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European Journal of Heart Failure|September 8, 2011
Genetic basis of end-stage hypertrophic cardiomyopathyPablo Garcia-Pavia, Maria E Vázquez, Javier Segovia, et al.
The Biochemical Journal|November 24, 2004
Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA(Lys) geneBelén Bornstein, José Antonio Mas, Clarice Patrono, et al.
European Heart Journal|August 9, 2011
Mitochondrial haplogroups associated with end-stage heart failure and coronary allograft vasculopathy in heart transplant patientsM Esther Gallardo, Pablo García-Pavía, Raquel Chamorro, et al.
Mitochondrion|October 12, 2011
Mitochondrial tRNA valine as a recurrent target for mutations involved in mitochondrial cardiomyopathiesJuan J Arredondo, M Esther Gallardo, Pablo García-Pavía, et al.
European Heart Journal|July 31, 2015
Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fractionEsther González-López, Maria Gallego-Delgado, Gonzalo Guzzo-Merello, et al.
Clinical Biochemistry|December 20, 2008
Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: a case reportRaquel Montero, Jose A Sánchez-Alcázar, Paz Briones, et al.
Revista Espanola De Cardiologia (English Ed.)|April 23, 2020
Clinical profile and outcome of cardiac amyloidosis in a Spanish referral centerÁngela López-Sainz, Aitor Hernandez-Hernandez, Esther Gonzalez-Lopez, et al.
Brain : a Journal of Neurology|December 26, 2007
OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypesPatrizia Amati-Bonneau, Maria Lucia Valentino, Pascal Reynier, et al.
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