Levy H - Search Results

1

Recommendations for evaluation of responsiveness to tetrahydrobiopterin (BH(4)) in phenylketonuria and its use in treatment.

Levy H, Burton B, Cederbaum S, Scriver C. Levy H, et al. Mol Genet Metab. 2007 Dec;92(4):287-91. doi: 10.1016/j.ymgme.2007.09.017. Mol Genet Metab. 2007. PMID: 18036498

2

Phenylketonuria: old disease, new approach to treatment.

Levy HL. Levy HL. Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):1811-3. doi: 10.1073/pnas.96.5.1811. Proc Natl Acad Sci U S A. 1999. PMID: 10051548 Free PMC article. Review. No abstract available.

3

Maternal phenylketonuria: an international study.

Koch R, Hanley W, Levy H, Matalon R, Rouse B, Trefz F, Guttler F, Azen C, Friedman E, Platt L, de la Cruz F. Koch R, et al. Among authors: levy h. Mol Genet Metab. 2000 Sep-Oct;71(1-2):233-9. doi: 10.1006/mgme.2000.3038. Mol Genet Metab. 2000. PMID: 11001815 Review.

4

The International Collaborative Study of Maternal Phenylketonuria: status report 1998.

Koch R, Friedman E, Azen C, Hanley W, Levy H, Matalon R, Rouse B, Trefz F, Waisbren S, Michals-Matalon K, Acosta P, Güttler F, Ullrich K, Platt L, de la Cruz F. Koch R, et al. Among authors: levy h. Eur J Pediatr. 2000 Oct;159 Suppl 2:S156-60. doi: 10.1007/pl00014383. Eur J Pediatr. 2000. PMID: 11043164

5

Arginase deficiency with lethal neonatal expression: evidence for the glutamine hypothesis of cerebral edema.

Picker JD, Puga AC, Levy HL, Marsden D, Shih VE, Degirolami U, Ligon KL, Cederbaum SD, Kern RM, Cox GF. Picker JD, et al. J Pediatr. 2003 Mar;142(3):349-52. doi: 10.1067/mpd.2003.97. J Pediatr. 2003. PMID: 12640389

6

The Maternal Phenylketonuria International Study: 1984-2002.

Koch R, Hanley W, Levy H, Matalon K, Matalon R, Rouse B, Trefz F, Güttler F, Azen C, Platt L, Waisbren S, Widaman K, Ning J, Friedman EG, de la Cruz F. Koch R, et al. Among authors: levy h. Pediatrics. 2003 Dec;112(6 Pt 2):1523-9. Pediatrics. 2003. PMID: 14654658 Clinical Trial.

7

The Resource Mothers Study of Maternal Phenylketonuria: preliminary findings.

Rohr F, Munier A, Sullivan D, Bailey I, Gennaccaro M, Levy H, Brereton H, Gleason S, Goss B, Lesperance E, Moseley K, Singh R, Tonyes L, Vespa H, Waisbren S. Rohr F, et al. Among authors: levy h. J Inherit Metab Dis. 2004;27(2):145-55. doi: 10.1023/B:BOLI.0000028785.20901.d9. J Inherit Metab Dis. 2004. PMID: 15159645 Clinical Trial.

8

The use of betaine in the treatment of elevated homocysteine.

Lawson-Yuen A, Levy HL. Lawson-Yuen A, et al. Mol Genet Metab. 2006 Jul;88(3):201-7. doi: 10.1016/j.ymgme.2006.02.004. Epub 2006 Mar 20. Mol Genet Metab. 2006. PMID: 16545978 Review.

9

Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12.

Smith SE, Kinney HC, Swoboda KJ, Levy HL. Smith SE, et al. Mol Genet Metab. 2006 Jun;88(2):138-45. doi: 10.1016/j.ymgme.2006.02.007. Epub 2006 Mar 30. Mol Genet Metab. 2006. PMID: 16574454

10

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.

Dobrowolski SF, Ellingson C, Coyne T, Grey J, Martin R, Naylor EW, Koch R, Levy HL. Dobrowolski SF, et al. Mol Genet Metab. 2007 Jul;91(3):218-27. doi: 10.1016/j.ymgme.2007.03.010. Epub 2007 May 14. Mol Genet Metab. 2007. PMID: 17502162

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