Tang H - Search Results

1

Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California.

Gallant NM, Leydiker K, Wilnai Y, Lee C, Lorey F, Feuchtbaum L, Tang H, Carter J, Enns GM, Packman S, Lin HJ, Wilcox WR, Cederbaum SD, Abdenur JE. Gallant NM, et al. Among authors: tang h. Mol Genet Metab. 2017 Nov;122(3):76-84. doi: 10.1016/j.ymgme.2017.06.015. Epub 2017 Jul 8. Mol Genet Metab. 2017. PMID: 28711408

2

Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California.

Gallant NM, Leydiker K, Tang H, Feuchtbaum L, Lorey F, Puckett R, Deignan JL, Neidich J, Dorrani N, Chang E, Barshop BA, Cederbaum SD, Abdenur JE, Wang RY. Gallant NM, et al. Among authors: tang h. Mol Genet Metab. 2012 May;106(1):55-61. doi: 10.1016/j.ymgme.2012.02.007. Epub 2012 Feb 9. Mol Genet Metab. 2012. PMID: 22424739

3

Postanalytical tools improve performance of newborn screening by tandem mass spectrometry.

Hall PL, Marquardt G, McHugh DM, Currier RJ, Tang H, Stoway SD, Rinaldo P. Hall PL, et al. Among authors: tang h. Genet Med. 2014 Dec;16(12):889-95. doi: 10.1038/gim.2014.62. Epub 2014 May 29. Genet Med. 2014. PMID: 24875301 Free PMC article.

4

Damaged goods?: an empirical cohort study of blood specimens collected 12 to 23 hours after birth in newborn screening in California.

Tang H, Feuchtbaum L, Neogi P, Ho T, Gaffney L, Currier RJ. Tang H, et al. Genet Med. 2016 Mar;18(3):259-64. doi: 10.1038/gim.2015.154. Epub 2015 Dec 10. Genet Med. 2016. PMID: 26656653 Free article.

5

A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage Disorders.

Sanders KA, Gavrilov DK, Oglesbee D, Raymond KM, Tortorelli S, Hopwood JJ, Lorey F, Majumdar R, Kroll CA, McDonald AM, Lacey JM, Turgeon CT, Tucker JN, Tang H, Currier R, Isaya G, Rinaldo P, Matern D. Sanders KA, et al. Among authors: tang h. Int J Neonatal Screen. 2020 Jun;6(2):44. doi: 10.3390/ijns6020044. Epub 2020 May 30. Int J Neonatal Screen. 2020. PMID: 32802993 Free PMC article.

6

The First Year Experience of Newborn Screening for Pompe Disease in California.

Tang H, Feuchtbaum L, Sciortino S, Matteson J, Mathur D, Bishop T, Olney RS. Tang H, et al. Int J Neonatal Screen. 2020 Feb 7;6(1):9. doi: 10.3390/ijns6010009. eCollection 2020 Mar. Int J Neonatal Screen. 2020. PMID: 33073007 Free PMC article.

7

[No title available]

[No authors listed] [No authors listed] PMID: 33561046

8

Adrenoleukodystrophy Newborn Screening in California Since 2016: Programmatic Outcomes and Follow-Up.

Matteson J, Sciortino S, Feuchtbaum L, Bishop T, Olney RS, Tang H. Matteson J, et al. Among authors: tang h. Int J Neonatal Screen. 2021 Apr 17;7(2):22. doi: 10.3390/ijns7020022. Int J Neonatal Screen. 2021. PMID: 33920672 Free PMC article.

9

California's experience with SMA newborn screening: A successful path to early intervention.

Matteson J, Wu CH, Mathur D, Tang H, Sciortino S, Feuchtbaum L, Bishop T, Sharma SC, Neogi P, Fitzgibbon I, Olney RS. Matteson J, et al. Among authors: tang h. J Neuromuscul Dis. 2022;9(6):777-785. doi: 10.3233/JND-221561. J Neuromuscul Dis. 2022. PMID: 36278357

10

First Three Years' Experience of Mucopolysaccharidosis Type-I Newborn Screening in California.

Fillman T, Matteson J, Tang H, Mathur D, Zahedi R, Sen I, Bishop T, Neogi P, Feuchtbaum L, Olney RS, Sciortino S. Fillman T, et al. Among authors: tang h. J Pediatr. 2023 Dec;263:113644. doi: 10.1016/j.jpeds.2023.113644. Epub 2023 Jul 28. J Pediatr. 2023. PMID: 37516270

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