Wei M - Search Results

1

Clinical features of gout in adult patients with type Ia glycogen storage disease: a single-centre retrospective study and a review of literature.

Xu N, Han X, Zhang Y, Huang X, Zhu W, Shen M, Zhang W, Jialin C, Wei M, Qiu Z, Zeng X. Xu N, et al. Among authors: wei m. Arthritis Res Ther. 2022 Feb 26;24(1):58. doi: 10.1186/s13075-021-02706-5. Arthritis Res Ther. 2022. PMID: 35219330 Free PMC article. Review.

2

Spectrum of AGL mutations in Chinese patients with glycogen storage disease type III: identification of 31 novel mutations.

Lu C, Qiu Z, Sun M, Wang W, Wei M, Zhang X. Lu C, et al. Among authors: wei m. J Hum Genet. 2016 Jul;61(7):641-5. doi: 10.1038/jhg.2016.24. Epub 2016 Mar 17. J Hum Genet. 2016. PMID: 26984562

3

[Heterogeneous phenotypes in Chinese glycogen storage disease type Ia patients with homozygous G727T mutation].

Qiu ZQ, Wei M, Liu G, Liu GY. Qiu ZQ, et al. Among authors: wei m. Zhonghua Er Ke Za Zhi. 2003 Apr;41(4):252-5. Zhonghua Er Ke Za Zhi. 2003. PMID: 14754525 Chinese.

4

[Mutation analysis of glycogen debrancher enzyme gene in five Chinese patients with glycogen storage disease type III].

Zhuang TF, Qiu ZQ, Wei M, Huang SZ. Zhuang TF, et al. Among authors: wei m. Zhonghua Er Ke Za Zhi. 2005 Feb;43(2):85-8. Zhonghua Er Ke Za Zhi. 2005. PMID: 15833157 Chinese.

5

A novel MAGED2 variant in a Chinese preterm newborn with transient antenatal Bartter's syndrome with 4 years follow-up.

Ma M, Zhang M, Zhou Y, Yao F, Wei M, Li Z, Qiu Z. Ma M, et al. Among authors: wei m. BMC Nephrol. 2021 Dec 11;22(1):408. doi: 10.1186/s12882-021-02553-1. BMC Nephrol. 2021. PMID: 34895150 Free PMC article.

6

Mutation Analysis of 16 Mucolipidosis II and III Alpha/Beta Chinese Children Revealed Genotype-Phenotype Correlations.

Liu S, Zhang W, Shi H, Yao F, Wei M, Qiu Z. Liu S, et al. Among authors: wei m. PLoS One. 2016 Sep 23;11(9):e0163204. doi: 10.1371/journal.pone.0163204. eCollection 2016. PLoS One. 2016. PMID: 27662472 Free PMC article.

7

[A Chinese girl with cleidocranial dysplasia (CCD) caused by the recurrent R190W mutation in RUNX 2].

Qiu ZQ, Tang AL, Yu W, Ao Y, Wilson HY, Wei M, Zhang X. Qiu ZQ, et al. Among authors: wei m. Zhonghua Er Ke Za Zhi. 2004 Oct;42(10):759-61. Zhonghua Er Ke Za Zhi. 2004. PMID: 16221346 Chinese.

8

[Clinical and molecular genetic study on two patients of the juvenile form of Pompe disease in China].

Qiu JJ, Wei M, Zhang WM, Shi HP. Qiu JJ, et al. Among authors: wei m. Zhonghua Er Ke Za Zhi. 2007 Oct;45(10):760-4. Zhonghua Er Ke Za Zhi. 2007. PMID: 18211760 Chinese.

9

Chromatin accessibility analysis reveals regulatory dynamics of developing human retina and hiPSC-derived retinal organoids.

Xie H, Zhang W, Zhang M, Akhtar T, Li Y, Yi W, Sun X, Zuo Z, Wei M, Fang X, Yao Z, Dong K, Zhong S, Liu Q, Shen Y, Wu Q, Wang X, Zhao H, Bao J, Qu K, Xue T. Xie H, et al. Among authors: wei m. Sci Adv. 2020 Feb 7;6(6):eaay5247. doi: 10.1126/sciadv.aay5247. eCollection 2020 Feb. Sci Adv. 2020. PMID: 32083182 Free PMC article.

10

[Clinical features and TTC21B genotype of a child with nephronophthisis type 12].

Jian S, Wei QJ, Liu YT, Wang W, Zhou Y, Quan MY, He YY, Song HM, Wei M. Jian S, et al. Among authors: wei m, wei qj. Zhongguo Dang Dai Er Ke Za Zhi. 2019 Jun;21(6):580-584. doi: 10.7499/j.issn.1008-8830.2019.06.015. Zhongguo Dang Dai Er Ke Za Zhi. 2019. PMID: 31208513 Free PMC article. Chinese.

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