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barth-syndrome (125) 125
barth syndrome (98) 98
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cardiomyopathy (79) 79
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dilated cardiomyopathy (37) 37
pediatrics (37) 37
membrane lipids (35) 35
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myocardium - pathology (27) 27
adult (26) 26
linked cardioskeletal myopathy (26) 26
article (25) 25
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barth syndrome - metabolism (24) 24
3-methylglutaconic aciduria (23) 23
heart diseases (23) 23
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myocardium (22) 22
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heart ventricles - pathology (20) 20
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cardiomyopathy, dilated - genetics (19) 19
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respiratory-chain (19) 19
transcription factors - metabolism (19) 19
genetic disorders (18) 18
respiratory-chain supercomplexes (18) 18
biochemistry, general (17) 17
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saccharomyces-cerevisiae (17) 17
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hypertrophic cardiomyopathy (16) 16
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Journal of biological chemistry, ISSN 0021-9258, 2011, Volume 286, Issue 2, pp. 899 - 908
Journal Article
Circulation, ISSN 0009-7322, 08/2017, Volume 136, Issue 13, pp. e200 - e231
For many neuromuscular diseases (NMDs), cardiac disease represents a major cause of morbidity and mortality. The management of cardiac disease in NMDs is made... 
Neuromuscular disease | Pediatrics | Cardiomyopathy | Muscular dystrophy | AHA Scientific Statements | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOVASCULAR MAGNETIC-RESONANCE | MECHANICAL CIRCULATORY SUPPORT | neuromuscular disease | CONVERTING ENZYME-INHIBITORS | LUNG TRANSPLANTATION GUIDELINES | LEFT-VENTRICULAR NONCOMPACTION | muscular dystrophy | pediatrics | CHEYNE-STOKES RESPIRATION | LAMIN A/C GENE | PERIPHERAL VASCULAR DISEASE | DUCHENNE MUSCULAR-DYSTROPHY | MYOCARDIAL DELAYED ENHANCEMENT | cardiomyopathy | CARDIOSELECTIVE BETA-BLOCKERS | Myotonic Dystrophy - metabolism | Barth Syndrome - metabolism | Friedreich Ataxia - pathology | Myotonic Dystrophy - diagnosis | United States | Humans | Myopathies, Structural, Congenital - genetics | Neuromuscular Diseases - pathology | Barth Syndrome - pathology | Myotonic Dystrophy - pathology | Muscular Dystrophy, Emery-Dreifuss - diagnosis | Cardiomyopathies - diagnosis | Neuromuscular Diseases - diagnosis | Muscular Dystrophies, Limb-Girdle - pathology | Friedreich Ataxia - metabolism | Muscular Dystrophies, Limb-Girdle - diagnosis | Muscular Diseases - metabolism | Risk Factors | Friedreich Ataxia - diagnosis | Muscular Dystrophy, Emery-Dreifuss - pathology | Cardiomyopathies - pathology | Muscular Dystrophy, Duchenne - pathology | Muscular Diseases - pathology | Barth Syndrome - diagnosis | American Heart Association | Muscular Diseases - diagnosis | Muscular Dystrophy, Emery-Dreifuss - metabolism | Muscular Dystrophies, Limb-Girdle - metabolism | Barth Syndrome - genetics | Neuromuscular Diseases - complications | Myopathies, Structural, Congenital - pathology | Cardiomyopathies - complications | Myopathies, Structural, Congenital - diagnosis | Muscular Dystrophy, Duchenne - metabolism | Myopathies, Structural, Congenital - metabolism | Muscular Dystrophy, Duchenne - diagnosis | Index Medicus | Abridged Index Medicus
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 08/2013, Volume 1832, Issue 8, pp. 1194 - 1206
Journal Article
Journal of Lipid Research, ISSN 0022-2275, 05/2013, Volume 54, Issue 5, pp. 1312 - 1325
Journal Article
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 11/2018, Volume 1864, Issue 11, pp. 3650 - 3658
Journal Article
Prenatal diagnosis, ISSN 0197-3851, 2010, Volume 30, Issue 10, pp. 970 - 976
OBJECTIVE: Barth Syndrome (BTHS) is an X-linked multisystem disorder (OMIM 302060) usually diagnosed in infancy and characterized by cardiac problems [dilated... 
Perinatal | Barth syndrome | Hydrops | Neonatal | Fetal | GENE-MUTATIONS | neonatal | hydrops | 3-METHYLGLUTACONIC ACIDURIA | G4.5 GENE | fetal | ACUTE METABOLIC DECOMPENSATION | MASS-SPECTROMETRY | OBSTETRICS & GYNECOLOGY | LEFT-VENTRICULAR NONCOMPACTION | CARDIOSKELETAL MYOPATHY | CARDIAC TRANSPLANTATION | perinatal | LYMPHOBLAST MITOCHONDRIA | GENETICS & HEREDITY | TAZ GENE | Barth Syndrome - epidemiology | Cardiomyopathy, Dilated - pathology | Isolated Noncompaction of the Ventricular Myocardium - genetics | Humans | Isolated Noncompaction of the Ventricular Myocardium - epidemiology | Male | Stillbirth - genetics | Isolated Noncompaction of the Ventricular Myocardium - pathology | Fetal Diseases - genetics | Barth Syndrome - pathology | Endocardial Fibroelastosis - genetics | Fetal Diseases - epidemiology | Endocardial Fibroelastosis - epidemiology | Female | Cardiolipins - blood | Cardiomyopathy, Dilated - genetics | Chromosomes, Human, X - genetics | Cardiomyopathy, Dilated - epidemiology | Lysophospholipids - blood | Biomarkers - blood | Transcription Factors - genetics | Sequence Analysis, DNA | Barth Syndrome - genetics | Pedigree | Fetal Death - epidemiology | Fetal Diseases - pathology | Fetal Death - genetics | Sex Factors | Stillbirth - epidemiology | United Kingdom - epidemiology | Cohort Studies | Endocardial Fibroelastosis - pathology | Heart | Edema | Neonates | Growth rate | Cardiomyopathy | Fetuses | X chromosome | Infants | Hypoglycemia | aciduria | Stress | Mitochondria | Prenatal diagnosis | Dilated cardiomyopathy | Children | Ventricle | Electron transport | Lactic acidosis | Neutropenia | Index Medicus | Original Paper
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 01/2014, Volume 289, Issue 4, pp. 2250 - 2259
Journal Article