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One or more keywords matched the following items that are connected to Levy, Harvey
Item TypeName
Academic Article Lessons from the past--looking to the future. Newborn screening.
Academic Article Krabbe disease: severe neonatal presentation with a family history of multiple sclerosis.
Academic Article Neonatal screening for medium--chain acyl-CoA dehydrogenase deficiency.
Academic Article Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.
Academic Article Pregnancy experiences in the woman with mild hyperphenylalaninemia.
Academic Article Expanded newborn screening using tandem mass spectrometry.
Academic Article The adult galactosemic phenotype.
Academic Article Molecular genetic and potential biochemical characteristics of patients with T-protein deficiency as a cause of glycine encephalopathy (NKH).
Academic Article Infantile hypermethioninemia and hyperhomocysteinemia due to high methionine intake: a diagnostic trap.
Academic Article Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12.
Academic Article Newborn screening of lysosomal storage disorders.
Academic Article Fetal fatty acid oxidation defects and maternal liver disease in pregnancy.
Academic Article Newborn screening conditions: What we know, what we do not know, and how we will know it.
Academic Article The Maternal Phenylketonuria International Study: 1984-2002.
Academic Article Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edema.
Academic Article Mutations in the phenylalanine hydroxylase gene identified in 95 patients with phenylketonuria using novel systems of mutation scanning and specific genotyping based upon thermal melt profiles.
Academic Article Expanded screening of newborns for genetic disorders.
Academic Article Newborn screening for metabolic disorders.
Academic Article The clinical aspects of newborn screening: importance of newborn screening follow-up.
Academic Article Metabolic disorders in the center of genetic medicine.
Academic Article Sudden death in medium chain acyl-coenzyme a dehydrogenase deficiency (MCADD) despite newborn screening.
Concept Infant, Newborn
Concept Infant, Newborn, Diseases
Concept Neonatal Screening
Academic Article Phenylketonuria.
Academic Article Genomics in newborn screening.
Academic Article Newborn screening: the genomic challenge.
Academic Article Phenylketonuria Scientific Review Conference: state of the science and future research needs.
Academic Article The complexity of newborn screening follow-up in phenylketonuria.
Academic Article Long-term outcome of expanded newborn screening at Boston children's hospital: benefits and challenges in defining true disease.
Academic Article The BabySeq project: implementing genomic sequencing in newborns.
Academic Article Phenylalanine hydroxylase genotype-phenotype associations in the United States: A single center study.
Academic Article Can Newborn Screening for Vitamin B12 Deficiency be Incorporated into All Newborn Screening Programs?
Academic Article Ethical and Psychosocial Implications of Genomic Newborn Screening.
Academic Article Robert Guthrie and the Trials and Tribulations of Newborn Screening.
Search Criteria
  • Newborn
  • screening
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.