Lin Y - Search Results

1

C4OH is a potential newborn screening marker-a multicenter retrospective study of patients with beta-ketothiolase deficiency in China.

Lin Y, Yang Z, Yang C, Hu H, He H, Niu T, Liu M, Wang D, Sun Y, Shen Y, Li X, Yan H, Kong Y, Huang X. Lin Y, et al. Orphanet J Rare Dis. 2021 May 17;16(1):224. doi: 10.1186/s13023-021-01859-5. Orphanet J Rare Dis. 2021. PMID: 34001203 Free PMC article.

2

Clinical, biochemical and genetic analysis of Chinese patients with isobutyryl-CoA dehydrogenase deficiency.

Lin Y, Peng W, Jiang M, Lin C, Lin W, Zheng Z, Li M, Fu Q. Lin Y, et al. Among authors: lin c, lin w. Clin Chim Acta. 2018 Dec;487:133-138. doi: 10.1016/j.cca.2018.09.033. Epub 2018 Sep 22. Clin Chim Acta. 2018. PMID: 30253142

3

Combining newborn metabolic and genetic screening for neonatal intrahepatic cholestasis caused by citrin deficiency.

Lin Y, Liu Y, Zhu L, Le K, Shen Y, Yang C, Chen X, Hu H, Ma Q, Shi X, Hu Z, Yang J, Shen Y, Lin CH, Huang C, Huang X. Lin Y, et al. Among authors: lin ch. J Inherit Metab Dis. 2020 May;43(3):467-477. doi: 10.1002/jimd.12206. Epub 2019 Dec 29. J Inherit Metab Dis. 2020. PMID: 31845334

4

Newborn Screening for Spinal Muscular Atrophy in China Using DNA Mass Spectrometry.

Lin Y, Lin CH, Yin X, Zhu L, Yang J, Shen Y, Yang C, Chen X, Hu H, Ma Q, Shi X, Shen Y, Hu Z, Huang C, Huang X. Lin Y, et al. Among authors: lin ch. Front Genet. 2019 Dec 17;10:1255. doi: 10.3389/fgene.2019.01255. eCollection 2019. Front Genet. 2019. PMID: 31921298 Free PMC article.

5

[Newborn screening and variant analysis for methionine adenosyltransferase I/III deficiency].

Lin C, Zheng Q, Jiang M, Lin Y. Lin C, et al. Among authors: lin y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 May 10;37(5):527-531. doi: 10.3760/cma.j.issn.1003-9406.2020.05.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32335878 Chinese.

6

Screening 3.4 million newborns for primary carnitine deficiency in Zhejiang Province, China.

Lin Y, Xu H, Zhou D, Hu Z, Zhang C, Hu L, Zhang Y, Zhu L, Lu B, Zhang T, Huang X. Lin Y, et al. Clin Chim Acta. 2020 Aug;507:199-204. doi: 10.1016/j.cca.2020.04.039. Epub 2020 May 1. Clin Chim Acta. 2020. PMID: 32371215

7

Newborn screening for isovaleric acidemia in Quanzhou, China.

Lin Y, Chen D, Peng W, Wang K, Lin W, Zhuang J, Zheng Z, Li M, Fu Q. Lin Y, et al. Among authors: lin w. Clin Chim Acta. 2020 Oct;509:25-29. doi: 10.1016/j.cca.2020.06.010. Epub 2020 Jun 4. Clin Chim Acta. 2020. PMID: 32505769

8

Determination of methylmalonic acid, 2-methylcitric acid, and total homocysteine in dried blood spots by liquid chromatography-tandem mass spectrometry: A reliable follow-up method for propionylcarnitine-related disorders in newborn screening.

Hu Z, Yang J, Lin Y, Wang J, Hu L, Zhang C, Zhang Y, Huang X. Hu Z, et al. Among authors: lin y. J Med Screen. 2021 Jun;28(2):93-99. doi: 10.1177/0969141320937725. Epub 2020 Jul 2. J Med Screen. 2021. PMID: 32615850

9

Newborn screening and genetic characteristics of patients with short- and very long-chain acyl-CoA dehydrogenase deficiencies.

Lin Y, Zhang W, Chen D, Lin C, Zheng Z, Fu Q, Li M, Peng W. Lin Y, et al. Among authors: lin c. Clin Chim Acta. 2020 Nov;510:285-290. doi: 10.1016/j.cca.2020.07.038. Epub 2020 Jul 22. Clin Chim Acta. 2020. PMID: 32710939

10

Newborn screening for primary carnitine deficiency in Quanzhou, China.

Lin W, Wang K, Zheng Z, Chen Y, Fu C, Lin Y, Chen D. Lin W, et al. Among authors: lin y. Clin Chim Acta. 2021 Jan;512:166-171. doi: 10.1016/j.cca.2020.11.005. Epub 2020 Nov 9. Clin Chim Acta. 2021. PMID: 33181153

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

48,947 results

Search Page