Tang H - Search Results

1

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

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

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.

4

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

5

The role of exome sequencing in newborn screening for inborn errors of metabolism.

Adhikari AN, Gallagher RC, Wang Y, Currier RJ, Amatuni G, Bassaganyas L, Chen F, Kundu K, Kvale M, Mooney SD, Nussbaum RL, Randi SS, Sanford J, Shieh JT, Srinivasan R, Sunderam U, Tang H, Vaka D, Zou Y, Koenig BA, Kwok PY, Risch N, Puck JM, Brenner SE. Adhikari AN, et al. Among authors: tang h. Nat Med. 2020 Sep;26(9):1392-1397. doi: 10.1038/s41591-020-0966-5. Epub 2020 Aug 10. Nat Med. 2020. PMID: 32778825 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

The Clinical Impact of CLIR Tools toward Rapid Resolution of Post-Newborn Screening Confirmatory Testing for X-Linked Adrenoleukodystrophy in California.

Tang H, Matteson J, Rinaldo P, Tortorelli S, Currier R, Sciortino S. Tang H, et al. Int J Neonatal Screen. 2020 Aug 5;6(3):62. doi: 10.3390/ijns6030062. eCollection 2020 Sep. Int J Neonatal Screen. 2020. PMID: 33123639 Free PMC article.

8

[No title available]

[No authors listed] [No authors listed] PMID: 33239588

9

[No title available]

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

10

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.

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