Qiu X - Search Results

1

Perinatal risk factors for congenital hypothyroidism: A retrospective cohort study performed at a tertiary hospital in China.

Zhou J, Luo J, Lin J, Zeng Y, Qiu X, Zhu W, Liu G. Zhou J, et al. Among authors: qiu x. Medicine (Baltimore). 2020 Jun 26;99(26):e20838. doi: 10.1097/MD.0000000000020838. Medicine (Baltimore). 2020. PMID: 32590776 Free PMC article.

2

Association between genetic polymorphism of heme oxygenase 1 promoter and neonatal hyperbilirubinemia: a meta-analysis.

Zhou JF, Luo JY, Zhu WB, Yang CY, Zeng YL, Qiu XL. Zhou JF, et al. J Matern Fetal Neonatal Med. 2021 Jan;34(1):12-23. doi: 10.1080/14767058.2019.1570115. Epub 2019 Jan 30. J Matern Fetal Neonatal Med. 2021. PMID: 30700176

3

A verification of the application of the non-derivatized mass spectrometry method in newborns screening of metabolic disorders.

Zheng Y, Chen Y, Qiu X, Chen W, Lin Q, Zeng Y, Zhao H, Zhu W. Zheng Y, et al. Among authors: qiu x. Medicine (Baltimore). 2019 May;98(19):e15500. doi: 10.1097/MD.0000000000015500. Medicine (Baltimore). 2019. PMID: 31083189 Free PMC article.

4

Gene spectrum and clinical traits of 10 patients with primary carnitine deficiency.

Chen Y, Lin Q, Zeng Y, Qiu X, Liu G, Zhu W. Chen Y, et al. Among authors: qiu x. Mol Genet Genomic Med. 2021 Feb;9(2):e1583. doi: 10.1002/mgg3.1583. Epub 2021 Feb 9. Mol Genet Genomic Med. 2021. PMID: 33560599 Free PMC article.

5

Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian.

Chen Y, Lin X, Lin Q, Zeng Y, Qiu X, Liu G, Zhu W. Chen Y, et al. Among authors: qiu x. Medicine (Baltimore). 2021 Mar 12;100(10):e24161. doi: 10.1097/MD.0000000000024161. Medicine (Baltimore). 2021. PMID: 33725819 Free PMC article.

6

Characterization of phenylalanine hydroxylase gene variants and analysis of genotype-phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China.

Zhou J, Zeng Y, Qiu X, Lin Q, Chen W, Luo J, Xu L. Zhou J, et al. Among authors: qiu x. Mol Biol Rep. 2022 Nov;49(11):10409-10419. doi: 10.1007/s11033-022-07579-8. Epub 2022 Sep 14. Mol Biol Rep. 2022. PMID: 36104584 Free PMC article.

7

Biochemical and molecular features of chinese patients with glutaric acidemia type 1 from Fujian Province, southeastern China.

Zhou J, Li G, Deng L, Zhao P, Zeng Y, Qiu X, Luo J, Xu L. Zhou J, et al. Among authors: qiu x. Orphanet J Rare Dis. 2023 Jul 26;18(1):215. doi: 10.1186/s13023-023-02833-z. Orphanet J Rare Dis. 2023. PMID: 37496092 Free PMC article.

8

Biochemical and molecular features of tetrahydrobiopterin deficiency in Fujian Province, southeastern China.

Qiu X, Zhao P, Luo J, Li G, Deng L, Zeng Y, Xu L, Zhou J. Qiu X, et al. Front Genet. 2023 Aug 11;14:1250568. doi: 10.3389/fgene.2023.1250568. eCollection 2023. Front Genet. 2023. PMID: 37636258 Free PMC article.

9

Newborn Screening of 6 Lysosomal Storage Disorders by Tandem Mass Spectrometry.

Chen Y, Yang Y, Zeng Y, Lin Q, Zhao P, Mao B, Qiu X, Huang T, Xu L, Zhu W. Chen Y, et al. Among authors: qiu x. Clin Pediatr (Phila). 2024 Oct;63(10):1364-1370. doi: 10.1177/00099228231219336. Epub 2023 Dec 22. Clin Pediatr (Phila). 2024. PMID: 38135922

10

Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis.

Zhou J, Li G, Zeng Y, Qiu X, Zhao P, Huang T, Wang X, Luo J, Lin N, Xu L. Zhou J, et al. Among authors: qiu x. Orphanet J Rare Dis. 2024 Jul 3;19(1):248. doi: 10.1186/s13023-024-03267-x. Orphanet J Rare Dis. 2024. PMID: 38961493 Free PMC article. Review.

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