McElhinney DB - Search Results

1

Evaluating the role of connexin43 in congenital heart disease: Screening for mutations in patients with outflow tract anomalies and the analysis of knock-in mouse models.

Huang GY, Xie LJ, Linask KL, Zhang C, Zhao XQ, Yang Y, Zhou GM, Wu YJ, Marquez-Rosado L, McElhinney DB, Goldmuntz E, Liu C, Lampe PD, Chatterjee B, Lo CW. Huang GY, et al. Among authors: mcelhinney db. J Cardiovasc Dis Res. 2011 Oct;2(4):206-12. doi: 10.4103/0975-3583.89804. J Cardiovasc Dis Res. 2011. PMID: 22135478 Free PMC article.

2

Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching.

McElhinney DB, Clark BJ 3rd, Weinberg PM, Kenton ML, McDonald-McGinn D, Driscoll DA, Zackai EH, Goldmuntz E. McElhinney DB, et al. J Am Coll Cardiol. 2001 Jun 15;37(8):2114-9. doi: 10.1016/s0735-1097(01)01286-4. J Am Coll Cardiol. 2001. PMID: 11419896 Free article.

3

Patterns of right aortic arch and mirror-image branching of the brachiocephalic vessels without associated anomalies.

McElhinney DB, Hoydu AK, Gaynor JW, Spray TL, Goldmuntz E, Weinberg PM. McElhinney DB, et al. Pediatr Cardiol. 2001 Jul-Aug;22(4):285-91. doi: 10.1007/s002460010231. Pediatr Cardiol. 2001. PMID: 11455394

4

Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of age.

McElhinney DB, McDonald-McGinn D, Zackai EH, Goldmuntz E. McElhinney DB, et al. Pediatrics. 2001 Dec;108(6):E104. doi: 10.1542/peds.108.6.e104. Pediatrics. 2001. PMID: 11731631

5

Chromosomal and cardiovascular anomalies associated with congenital laryngeal web.

McElhinney DB, Jacobs I, McDonald-McGinn DM, Zackai EH, Goldmuntz E. McElhinney DB, et al. Int J Pediatr Otorhinolaryngol. 2002 Oct 21;66(1):23-27. doi: 10.1016/s0165-5876(02)00184-2. Int J Pediatr Otorhinolaryngol. 2002. PMID: 12363418

6

Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome.

McElhinney DB, Krantz ID, Bason L, Piccoli DA, Emerick KM, Spinner NB, Goldmuntz E. McElhinney DB, et al. Circulation. 2002 Nov 12;106(20):2567-74. doi: 10.1161/01.cir.0000037221.45902.69. Circulation. 2002. PMID: 12427653

7

Correlation between abnormal cardiac physical examination and echocardiographic findings in neonates with Down syndrome.

McElhinney DB, Straka M, Goldmuntz E, Zackai EH. McElhinney DB, et al. Am J Med Genet. 2002 Dec 1;113(3):238-41. doi: 10.1002/ajmg.10803. Am J Med Genet. 2002. PMID: 12439890

8

Association between cardiac tumors and tuberous sclerosis in the fetus and neonate.

Tworetzky W, McElhinney DB, Margossian R, Moon-Grady AJ, Sallee D, Goldmuntz E, van der Velde ME, Silverman NH, Allan LD. Tworetzky W, et al. Among authors: mcelhinney db. Am J Cardiol. 2003 Aug 15;92(4):487-9. doi: 10.1016/s0002-9149(03)00677-5. Am J Cardiol. 2003. PMID: 12914889

9

Chromosome 22q11 deletion in patients with truncus arteriosus.

McElhinney DB, Driscoll DA, Emanuel BS, Goldmuntz E. McElhinney DB, et al. Pediatr Cardiol. 2003 Nov-Dec;24(6):569-73. doi: 10.1007/s00246-003-0441-3. Epub 2003 Sep 4. Pediatr Cardiol. 2003. PMID: 12947506

10

NKX2.5 mutations in patients with congenital heart disease.

McElhinney DB, Geiger E, Blinder J, Benson DW, Goldmuntz E. McElhinney DB, et al. J Am Coll Cardiol. 2003 Nov 5;42(9):1650-5. doi: 10.1016/j.jacc.2003.05.004. J Am Coll Cardiol. 2003. PMID: 14607454 Free article.

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