Physician

Pediatric Cardiology

Arnold Strauss works in the field of Pediatric Cardiology. He graduated from Washington University School of Medicine in St. Louis. He received awards:"Elected Member". Arnold W. Strauss is a published MD as well. He has 36 publications published. The latest was: Cardiac-specific VLCAD deficiency induces dilated cardiomyopathy and cold intolerance.

Publications

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• Cardiac-specific VLCAD deficiency induces dilated Cardiomyopathy and cold intolerance.
• Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase.
• Spectrum of medium-chain acyl-CoA dehydrogenase deficiency detected by newborn screening.
• Polymorphic ventricular tachycardia and abnormal Ca2+ handling in very-long-chain acyl-CoA dehydrogenase null mice.
• Reye-like syndrome resulting from novel missense mutations in mitochondrial medium- and short-chain l-3-hydroxy-acyl-CoA dehydrogenase.
• Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levels.
• A zebrafish model of human Barth syndrome reveals the essential role of tafazzin in cardiac development and function.
• Pitfalls of neonatal screening for very-long-chain acyl-CoA dehydrogenase deficiency using tandem mass spectrometry.
• Rhabdomyolysis in the military: recognizing late-onset very long-chain acyl Co-A dehydrogenase deficiency.
• Abnormal mitochondrial bioenergetics and Heart rate dysfunction in mice lacking very-long-chain acyl-CoA dehydrogenase.
• Tissue carnitine homeostasis in very-long-chain acyl-CoA dehydrogenase-deficient mice.
• Surprising? Perhaps not. Long-chain fatty acid oxidation during human fetal development.
• Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management.
• Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.
• Improved outcomes of pediatric dilated Cardiomyopathy with utilization of heart transplantation.
• Tandem mass spectrometry in discovery of disorders of the metabolome.
• General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in ei...
• Peripheral neuropathy, episodic myoglobinuria, and respiratory Failure in deficiency of the mitochondrial trifunctional protein.
• Very-long-chain acyl-coenzyme a dehydrogenase deficiency in mice.
• MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiency.
• Human placenta metabolizes fatty acids: implications for fetal fatty acid oxidation disorders and maternal liver Diseases.
• Molecular and phenotypic heterogeneity in mitochondrial trifunctional protein deficiency due to beta-subunit mutations.
• Uniparental disomy of chromosome 2 resulting in lethal trifunctional protein deficiency due to homozygous alpha-subunit mutations.
• Prospective screening for pediatric mitochondrial trifunctional protein defects in pregnancies complicated by liver Disease.
• Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations.
• A novel mutation of late-onset very-long-chain acyl-CoA dehydrogenase deficiency.
• The molecular basis of congenital cardiac Disease.
• Diminished Exercise Capacity and Mitochondrial bc1 Complex Deficiency in Tafazzin-Knockdown Mice.
• Salami science or editorial imperialism?
• Presentation of Pulmonary artery intimal sarcoma in an infant with a history of neonatal valvular pulmonic stenosis.
• Pediatric Cardiomyopathy--a long way to go.
• Early neonatal diagnosis of long-chain 3-hydroxyacyl coenzyme a dehydrogenase and mitochondrial trifunctional protein deficiencies.
• A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency.
• Cardiac and skeletal muscle defects in a mouse model of human Barth syndrome.
• Report of the Tennessee Task Force on Screening Newborn Infants for Critical Congenital Heart Disease.

Schools

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• Washington University St Louis

• St Louis Chldns Hospital

Conditions Treated

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• Aortic Ectasia
• Arrhythmias (incl. Atrial Fibrillation)
• Cardiomegaly
• Cardiomyopathy
• View All

Doctors Specialties

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• Pediatric Cardiology

Accepted Insurances

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Awards

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• Elected Member

Education

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• Washington University School of Medicine in St. Louis

Hospital

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• Cincinnati Children's Hospital Medical Center
• Christ Hospital

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