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Skeletal muscle involvement in cardiomyopathies.
Limongelli G, D'Alessandro R, Maddaloni V, Rea A, Sarkozy A, McKenna WJ. Limongelli G, et al. Among authors: sarkozy a. J Cardiovasc Med (Hagerstown). 2013 Dec;14(12):837-61. doi: 10.2459/JCM.0b013e3283641c69. J Cardiovasc Med (Hagerstown). 2013. PMID: 24149064 Review.
Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome.
Limongelli G, Pacileo G, Marino B, Digilio MC, Sarkozy A, Elliott P, Versacci P, Calabro P, De Zorzi A, Di Salvo G, Syrris P, Patton M, McKenna WJ, Dallapiccola B, Calabro R. Limongelli G, et al. Among authors: sarkozy a. Am J Cardiol. 2007 Aug 15;100(4):736-41. doi: 10.1016/j.amjcard.2007.03.093. Epub 2007 Jun 27. Am J Cardiol. 2007. PMID: 17697839
Trisomy 18 and hypertrophy cardiomyopathy in an 18-year-old woman.
Limongelli G, Pacileo G, Melis D, Calabro' P, Digilio MC, Sarkozy A, Maddaloni V, Capozzi G, Sebastio G, Andria G, Calabro' R. Limongelli G, et al. Among authors: sarkozy a. Am J Med Genet A. 2008 Feb 1;146A(3):327-9. doi: 10.1002/ajmg.a.32149. Am J Med Genet A. 2008. PMID: 18203191 No abstract available.
LEOPARD syndrome: clinical diagnosis in the first year of life.
Digilio MC, Sarkozy A, de Zorzi A, Pacileo G, Limongelli G, Mingarelli R, Calabrò R, Marino B, Dallapiccola B. Digilio MC, et al. Among authors: sarkozy a. Am J Med Genet A. 2006 Apr 1;140(7):740-6. doi: 10.1002/ajmg.a.31156. Am J Med Genet A. 2006. PMID: 16523510
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. Among authors: sarkozy a. 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
345 results