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Pediatrics, ISSN 0031-4005, 04/2007, Volume 119, Issue 4, pp. 722 - 733
OBJECTIVES. We sought to determine the clinical spectrum, survival, and long-term functional outcome of a cohort of pediatric patients with mitochondrial... 
Functional status | Long-term outcome | Mitochondrial diseases | OXIDATIVE-PHOSPHORYLATION | C-OXIDASE DEFICIENCY | CARDIOMYOPATHY | PYRUVATE-DEHYDROGENASE COMPLEX | CHILDREN | SKELETAL-MUSCLE | mitochondrial diseases | functional status | ELECTROPHORESIS | long-term outcome | PEDIATRICS | LACTIC-ACIDOSIS | MUTATIONS | RESPIRATORY-CHAIN DISORDERS | Follow-Up Studies | Mitochondrial Encephalomyopathies - mortality | Humans | Child, Preschool | Infant | Male | Optic Atrophy, Hereditary, Leber - genetics | Cause of Death | DNA, Mitochondrial - genetics | Time Factors | DNA Fragmentation | Female | Mitochondrial Myopathies - mortality | Retrospective Studies | MELAS Syndrome - therapy | Mitochondrial Myopathies - diagnosis | Optic Atrophy, Hereditary, Leber - diagnosis | Child | Infant, Newborn | Optic Atrophy, Hereditary, Leber - mortality | Mitochondrial Diseases - genetics | Severity of Illness Index | Proportional Hazards Models | Probability | Mitochondrial Encephalomyopathies - diagnosis | Mitochondrial Myopathies - genetics | Mitochondrial Encephalomyopathies - therapy | MELAS Syndrome - diagnosis | Survival Analysis | MELAS Syndrome - mortality | Mitochondrial Diseases - mortality | Mitochondrial Diseases - diagnosis | Cohort Studies | Causes of | Care and treatment | Diagnosis | Risk factors | Babies | Pediatrics | Mitochondrial DNA | Genetic disorders | Genes | Clinical outcomes | Index Medicus | Abridged Index Medicus
Journal Article
Acta Paediatrica, ISSN 0803-5253, 05/2016, Volume 105, Issue 5, pp. 549 - 554
Journal Article
Cardiology Journal, ISSN 1897-5593, 2017, Volume 24, Issue 1, pp. 101 - 104
FOLLOW-UP | DEFECTS | CARDIAC & CARDIOVASCULAR SYSTEMS | DILATED CARDIOMYOPATHY | Lipid Metabolism, Inborn Errors - mortality | Lipid Metabolism, Inborn Errors - genetics | Arrhythmias, Cardiac - mortality | Humans | Child, Preschool | Rhabdomyolysis - complications | Male | Rhabdomyolysis - mortality | Cardiomyopathy, Hypertrophic - therapy | Child | Cardiomyopathy, Dilated - mortality | Genetic Predisposition to Disease | Arrhythmias, Cardiac - therapy | Risk Factors | Nervous System Diseases - diet therapy | Nervous System Diseases - complications | Phenotype | Diet, Fat-Restricted | Adolescent | Arrhythmias, Cardiac - diagnosis | Lipid Metabolism, Inborn Errors - complications | Mutation | Cardiomyopathy, Dilated - therapy | Mitochondrial Trifunctional Protein - deficiency | Lipid Metabolism, Inborn Errors - diet therapy | Mitochondrial Trifunctional Protein, alpha Subunit - genetics | Infant | Nervous System Diseases - genetics | Cardiomyopathies - genetics | Rhabdomyolysis - diet therapy | Cardiomyopathies - mortality | Female | Mitochondrial Myopathies - mortality | Cardiomyopathy, Hypertrophic - diagnostic imaging | Cardiomyopathy, Hypertrophic - etiology | Mitochondrial Trifunctional Protein - genetics | Nervous System Diseases - mortality | Cardiomyopathies - diet therapy | Mitochondrial Myopathies - complications | Treatment Outcome | Arrhythmias, Cardiac - etiology | Mitochondrial Myopathies - diet therapy | Triglycerides - administration & dosage | Cardiomyopathy, Dilated - diagnostic imaging | Cardiomyopathy, Hypertrophic - mortality | Mitochondrial Myopathies - genetics | Cardiomyopathy, Dilated - etiology | Rhabdomyolysis - genetics | Cardiomyopathies - complications | Index Medicus
Journal Article
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 11/2000, Volume 918, Issue 1, pp. 222 - 235
Journal Article
Journal Article
Journal Article
Neurology, ISSN 0028-3878, 09/1999, Volume 53, Issue 4, pp. 855 - 857
Journal Article
Neurology, ISSN 0028-3878, 1998, Volume 51, Issue 4, pp. 1190 - 1193
Journal Article
Medicine, ISSN 1357-3039, 2016, Volume 44, Issue 9, pp. 570 - 575
Abstract About 70,000 people in the UK (around 62 million) have a peripheral neuromuscular disorder, with about one-half of them having a myopathy. They can be... 
Internal Medicine | myotonic dystrophy | muscular dystrophy | facioscapulohumeral muscular dystrophy | inclusion body myositis | myopathy | statins | Dermatomyositis | mitochondrial cytopathy | myositis | polymyositis
Journal Article
Journal Article
Pediatrics, ISSN 0031-4005, 10/2004, Volume 114, Issue 4, pp. 925 - 931
Journal Article
Journal Article