Levy HL - Search Results

1

Rapid diagnosis of homocystinuria and other hypermethioninemias from newborns' blood spots by tandem mass spectrometry.

Chace DH, Hillman SL, Millington DS, Kahler SG, Adam BW, Levy HL. Chace DH, et al. Among authors: levy hl. Clin Chem. 1996 Mar;42(3):349-55. Clin Chem. 1996. PMID: 8598094

2

Newborn screening by tandem mass spectrometry: a new era.

Levy HL. Levy HL. Clin Chem. 1998 Dec;44(12):2401-2. Clin Chem. 1998. PMID: 9836702 No abstract available.

3

Comparison of erythrocyte uridine sugar nucleotide levels in normals, classic galactosemics, and patients with other metabolic disorders.

Gibson JB, Reynolds RA, Palmieri MJ, Berry GT, Elsas LJ 2nd, Levy HL, Segal S. Gibson JB, et al. Among authors: levy hl. Metabolism. 1995 May;44(5):597-604. doi: 10.1016/0026-0495(95)90116-7. Metabolism. 1995. PMID: 7752907

4

A new method of screening for inherited disorders of galactose metabolism.

Paigen K, Pacholec F, Levy HL. Paigen K, et al. Among authors: levy hl. J Lab Clin Med. 1982 Jun;99(6):895-907. J Lab Clin Med. 1982. PMID: 7042875

5

Comparison of amino acid concentrations between plasma and erythrocytes. Studies in normal human subjects and those with metabolic disorders.

Levy HL, Barkin E. Levy HL, et al. J Lab Clin Med. 1971 Oct;78(4):517-23. J Lab Clin Med. 1971. PMID: 5114049 No abstract available.

6

Family Genetic Risk Communication and Reverse Cascade Testing in the BabySeq Project.

Uveges MK, Smith HS, Pereira S, Genetti C, McGuire AL, Beggs AH, Green RC, Holm IA; BabySeq Project Team. Uveges MK, et al. Genet Med. 2024 Dec 24:101350. doi: 10.1016/j.gim.2024.101350. Online ahead of print. Genet Med. 2024. PMID: 39731470

7

Past as Prologue: Predicting Potential Psychosocial-Ethical Burdens of Positive Newborn Screens as Conditions Propagate.

Bush LW, Levy HL. Bush LW, et al. Among authors: levy hl. Int J Neonatal Screen. 2024 Feb 6;10(1):12. doi: 10.3390/ijns10010012. Int J Neonatal Screen. 2024. PMID: 38390976 Free PMC article.

8

The treatment of biochemical genetic diseases: From substrate reduction to nucleic acid therapies.

Vos EN, Demirbas D, Mangel M, Gozalbo MER, Levy HL, Berry GT. Vos EN, et al. Among authors: levy hl. Mol Genet Metab. 2023 Nov;140(3):107693. doi: 10.1016/j.ymgme.2023.107693. Epub 2023 Aug 30. Mol Genet Metab. 2023. PMID: 37716025 Review.

9

Classical phenylketonuria presenting as maternal PKU syndrome in the offspring of an intellectually normal woman.

Alghamdi MA, O'Donnell-Luria A, Almontashiri NA, AlAali WY, Ali HH, Levy HL. Alghamdi MA, et al. Among authors: levy hl. JIMD Rep. 2023 Jul 25;64(5):312-316. doi: 10.1002/jmd2.12384. eCollection 2023 Sep. JIMD Rep. 2023. PMID: 37701331 Free PMC article.

10

Is More Effective Newborn Screening for Homocystinuria on the Horizon?

Levy HL, Sahai I. Levy HL, et al. Clin Chem. 2023 Apr 28;69(5):433-434. doi: 10.1093/clinchem/hvad027. Clin Chem. 2023. PMID: 36949665 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

296 results

Search Page

Filters