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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
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1992 1
1993 1
1997 1
1998 1
2001 1
2003 1
2004 2
2005 4
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2009 1
2011 3
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32 results

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Page 1
Improvement in Interstage Survival in a National Pediatric Cardiology Learning Network.
Anderson JB, Beekman RH 3rd, Kugler JD, Rosenthal GL, Jenkins KJ, Klitzner TS, Martin GR, Neish SR, Brown DW, Mangeot C, King E, Peterson LE, Provost L, Lannon C; National Pediatric Cardiology Quality Improvement Collaborative. Anderson JB, et al. Among authors: neish sr. Circ Cardiovasc Qual Outcomes. 2015 Jul;8(4):428-36. doi: 10.1161/CIRCOUTCOMES.115.001956. Epub 2015 Jun 9. Circ Cardiovasc Qual Outcomes. 2015. PMID: 26058717 Review. No abstract available.
Sudden death in congenital heart disease.
Pelech AN, Neish SR. Pelech AN, et al. Among authors: neish sr. Pediatr Clin North Am. 2004 Oct;51(5):1257-71. doi: 10.1016/j.pcl.2004.04.013. Pediatr Clin North Am. 2004. PMID: 15331283 Review.
Report of the National Heart, Lung, and Blood Institute Working Group on research in adult congenital heart disease.
Williams RG, Pearson GD, Barst RJ, Child JS, del Nido P, Gersony WM, Kuehl KS, Landzberg MJ, Myerson M, Neish SR, Sahn DJ, Verstappen A, Warnes CA, Webb CL; National Heart, Lung, and Blood Institute Working Group on research in adult congenital heart disease. Williams RG, et al. Among authors: neish sr. J Am Coll Cardiol. 2006 Feb 21;47(4):701-7. doi: 10.1016/j.jacc.2005.08.074. Epub 2006 Jan 26. J Am Coll Cardiol. 2006. PMID: 16487831 Free article.
Databases for Congenital Heart Defect Public Health Studies Across the Lifespan.
Riehle-Colarusso TJ, Bergersen L, Broberg CS, Cassell CH, Gray DT, Grosse SD, Jacobs JP, Jacobs ML, Kirby RS, Kochilas L, Krishnaswamy A, Marelli A, Pasquali SK, Wood T, Oster ME; Congenital Heart Public Health Consortium. Riehle-Colarusso TJ, et al. J Am Heart Assoc. 2016 Oct 26;5(11):e004148. doi: 10.1161/JAHA.116.004148. J Am Heart Assoc. 2016. PMID: 27912209 Free PMC article. Review. No abstract available.
Spectrum of CHD7 mutations in 110 individuals with CHARGE syndrome and genotype-phenotype correlation.
Lalani SR, Safiullah AM, Fernbach SD, Harutyunyan KG, Thaller C, Peterson LE, McPherson JD, Gibbs RA, White LD, Hefner M, Davenport SL, Graham JM, Bacino CA, Glass NL, Towbin JA, Craigen WJ, Neish SR, Lin AE, Belmont JW. Lalani SR, et al. Among authors: neish sr. Am J Hum Genet. 2006 Feb;78(2):303-14. doi: 10.1086/500273. Epub 2005 Dec 29. Am J Hum Genet. 2006. PMID: 16400610 Free PMC article.
32 results