Sun C - Search Results

1

Shi Y, Miao S, Fu Y, Sun C, Wang H, Zhai X. Shi Y, et al. Among authors: sun c. BMJ Open Qual. 2024 Apr 25;13(2):e002669. doi: 10.1136/bmjoq-2023-002669. BMJ Open Qual. 2024. PMID: 38670556 Free PMC article.

2

Improvement of the functioning and efficiency of a Code Blue system after training in a children's hospital in China.

Shi Y, Liu G, Cao D, Lu G, Yuan L, Qian Y, Xu J, Sun C, Ge M, Lai L, Wang X, Lu Y, Huang G, Zhai X. Shi Y, et al. Among authors: sun c. Transl Pediatr. 2021 Feb;10(2):236-243. doi: 10.21037/tp-20-171. Transl Pediatr. 2021. PMID: 33708509 Free PMC article.

3

[Identification of a novel CHS1/LYST variant in a Chinese pedigree affected with Chediak-Higashi syndrome].

Meng J, Wang H, Qian X, Miao H, Zhu X, Yu Y, Le J, Gao S, Sun C, Qian M, Zhai X. Meng J, et al. Among authors: sun c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):441-444. doi: 10.3760/cma.j.issn.1003-9406.2020.04.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219832 Chinese.

4

Clinical features and risk factors for severe influenza in children: A study from multiple hospitals in Shanghai.

Shi Y, Chen W, Zeng M, Shen G, Sun C, Liu G, Gong H, Wang C, Ge M, Xu J, Wang L, Lu A, Lu G, Zhai X. Shi Y, et al. Among authors: sun c. Pediatr Neonatol. 2021 Jul;62(4):428-436. doi: 10.1016/j.pedneo.2021.05.002. Epub 2021 May 14. Pediatr Neonatol. 2021. PMID: 34103261 Free article.

5

Efficacy of Low-Dose rhGM-CSF Treatment in a Patient With Severe Congenital Neutropenia Due to CSF3R Deficiency: Case Report of a Novel Biallelic CSF3R Mutation and Literature Review.

Zhou J, Sun C, Huang H, Zhu Q, Wen F, Dong Y, Wang H. Zhou J, et al. Among authors: sun c. Front Pediatr. 2021 Oct 29;9:746159. doi: 10.3389/fped.2021.746159. eCollection 2021. Front Pediatr. 2021. PMID: 34778134 Free PMC article.

6

[Construction of plant expression vectors harboring a peptide antibiotic-apidaecin gene and resistance analysis of the transgenic tobacco].

Wang H, Sun C, Peng XX. Wang H, et al. Among authors: sun c. Sheng Wu Gong Cheng Xue Bao. 2001 Jul;17(4):423-7. Sheng Wu Gong Cheng Xue Bao. 2001. PMID: 11702701 Chinese.

7

Comprehensive analysis of clinical spectrum and genotype associations in Chinese and literature reported KBG syndrome.

Li Q, Sun C, Yang L, Lu W, Luo F. Li Q, et al. Among authors: sun c. Transl Pediatr. 2021 Apr;10(4):834-842. doi: 10.21037/tp-20-385. Transl Pediatr. 2021. PMID: 34012832 Free PMC article.

8

Genotype and phenotype correlation in a cohort of Chinese congenital hypothyroidism patients with DUOX2 mutations.

Zheng Z, Yang L, Sun C, Wu J, Luo F, Zhou W, Lu W. Zheng Z, et al. Among authors: sun c. Ann Transl Med. 2020 Dec;8(24):1649. doi: 10.21037/atm-20-7165. Ann Transl Med. 2020. PMID: 33490161 Free PMC article.

9

A novel single nucleotide polymorphism in the protein tyrosine phosphatase N22 gene (PTPN22) is associated with Type 1 diabetes in a Chinese population.

Pei Z, Chen X, Sun C, Du H, Wei H, Song W, Yang Y, Zhang M, Lu W, Cheng R, Luo F. Pei Z, et al. Among authors: sun c. Diabet Med. 2014 Feb;31(2):219-26. doi: 10.1111/dme.12331. Epub 2013 Oct 21. Diabet Med. 2014. PMID: 24117662

10

Corrigendum: Glycated Hemoglobin (HbA1c) Concentrations Among Children and Adolescents With Diabetes in Middle- and Low-Income Countries, 2010-2019: A Retrospective Chart Review and Systematic Review of Literature.

Chen X, Pei Z, Zhang M, Xu Z, Zhao Z, Lu W, Chen L, Luo F, Chen T, Sun C. Chen X, et al. Among authors: sun c. Front Endocrinol (Lausanne). 2021 Sep 20;12:714389. doi: 10.3389/fendo.2021.714389. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34603202 Free PMC article.

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