Mitochondrial pathology in cardiac failure

[1] Apoptosis in skeletal myocytes of patients with chronic heart failure is associated with exercise intolerance [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 33 (04) : 959 - 965

[2] PROGNOSTIC IMPLICATIONS OF NOVEL BETA-CARDIAC MYOSIN HEAVY-CHAIN GENE-MUTATIONS THAT CAUSE FAMILIAL HYPERTROPHIC CARDIOMYOPATHY [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (01) : 280 - 285

[3] CARDIAC INVOLVEMENT IN MITOCHONDRIAL DISEASES - A STUDY ON 17 PATIENTS WITH DOCUMENTED MITOCHONDRIAL-DNA DEFECTS [J]. CIRCULATION, 1995, 91 (04) : 955 - 961

[4] DELETION OF MITOCHONDRIAL-DNA IN THE ENDOMYOCARDIAL BIOPSY SAMPLE FROM A PATIENT WITH KEARNS-SAYRE SYNDROME [J]. EUROPEAN HEART JOURNAL, 1992, 13 (12) : 1718 - 1719

[5] Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy [J]. AMERICAN JOURNAL OF PATHOLOGY, 1998, 153 (05) : 1501 - 1510

[6] Coexistence of mitochondrial DNA and β myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure [J]. HEART, 1998, 80 (06) : 548 - 558

[7] Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin [J]. SCIENCE, 1997, 276 (5319) : 1709 - 1712

[8] Myocardial oxygenation at high workstates in hearts with left ventricular hypertrophy [J]. CARDIOVASCULAR RESEARCH, 1999, 42 (03) : 616 - 626

[9] BALABAN RS, 1990, AM J PHYSIOL, V258, P377

[10] Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy [J]. NEUROLOGY, 1996, 46 (05) : 1329 - 1334

[1] Apoptosis in skeletal myocytes of patients with chronic heart failure is associated with exercise intolerance [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 33 (04) : 959 - 965

[2] PROGNOSTIC IMPLICATIONS OF NOVEL BETA-CARDIAC MYOSIN HEAVY-CHAIN GENE-MUTATIONS THAT CAUSE FAMILIAL HYPERTROPHIC CARDIOMYOPATHY [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (01) : 280 - 285

[3] CARDIAC INVOLVEMENT IN MITOCHONDRIAL DISEASES - A STUDY ON 17 PATIENTS WITH DOCUMENTED MITOCHONDRIAL-DNA DEFECTS [J]. CIRCULATION, 1995, 91 (04) : 955 - 961

[4] DELETION OF MITOCHONDRIAL-DNA IN THE ENDOMYOCARDIAL BIOPSY SAMPLE FROM A PATIENT WITH KEARNS-SAYRE SYNDROME [J]. EUROPEAN HEART JOURNAL, 1992, 13 (12) : 1718 - 1719

[5] Mitochondrial DNA mutations and mitochondrial abnormalities in dilated cardiomyopathy [J]. AMERICAN JOURNAL OF PATHOLOGY, 1998, 153 (05) : 1501 - 1510

[6] Coexistence of mitochondrial DNA and β myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure [J]. HEART, 1998, 80 (06) : 548 - 558

[7] Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin [J]. SCIENCE, 1997, 276 (5319) : 1709 - 1712

[8] Myocardial oxygenation at high workstates in hearts with left ventricular hypertrophy [J]. CARDIOVASCULAR RESEARCH, 1999, 42 (03) : 616 - 626

[9] BALABAN RS, 1990, AM J PHYSIOL, V258, P377

[10] Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy [J]. NEUROLOGY, 1996, 46 (05) : 1329 - 1334