Wu D - Search Results

1

[Studies on PANK2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome].

Zhang Y, Tang B, Guo J, Long Z, Xia K, Pan Q, Hu Z, Wu D, Tang J, Chen T, Yan X. Zhang Y, et al. Among authors: wu d. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):189-91. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793782 Chinese.

2

[The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7].

Yin XZ, Zhang BR, Wu DW, Tian J, Zhang H. Yin XZ, et al. Yi Chuan. 2007 Jun;29(6):688-92. doi: 10.1360/yc-007-0688. Yi Chuan. 2007. PMID: 17650485 Chinese.

3

[Methylation analysis of CpG island DNA of FMR1 gene in the fragile X syndrome].

Wu DW, Zhu ZW, Zhao ZY, Qu YP, Yang JB. Wu DW, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):60-3. doi: 10.3760/cma.j.issn.1003-9406.2013.01.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450481 Chinese.

4

Clinical features and Cu/Zn superoxide dismutase gene mutations in two mainland Chinese families with amyotrophic lateral sclerosis.

Zhao G, Yin X, Wu D, Mao S, Yin H, Zhang B. Zhao G, et al. Among authors: wu d. Int J Neurosci. 2011 Apr;121(4):191-5. doi: 10.3109/00207454.2010.542841. Int J Neurosci. 2011. PMID: 21329474

5

SLC34A2 Gene mutation of pulmonary alveolar microlithiasis: report of four cases and review of literatures.

Yin X, Wang H, Wu D, Zhao G, Shao J, Dai Y. Yin X, et al. Among authors: wu d. Respir Med. 2013 Feb;107(2):217-22. doi: 10.1016/j.rmed.2012.10.016. Epub 2012 Nov 17. Respir Med. 2013. PMID: 23164546 Free article. Review.

6

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Phenotypic and mutational spectrum in patients from mainland China.

Yin X, Wu D, Wan J, Yan S, Lou M, Zhao G, Zhang B. Yin X, et al. Among authors: wu d. Int J Neurosci. 2015;125(8):585-92. doi: 10.3109/00207454.2014.951929. Epub 2014 Sep 1. Int J Neurosci. 2015. PMID: 25105908

7

A novel TFG c.793C>G mutation in a Chinese pedigree with Charcot-Marie-Tooth disease 2.

Wu DW, Li Y, Yin X, Zhang B. Wu DW, et al. Brain Behav. 2020 Sep;10(9):e01724. doi: 10.1002/brb3.1724. Epub 2020 Jul 14. Brain Behav. 2020. PMID: 32666699 Free PMC article.

8

[Clinical and genetic analysis of a pedigree of Kennedy disease].

Ou-Yang ZY, Song SJ, Liu JR, Zhang BR, Wu DW. Ou-Yang ZY, et al. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2011 Sep;40(5):555-8. doi: 10.3785/j.issn.1008-9292.2011.05.016. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2011. PMID: 21984161 Chinese.

9

Novel human pathological mutations. SLC34A2. Disease: pulmonary alveolar microlithiasis.

Wang H, Yin X, Wu D. Wang H, et al. Among authors: wu d. Hum Genet. 2010 Apr;127(4):471. doi: 10.1007/s00439-010-0870-z. Hum Genet. 2010. PMID: 21488279 No abstract available.

10

[Polymicrogyria associated with ADGRG1 gene variations in a child].

Liu XR, Jiang TJ, Yang XH, Wu DW, Tong F, Gao F. Liu XR, et al. Among authors: wu dw. Zhonghua Er Ke Za Zhi. 2024 Nov 2;62(11):1110-1112. doi: 10.3760/cma.j.cn112140-20240621-00420. Zhonghua Er Ke Za Zhi. 2024. PMID: 39429086 Chinese.

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