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Familial Dilated Cardiomyopathy and Isolated Left Ventricular Noncompaction Associated With Lamin A/C Gene Mutations
(Elsevier, 2004-06-23)
[Abstract] LMNA mutations have been associated with familial or sporadic dilated cardiomyopathy (DC), with or without conduction system disease. We studied the LMNA gene in 67 consecutive patients with DC (18 had familial ...
Sirolimus treatment of left ventricular hypertrophy: who, and when?
(Oxford, 2008-10-19)
Gene expression profiling for monitoring graft rejection in heart transplant recipients
(Elsevier, 2009-08-26)
[Abstract] Heart transplantation is a life-prolonging therapy for many patients with stage D heart failure and other forms of advanced heart disease. However, graft rejection and/or immunosuppression-related side effects ...