Phenylketonuria: Old disease, new approach to treatment

nork Levy, Harvey L.
Argitaratua 1999

Early diagnosis and prevention of genetic diseases

nork Levy, Harvey L.
Argitaratua 1977

Newborn screening: the genomic challenge

nork Levy, Harvey L
Argitaratua 2014

Robert Guthrie and the Trials and Tribulations of Newborn Screening

nork Levy, Harvey L.
Argitaratua izan da Int J Neonatal Screen (2021)

Ethical and Psychosocial Implications of Genomic Newborn Screening

nork Levy, Harvey L.
Argitaratua izan da Int J Neonatal Screen (2021)

Is Melatonin Synthesis a New Biomarker for the Pathogenesis and Treatment of Phenylketonuria?

nork Cederbaum, Stephen, Levy, Harvey L.
Argitaratua izan da J Pediatr (2013)

The Contractile and Control Sites of Natural Actomyosin

nork Levy, Harvey M., Ryan, Elizabeth M.
Argitaratua 1967

PURIFIED MUSCLE PROTEINS AND THE WALKING RATE OF ANTS

nork Levy, Harvey M., Sharon, Nathan, Koshland, D. E.
Argitaratua 1959

The Complexity of Newborn Screening Follow-Up in Phenylketonuria

nork Hecht, Leah E., Wessel, Ann E., Levy, Harvey L., Berry, Gerard T.
Argitaratua izan da JIMD Rep (2014)

Discontinuation of Pegvaliase therapy during maternal PKU pregnancy and postnatal breastfeeding: A case report

nork Rohr, Fran, Kritzer, Amy, Harding, Cary O., Viau, Krista, Levy, Harvey L.
Argitaratua izan da Mol Genet Metab Rep (2020)

A missense mutation (Q279R) in the Fumarylacetoacetate Hydrolase gene, responsible for hereditary tyrosinemia, acts as a splicing mutation

nork Dreumont, Natacha, Poudrier, Jacques A, Bergeron, Anne, Levy, Harvey L, Baklouti, Faouzi, Tanguay, Robert M
Argitaratua 2001

Untargeted metabolomics identifies unique though benign biochemical changes in patients with pathogenic variants in UROC1

nork Glinton, Kevin E., Levy, Harvey L., Kennedy, Adam D., Pappan, Kirk L., Elsea, Sarah H.
Argitaratua izan da Mol Genet Metab Rep (2018)

Metabolomic Markers of Essential Fatty Acids, Carnitine, and Cholesterol Metabolism in Adults and Adolescents with Phenylketonuria

nork Stroup, Bridget M, Nair, Nivedita, Murali, Sangita G, Broniowska, Katarzyna, Rohr, Fran, Levy, Harvey L, Ney, Denise M
Argitaratua izan da J Nutr (2018)

First 1.5 years of pegvaliase clinic: Experiences and outcomes

nork Sacharow, Stephanie, Papaleo, Cassandra, Almeida, Kyla, Goodlett, Benjamin, Kritzer, Amy, Levy, Harvey, Martell, Leslie, Wessel, Ann, Viau, Krista
Argitaratua izan da Mol Genet Metab Rep (2020)

Dietary amino acid intakes associated with a low-phenylalanine diet combined with amino acid medical foods and glycomacropeptide medical foods and neuropsychological outcomes in su...

nork Stroup, Bridget M., Murali, Sangita G., Nair, Nivedita, Sawin, Emily A., Rohr, Fran, Levy, Harvey L., Ney, Denise M.
Argitaratua izan da Data Brief (2017)

Metabolomic changes demonstrate reduced bioavailability of tyrosine and altered metabolism of tryptophan via the kynurenine pathway with ingestion of medical foods in phenylketonur...

nork Ney, Denise M., Murali, Sangita G., Stroup, Bridget M., Nair, Nivedita, Sawin, Emily A., Rohr, Fran, Levy, Harvey L
Argitaratua izan da Mol Genet Metab (2017)

A germline or de novo mutation in two families with Gaucher disease: implications for recessive disorders

nork Saranjam, Hamid, Chopra, Sameer S, Levy, Harvey, Stubblefield, Barbara K, Maniwang, Emerson, Cohen, Ian J, Baris, Hagit, Sidransky, Ellen, Tayebi, Nahid
Argitaratua 2013

Glycomacropeptide for nutritional management of phenylketonuria: a randomized, controlled, crossover trial(1)(2)

nork Ney, Denise M, Stroup, Bridget M, Clayton, Murray K, Murali, Sangita G, Rice, Gregory M, Rohr, Frances, Levy, Harvey L
Argitaratua izan da Am J Clin Nutr (2016)

Metabolomic Insights into the Nutritional Status of Adults and Adolescents with Phenylketonuria Consuming a Low-Phenylalanine Diet in Combination with Amino Acid and Glycomacropept...

nork Stroup, Bridget M., Ney, Denise M., Murali, Sangita G., Rohr, Frances, Gleason, Sally T., van Calcar, Sandra C., Levy, Harvey L.
Argitaratua izan da J Nutr Metab (2017)

Methionine Adenosyltransferase I/III Deficiency: Novel Mutationsand Clinical Variations

nork Chamberlin, Margaret E., Ubagai, Tsuneyuki, Mudd, S. Harvey, Thomas, Janet, Pao, Vivian Y., Nguyen, Thien K., Levy, Harvey L., Greene, Carol, Freehauf, Cynthia, Chou, Janice Yang
Argitaratua 2000