Second natural history study of congenital heart defects

Management strategy for very mild aortic valve stenosis.

Pediatric cardiology·2006

Growth patterns of hyperlipidemic children enrolled in a preventive cardiovascular health clinic.

Clinical pediatrics·1994

Arrhythmias in patients with valvar aortic stenosis, valvar pulmonary stenosis, and ventricular septal defect. Results of 24-hour ECG monitoring.

Circulation·1993

Bacterial endocarditis in patients with aortic stenosis, pulmonary stenosis, or ventricular septal defect.

Circulation·1993

Cardiorespiratory responses to exercise of patients with aortic stenosis, pulmonary stenosis, and ventricular septal defect.

Circulation·1993

Second natural history study of congenital heart defects. Results of treatment of patients with ventricular septal defects.

Circulation·1993

Immune Checkpoint Inhibitor Myocarditis and Myotoxicity.

Circulation·2026

Impaired Glycolysis Leads to Defective Efferocytosis and Impaired Plaque Resolution in Tet2 Clonal Hematopoiesis.

Circulation·2026

Macrotroponin Complexes and Risk of Cardiovascular Events.

Circulation·2026

Arrhythmic Risk Stratification According to LGE Corridors and Genetics in Nonischemic Dilated Cardiomyopathy.

Circulation·2026

Infective Endocarditis: Diagnosis, Antibiotic Therapy, and Management: A Scientific Statement From the American Heart Association.

Circulation·2026

An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy.

Circulation·2026

Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.

Molecular biology and evolution·2026

Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.

Brain communications·2026

Disrupting peripheral serotonin synthesis drives sex-specific alterations in sociability and cognition, and reshapes the gut-immune-brain axis.

Brain, behavior, and immunity·2026

Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.

Legal medicine (Tokyo, Japan)·2026

LINE-1 repeats are a defining feature of the Xce.

Proceedings of the National Academy of Sciences of the United States of America·2026

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

JCI insight·2026

Related Experiment Videos

Second natural history study of congenital heart defects

Related Concept Videos

Management strategy for very mild aortic valve stenosis.

Growth patterns of hyperlipidemic children enrolled in a preventive cardiovascular health clinic.

Arrhythmias in patients with valvar aortic stenosis, valvar pulmonary stenosis, and ventricular septal defect. Results of 24-hour ECG monitoring.

Bacterial endocarditis in patients with aortic stenosis, pulmonary stenosis, or ventricular septal defect.

Cardiorespiratory responses to exercise of patients with aortic stenosis, pulmonary stenosis, and ventricular septal defect.

Second natural history study of congenital heart defects. Results of treatment of patients with ventricular septal defects.

Immune Checkpoint Inhibitor Myocarditis and Myotoxicity.

Impaired Glycolysis Leads to Defective Efferocytosis and Impaired Plaque Resolution in Tet2 Clonal Hematopoiesis.

Macrotroponin Complexes and Risk of Cardiovascular Events.

Arrhythmic Risk Stratification According to LGE Corridors and Genetics in Nonischemic Dilated Cardiomyopathy.

Infective Endocarditis: Diagnosis, Antibiotic Therapy, and Management: A Scientific Statement From the American Heart Association.

An Updated Evidence Assessment of the Genetic Causes of Dilated Cardiomyopathy.

Widespread male-female expression imbalance of X-linked genes across phrynosomatid lizards.

Multimodal quantitative MRI finds early brain changes in asymptomatic X-linked adrenoleukodystrophy.

Disrupting peripheral serotonin synthesis drives sex-specific alterations in sociability and cognition, and reshapes the gut-immune-brain axis.

Fatal ascending aortic dissection in a 12-year-old boy with previously undiagnosed Loeys-Dietz syndrome: A molecular autopsy case.

LINE-1 repeats are a defining feature of the Xce.

A familial case of FLAD1 protein deficiency associated with impaired adrenal steroidogenesis.

Related Experiment Videos

Second natural history study of congenital heart defects

Related Concept Videos

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