Shen N - Search Results

1

[Genetic diagnosis of a case with primary ciliary dyskinesia type 29 by next generation sequencing].

Shen N, Meng C, Liu Y, Gai Z. Shen N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):225-228. doi: 10.3760/cma.j.issn.1003-9406.2019.03.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835351 Chinese.

2

Gut microbiota dysbiosis is associated with Henoch-Schönlein Purpura in children.

Wang X, Zhang L, Wang Y, Liu X, Zhang H, Liu Y, Shen N, Yang J, Gai Z. Wang X, et al. Among authors: shen n. Int Immunopharmacol. 2018 May;58:1-8. doi: 10.1016/j.intimp.2018.03.003. Epub 2018 Mar 8. Int Immunopharmacol. 2018. PMID: 29525681

3

Oral microbiota dysbiosis and its association with Henoch-Schönlein Purpura in children.

Chen B, Wang J, Wang Y, Zhang J, Zhao C, Shen N, Yang J, Gai Z, Zhang L. Chen B, et al. Among authors: shen n. Int Immunopharmacol. 2018 Dec;65:295-302. doi: 10.1016/j.intimp.2018.10.017. Epub 2018 Oct 17. Int Immunopharmacol. 2018. PMID: 30342346

4

[Genetic analysis of a child with 13q deletion syndrome featuring congenital heart disease].

Shen N, Gou R, Yu H, Gao X, Pang H, Liu Y, Gai Z. Shen N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):620-623. doi: 10.3760/cma.j.issn.1003-9406.2019.06.023. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055821 Chinese.

5

[Clinical and genetic analysis of a case carrying 7p22.3 deletion, 7p22.3p22.2 duplication and 7q33q36.3 duplication].

Shen N, Guo R, Liu Y, Gai Z. Shen N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jul 10;36(7):708-711. doi: 10.3760/cma.j.issn.1003-9406.2019.07.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31302917 Chinese.

6

[Analysis of RPS6KA3 gene mutation in a Chinese pedigree affected with Coffin-Lowry syndrome].

Shen N, Liu Y, Zhang K, Lyu Y, Gao M, Ma J, Xu L, Gai Z. Shen N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Aug 10;36(8):798-800. doi: 10.3760/cma.j.issn.1003-9406.2019.08.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31400131 Chinese.

7

[Variant analysis of CCBE1 gene in a case of Hennekam lymphangiectasia-lymphedema syndrome type 1].

Ren Y, Liu Y, Lyu Y, Gao M, Wang D, Wan Y, Ma J, Shen N, Gai Z. Ren Y, et al. Among authors: shen n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jun 10;37(6):669-672. doi: 10.3760/cma.j.issn.1003-9406.2020.06.018. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32472549 Chinese.

8

[A case of Neonatal generalized atrophic benign epidermolysis bullosa due to variants of COL17A1 gene].

Zhu S, Qiao J, Shen N, Zhou Y, Cen M, Jiang Y. Zhu S, et al. Among authors: shen n. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Jun 10;41(6):741-744. doi: 10.3760/cma.j.cn511374-20220207-00092. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024. PMID: 38818561 Chinese.

9

[Analysis of PDHA1 gene variant in a patient with pyruvate dehydrogenase E1alpha deficiency and pyramidal tract involvement].

Shen N, Wang H, Shi Y, Geng D, Qun S, Ge W. Shen N, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jun 10;37(6):657-660. doi: 10.3760/cma.j.issn.1003-9406.2020.06.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32472546 Chinese.

10

Association between history of viral infections and melanoma mortality.

Shen N, Creveling P, Horns JJ, Bleicher J, Hyngstrom J, Bowles T, Andreae M, Onega T, Asare EA. Shen N, et al. Heliyon. 2024 Nov 12;10(22):e40353. doi: 10.1016/j.heliyon.2024.e40353. eCollection 2024 Nov 30. Heliyon. 2024. PMID: 39619574 Free PMC article.

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