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Cardiomyopathies

Vascular Endothelial Dysfunction In Diabetic Cardiomyopathy: Pathogenesis and Potential Treatment Targets

Pharmacology / Clinical Trial / Extracellular Matrix / Heart Failure / Protein Structure and Function / CAD / NO / Humans / Age / Hyperglycemia / Basement Membrane / VEGF / Animals / Vascular endothelium / PKC / Structural Change / Lipoprotein(a) / Glucose Transport / Nitric Oxide Synthase / Endothelial cell / Fatty Acid / PPAR / Toll-Like Receptors Therapeutics Pharmacology / MAPK / Cardiomyopathies / NAD / Vascular Endothelial Function / Intracellular Signaling / PARP / Redox Potential / CAD / NO / Humans / Age / Hyperglycemia / Basement Membrane / VEGF / Animals / Vascular endothelium / PKC / Structural Change / Lipoprotein(a) / Glucose Transport / Nitric Oxide Synthase / Endothelial cell / Fatty Acid / PPAR / Toll-Like Receptors Therapeutics Pharmacology / MAPK / Cardiomyopathies / NAD / Vascular Endothelial Function / Intracellular Signaling / PARP / Redox Potential

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Superior vena caval obstruction after complete resolution of cardiac tuberculoma

Magnetic Resonance Imaging / Humans / Female / Clinical Sciences / Adult / Clinical Radiology / Cardiomyopathies / X ray Computed Tomography / Magnetic resonance angiography / Clinical Radiology / Cardiomyopathies / X ray Computed Tomography / Magnetic resonance angiography

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Reparative Effects of Allogeneic Mesenchymal Precursor Cells Delivered Transendocardially in Experimental Nonischemic Cardiomyopathy

Magnetic Resonance Imaging / Treatment Outcome / Stem Cell / Echocardiography / Sheep / Animals / Follow-up studies / Alkaline phosphatase / Myocardium / Fluorescent Protein / Cardiomyopathies / Monoclonal Antibody / Animals / Follow-up studies / Alkaline phosphatase / Myocardium / Fluorescent Protein / Cardiomyopathies / Monoclonal Antibody

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Cardiovascular Magnetic Resonance: Myocardial Perfusion

Cardiology / Kinetics / Quantitative analysis / Visual Analysis / Humans / Motion Tracking / Female / Feasibility Studies / Male / Feature tracking / Magnetic Resonance / Young Adult / Acute Myocardial Infarction / Steady state / Clinical Sciences / Aged / Middle Aged / Observer Variation / Adult / Reproducibility of Results / Quantitative Analysis / Ischemic Heart Disease / Diagnostic Accuracy / Cardiomyopathies / Coronary Artery Disease / Ejection Fraction / Reference Values / Healthy Subjects / Cardiovascular Magnetic Resonance / Predictive value of tests / Confidence Interval / Clinical evaluation / Cardiac Magnetic Resonance Imaging / SHORT-AXIS / Coronary artery / Magnetic resonance image / Motion Tracking / Female / Feasibility Studies / Male / Feature tracking / Magnetic Resonance / Young Adult / Acute Myocardial Infarction / Steady state / Clinical Sciences / Aged / Middle Aged / Observer Variation / Adult / Reproducibility of Results / Quantitative Analysis / Ischemic Heart Disease / Diagnostic Accuracy / Cardiomyopathies / Coronary Artery Disease / Ejection Fraction / Reference Values / Healthy Subjects / Cardiovascular Magnetic Resonance / Predictive value of tests / Confidence Interval / Clinical evaluation / Cardiac Magnetic Resonance Imaging / SHORT-AXIS / Coronary artery / Magnetic resonance image

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Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization

Genetics / Electron Microscopy / Membrane Proteins / Mitochondria / Tomography / Mitochondrial DNA / Humans / Mutation / Female / Male / ATP synthase / Mitochondrial Respiratory Chain / Newborn Infant / Mitochondrial Diseases / Adult / Cardiomyopathies / Human Fibroblasts / Mitochondrion / Mitochondrial DNA / Humans / Mutation / Female / Male / ATP synthase / Mitochondrial Respiratory Chain / Newborn Infant / Mitochondrial Diseases / Adult / Cardiomyopathies / Human Fibroblasts / Mitochondrion

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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ-oxidation

Nursing / Pediatrics / Treatment Outcome / Mitochondria / Pediatric nursing / Adolescent / Liver diseases / High Frequency / Heart Failure / Pregnancy / Humans / Child / Liver Cirrhosis / Liver / Mutation / Female / Male / Hypoglycemia / Fatty Acid Oxidation / Infant / Follow-up studies / Netherlands / Differential Diagnosis / HELLP Syndrome / Phenotype / Clinical Sciences / Newborn Infant / L-carnitine / Questionnaires / Optometry and Ophthalmology / Public health systems and services research / Survival Rate / Fatty Acid / Health surveys / Multienzyme complexes / Cardiomyopathies / Status Epilepticus / Base Sequence / Human Fibroblasts / Clinical Presentation / Clinical Signs / Antiepileptic Drug / Archivos Argentinos De Pediatria / Brain Damage / Age of Onset / Adolescent / Liver diseases / High Frequency / Heart Failure / Pregnancy / Humans / Child / Liver Cirrhosis / Liver / Mutation / Female / Male / Hypoglycemia / Fatty Acid Oxidation / Infant / Follow-up studies / Netherlands / Differential Diagnosis / HELLP Syndrome / Phenotype / Clinical Sciences / Newborn Infant / L-carnitine / Questionnaires / Optometry and Ophthalmology / Public health systems and services research / Survival Rate / Fatty Acid / Health surveys / Multienzyme complexes / Cardiomyopathies / Status Epilepticus / Base Sequence / Human Fibroblasts / Clinical Presentation / Clinical Signs / Antiepileptic Drug / Archivos Argentinos De Pediatria / Brain Damage / Age of Onset

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Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency

Mitochondria / Humans / Fatty acids / Mutation / Male / Fatty Acid Oxidation / Phenotype / Enzyme / Clinical Sciences / L-carnitine / Spectrum / Prognosis / Multienzyme complexes / Cardiomyopathies / Human Fibroblasts / Clinical Presentation / Rhabdomyolysis / Fatty Acid Oxidation / Phenotype / Enzyme / Clinical Sciences / L-carnitine / Spectrum / Prognosis / Multienzyme complexes / Cardiomyopathies / Human Fibroblasts / Clinical Presentation / Rhabdomyolysis

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Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization

Genetics / Electron Microscopy / Membrane Proteins / Mitochondria / Tomography / Mitochondrial DNA / Humans / Mutation / Female / Male / ATP synthase / Mitochondrial Respiratory Chain / Newborn Infant / Mitochondrial Diseases / Adult / Cardiomyopathies / Human Fibroblasts / Mitochondrial DNA / Humans / Mutation / Female / Male / ATP synthase / Mitochondrial Respiratory Chain / Newborn Infant / Mitochondrial Diseases / Adult / Cardiomyopathies / Human Fibroblasts

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Remodelado cardiaco inverso estructural y funcional en pacientes con aleteo auricular típico sometidos a ablación del istmo cavotricuspídeo

Humans / Female / Male / Follow-up studies / Aged / Middle Aged / Catheter ablation / Cardiomyopathies / Atrial Flutter / CTI / LVEF / Middle Aged / Catheter ablation / Cardiomyopathies / Atrial Flutter / CTI / LVEF

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integrales en linea

Probability / Blood Glucose / Hemodynamics / Animals / Male / Heart rate / Clinical Sciences / Rats / Body Weight / Wistar Rats / Cardiomyopathies / Streptozotocin / Diastolic Dysfunction/CHF / Reference Values / Diabetic Rat / Cardiac failure / Time Course / Isoproterenol / Heart rate / Clinical Sciences / Rats / Body Weight / Wistar Rats / Cardiomyopathies / Streptozotocin / Diastolic Dysfunction/CHF / Reference Values / Diabetic Rat / Cardiac failure / Time Course / Isoproterenol

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Traitement actuel de l’amylose AL

Kidney transplantation / Amyloid / Dexamethasone / Humans / Renal failure / Heart Disease / Gold Standard / Boronic Acids / Prognosis / Biological markers / Combination drug therapy / Cardiomyopathies / Heart Transplantation / Chronic Kidney Failure / Light chain / Immunoglobulin / Thalidomide / Amyloidosis / Renal Dialysis / Nephrotic syndrome / Néphrologie / Heart Disease / Gold Standard / Boronic Acids / Prognosis / Biological markers / Combination drug therapy / Cardiomyopathies / Heart Transplantation / Chronic Kidney Failure / Light chain / Immunoglobulin / Thalidomide / Amyloidosis / Renal Dialysis / Nephrotic syndrome / Néphrologie

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Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization

Genetics / Electron Microscopy / Membrane Proteins / Mitochondria / Tomography / Mitochondrial DNA / Humans / Mutation / Female / Male / ATP synthase / Mitochondrial Respiratory Chain / Newborn Infant / Mitochondrial Diseases / Adult / Cardiomyopathies / Human Fibroblasts / Mitochondrial DNA / Humans / Mutation / Female / Male / ATP synthase / Mitochondrial Respiratory Chain / Newborn Infant / Mitochondrial Diseases / Adult / Cardiomyopathies / Human Fibroblasts

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Magnetic resonance spectroscopy evidence of abnormal cardiac energetics in Xp21 muscular dystrophy

Signal Processing / Magnetic Resonance Spectroscopy / Energy Metabolism / Phosphorus / Cardiac Hypertrophy / Humans / Left Ventricular Assist Device / Muscular Dystrophy / Female / Male / Duchenne Muscular Dystrophy / Dilated cardiomyopathy / Middle Aged / Skeletal Muscle / Adult / Myocardium / Public health systems and services research / Cardiomyopathies / Left Ventricular Function / Chemical Shift Imaging / Adenosine Triphosphate / The American / Becker Muscular Dystrophy (BMD) / Phosphocreatine / Humans / Left Ventricular Assist Device / Muscular Dystrophy / Female / Male / Duchenne Muscular Dystrophy / Dilated cardiomyopathy / Middle Aged / Skeletal Muscle / Adult / Myocardium / Public health systems and services research / Cardiomyopathies / Left Ventricular Function / Chemical Shift Imaging / Adenosine Triphosphate / The American / Becker Muscular Dystrophy (BMD) / Phosphocreatine

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Cuantificación de la función, perfusión y realce tardío del ventrículo izquierdo no compactado mediante resonancia magnética

Magnetic Resonance Imaging / Adolescent / Humans / Left Ventricular Assist Device / Female / Male / Young Adult / Aged / Middle Aged / Adult / Congenital malformation / Coronary Circulation / Cardiomyopathies / Left Ventricle / Radiología / Male / Young Adult / Aged / Middle Aged / Adult / Congenital malformation / Coronary Circulation / Cardiomyopathies / Left Ventricle / Radiología

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Abnormal in vivo myocardial energy substrate uptake in diet-induced type 2 diabetic cardiomyopathy in rats

Type 2 Diabetes / Energy Metabolism / Biological Sciences / Heart Failure / Glucose / Insulin / Animals / Male / Heart / American / Triglycerides / Rats / Myocardium / Analysis of Variance / Wistar Rats / Cardiomyopathies / Enzyme Linked Immunosorbent Assay / Insulin / Animals / Male / Heart / American / Triglycerides / Rats / Myocardium / Analysis of Variance / Wistar Rats / Cardiomyopathies / Enzyme Linked Immunosorbent Assay

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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: A severe fatty acid oxidation disorder

Liver diseases / Humans / Male / Hypoglycemia / Fatty Acid Oxidation / Differential Diagnosis / Newborn Infant / L-carnitine / Public health systems and services research / Cardiomyopathies / Differential Diagnosis / Newborn Infant / L-carnitine / Public health systems and services research / Cardiomyopathies

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