et al. J Pediatr Surg. 2006 Oct;41(10):1699-703. doi: 10.1016/j.jpedsurg.2006.05.071. J Pediatr Surg. 2006. PMID: 17011272

7

Variable number of tandem repeat polymorphisms (VNTRs) in the ACAN gene associated with pectus excavatum.

Stacey MW, Neumann SA, Dooley A, Segna K, Kelly RE, Nuss D, Kuhn AM, Goretsky MJ, Fecteau AH, Pastor A, Proud VK. Stacey MW, et al. Among authors: proud vk. Clin Genet. 2010 Nov;78(5):502-4. doi: 10.1111/j.1399-0004.2010.01492.x. Clin Genet. 2010. PMID: 21039430 No abstract available.

8

Pacman dysplasia: a lethal skeletal dysplasia with variable radiographic features.

Miller SF, Proud VK, Werner AL, Field FM, Wilcox WF, Lachman RS, Rimoin DL. Miller SF, et al. Pediatr Radiol. 2003 Apr;33(4):256-60. doi: 10.1007/s00247-002-0859-4. Epub 2003 Feb 5. Pediatr Radiol. 2003. PMID: 12709756

9

Weaver syndrome: autosomal dominant inheritance of the disorder.

Proud VK, Braddock SR, Cook L, Weaver DD. Proud VK, et al. Am J Med Genet. 1998 Oct 2;79(4):305-10. doi: 10.1002/(sici)1096-8628(19981002)79:4<305::aid-ajmg13>3.0.co;2-v. Am J Med Genet. 1998. PMID: 9781912

10

CNS malformation in a child with Kabuki (Niikawa-Kuroki) syndrome: report and review.

Chu DC, Finley SC, Young DW, Proud VK. Chu DC, et al. Among authors: proud vk. Am J Med Genet. 1997 Oct 17;72(2):205-9. Am J Med Genet. 1997. PMID: 9382144

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