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

Year Number of Results
1985 1
1992 1
1994 2
1995 1
1997 2
1998 4
1999 1
2000 3
2001 4
2002 3
2003 2
2004 2
2005 3
2006 4
2007 3
2008 7
2009 5
2010 5
2011 5
2012 1
2013 3
2014 4
2015 13
2016 7
2017 3
2018 7
2019 3
2020 3
2024 0

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Similar articles for PMID: 18241070

92 results

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Page 1
A standard echocardiographic and tissue Doppler study of morphological and functional findings in children with hypertrophic cardiomyopathy compared to those with left ventricular hypertrophy in the setting of Noonan and LEOPARD syndromes.
Cerrato F, Pacileo G, Limongelli G, Gagliardi MG, Santoro G, Digilio MC, Di Salvo G, Ardorisio R, Miele T, Calabrò R. Cerrato F, et al. Cardiol Young. 2008 Dec;18(6):575-80. doi: 10.1017/S104795110800320X. Epub 2008 Oct 9. Cardiol Young. 2008. PMID: 18842161
Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers.
Kumar S, Baldinger SH, Gandjbakhch E, Maury P, Sellal JM, Androulakis AF, Waintraub X, Charron P, Rollin A, Richard P, Stevenson WG, Macintyre CJ, Ho CY, Thompson T, Vohra JK, Kalman JM, Zeppenfeld K, Sacher F, Tedrow UB, Lakdawala NK. Kumar S, et al. J Am Coll Cardiol. 2016 Nov 29;68(21):2299-2307. doi: 10.1016/j.jacc.2016.08.058. J Am Coll Cardiol. 2016. PMID: 27884249 Free article.
Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations.
Digilio MC, Pacileo G, Sarkozy A, Limongelli G, Conti E, Cerrato F, Marino B, Pizzuti A, Calabrò R, Dallapiccola B. Digilio MC, et al. Birth Defects Res A Clin Mol Teratol. 2004 Feb;70(2):95-8. doi: 10.1002/bdra.10148. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 14991917
92 results