Zhang Y - Search Results

1

[Analysis of the relationship between mitochondrial DNA deletion and clinical complexity of mitochondrial disease].

Zhang Y, Ma Y, Bu D, Liu H, Xia C, Zhang Y, Zhu S, Zheng X, Pei P, Wang S, Xu Y, Pan H, Qi Y. Zhang Y, et al. Zhonghua Yi Xue Za Zhi. 2015 Nov 10;95(42):3449-53. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26813137 Chinese.

2

Deletion of a 4977-bp Fragment in the Mitochondrial Genome Is Associated with Mitochondrial Disease Severity.

Zhang Y, Ma Y, Bu D, Liu H, Xia C, Zhang Y, Zhu S, Pan H, Pei P, Zheng X, Wang S, Xu Y, Qi Y. Zhang Y, et al. PLoS One. 2015 May 29;10(5):e0128624. doi: 10.1371/journal.pone.0128624. eCollection 2015. PLoS One. 2015. PMID: 26024530 Free PMC article. Clinical Trial.

3

[G14453A mutation in mitochondrial myopathy encephalomyopathy with lactic acidosis and stroke-like episodes].

Zheng X, Zhang Y, Zhang Y, Pei P, Ma Y. Zheng X, et al. Among authors: zhang y. Zhonghua Yi Xue Za Zhi. 2015 Aug 25;95(32):2623-5. Zhonghua Yi Xue Za Zhi. 2015. PMID: 26711613 Chinese.

4

Clinical and Molecular Characteristics in 100 Chinese Pediatric Patients with m.3243A>G Mutation in Mitochondrial DNA.

Xia CY, Liu Y, Liu H, Zhang YC, Ma YN, Qi Y. Xia CY, et al. Among authors: zhang yc. Chin Med J (Engl). 2016 Aug 20;129(16):1945-9. doi: 10.4103/0366-6999.187845. Chin Med J (Engl). 2016. PMID: 27503020 Free PMC article.

5

Delayed diagnosis of critical congenital heart defects predicting risk factors and survival rate in newborns in Beijing: a retrospective study.

Zhang W, Xu HY, Zhang YC, Liu KB. Zhang W, et al. J Int Med Res. 2021 Jul;49(7):3000605211028028. doi: 10.1177/03000605211028028. J Int Med Res. 2021. PMID: 34264137 Free PMC article.

6

Epidemiological Aspects, Prenatal Screening and Diagnosis of Congenital Heart Defects in Beijing.

Zhang Y, Zhang W, Xu H, Liu K. Zhang Y, et al. Among authors: zhang w. Front Cardiovasc Med. 2021 Dec 20;8:777899. doi: 10.3389/fcvm.2021.777899. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34988127 Free PMC article.

7

Non-invasive prenatal testing for the detection of trisomy 13, 18, and 21 and sex chromosome aneuploidies in 68,763 cases.

Zhang Y, Xu H, Zhang W, Liu K. Zhang Y, et al. Among authors: zhang w. Front Genet. 2022 Sep 15;13:864076. doi: 10.3389/fgene.2022.864076. eCollection 2022. Front Genet. 2022. PMID: 36186462 Free PMC article.

8

[Study on the clinical use of alpha-fetoprotein (AFP) colloidal gold diagnostic strip].

Jiang XM, Kong J, Lin T, Yu XY, Chen Y, Dai Y, Yang HY, Sun XL, Yang J, Yang YQ, Zhang YC. Jiang XM, et al. Among authors: zhang yc. Zhonghua Liu Xing Bing Xue Za Zhi. 2003 Mar;24(3):210-2. Zhonghua Liu Xing Bing Xue Za Zhi. 2003. PMID: 12816714 Chinese.

9

Systematic Review and Meta-Analysis of Factors Influencing Self-Medication in Children.

Bi B, Qin J, Zhang L, Lin C, Li S, Zhang Y. Bi B, et al. Among authors: zhang l, zhang y. Inquiry. 2023 Jan-Dec;60:469580231159744. doi: 10.1177/00469580231159744. Inquiry. 2023. PMID: 36998210 Free PMC article. Review.

10

Mendelian Randomization Study Reveals Causal Pathways for Hypertrophic Cardiomyopathy, Cardiovascular Proteins, and Atrial Fibrillation.

Zhang Y, Guo C, Wang L, Wu L, Lv J, Huang X, Yang W. Zhang Y, et al. Br J Hosp Med (Lond). 2025 Jan 24;86(1):1-19. doi: 10.12968/hmed.2024.0504. Epub 2025 Jan 14. Br J Hosp Med (Lond). 2025. PMID: 39862032

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