Professor of Pediatrics, Boston Children's Hospital

Medical Genetics

Dr. Harvey L. Levy is an expert in the field of Medical Genetics. He graduated from Medical College of Georgia School of Medicine. Harvey Levy is a published doctor and has 36 publications published. The lastest was: 'Maternal Phenylketonuria: Long-term Outcomes in Offspring and Post-pregnancy Maternal Characteristics.'

Publications

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• Hyperphenylalaninemia and the genomic revolution.
• Maternal Phenylketonuria: Long-term Outcomes in Offspring and Post-pregnancy Maternal Characteristics.
• Adherence to tetrahydrobiopterin therapy in patients with phenylketonuria.
• The Complexity of Newborn Screening Follow-Up in Phenylketonuria.
• Phenylketonuria Scientific Review Conference: State of the science and future research needs.
• Newborn screening: the genomic challenge.
• Management of a Woman With Maple Syrup Urine Disease During Pregnancy, Delivery, and Lactation.
• Newborn Screening for Glutaric Aciduria-II: The New England Experience.
• 50 years ago in the journalof pediatrics galactosemia: then and now.
• Newborn screening conditions: What we know, what we do not know, and how we will know it.
• Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening.
• Mutations in the phenylalanine hydroxylase gene identified in 95 patients with phenylketonuria using novel systems of mutation scanning and specific genotyping based u...
• The use of betaine in the treatment of elevated homocysteine.
• Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12.
• Newborn screening for metabolic disorders.
• Fetal fatty acid oxidation defects and maternal liver disease in pregnancy.
• The clinical aspects of newborn screening: importance of newborn screening follow-up.
• Metabolic disorders in the center of genetic medicine.
• Laboratory diagnosis of 1,4-BD and GHB overdose by routine urine organic acid analysis.
• Brief report: Predictors of parenting stress among parents of children with biochemical genetic disorders.
• Expanded screening of newborns for genetic disorders.
• Historical background for the maternal PKU syndrome.
• Impact of the phenylalanine hydroxylase gene on maternal phenylketonuria outcome.
• Pregnancy experiences in the woman with mild hyperphenylalaninemia.
• Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.
• Lessons from the past--looking to the future. Newborn screening.
• Molecular genetic and potential biochemical characteristics of patients with T-protein deficiency as a cause of glycine encephalopathy (NKH).
• Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap.
• Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edema.
• Expanded newborn screening using tandem mass spectrometry.
• Phenylketonuria.
• Pericardial effusion in primary systemic carnitine deficiency.
• Krabbe disease: severe neonatal presentation with a family history of multiple sclerosis.
• Neonatal screening for medium--chain acyl-CoA dehydrogenase deficiency.
• Efficacy of sapropterin dihydrochloride (tetrahydrobiopterin, 6R-BH4) for reduction of phenylalanine concentration in patients with phenylketonuria: a phase III random...

Schools

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• Medical College of Georgia

• Boston City Hospital

• Columbia Presby

• Johns Hopkins Hospital

• Massachusetts General Hospital

Doctors Specialties

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• Clinical Biochemical Genetics
• Pediatrics
• Medical Genetics

Accepted Insurances

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Education

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• Boston University Medical Center
• Johns Hopkins University
• New York Presbyterian Hospital - Columbia Campus
• Medical College of Georgia School of Medicine

Hospital

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• Boston Children's Hospital

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