Zhou JD - Search Results

1

[Diagnosis, treatment and gene mutation analysis of the first case with dihydropteridine reductase deficiency in the mainland of China].

Ye J, Qiu WJ, Han LS, Zhang HW, Zhou JD, Gao XL, Wang Y, Gu XF. Ye J, et al. Among authors: zhou jd. Zhonghua Er Ke Za Zhi. 2008 Apr;46(4):281-5. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099731 Chinese.

2

[Screening for tetrahydrobiopterin metabolic disorders and related gene analysis among the patients with motor disturbance and mental retardation].

Ye J, Liu XQ, Qiu WJ, Han LS, Zhou JD, Zhang YF, Gu XF. Ye J, et al. Among authors: zhou jd. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Apr;24(2):210-2. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17407085 Chinese.

3

[Diagnosis, treatment and long-term following up of 223 patients with hyperphenylalaninemia detected by neonatal screening programs].

Ye J, Qiu WJ, Han LS, Zhang YJ, Zhou JD, Zhang YF, Wu YL, Gu XF. Ye J, et al. Among authors: zhou jd. Zhonghua Yu Fang Yi Xue Za Zhi. 2007 May;41(3):189-92. Zhonghua Yu Fang Yi Xue Za Zhi. 2007. PMID: 17708870 Chinese.

4

[The investigation of differential diagnostic development and incidence of tetrahydrobiopterin deficiency].

Ye J, Qiu WJ, Han LS, Zhou JD, Gao XL, Gu XF. Ye J, et al. Among authors: zhou jd. Zhonghua Yu Fang Yi Xue Za Zhi. 2009 Feb;43(2):128-31. Zhonghua Yu Fang Yi Xue Za Zhi. 2009. PMID: 19534905 Chinese.

5

[Application of enzyme assay and gene analysis in the prenatal diagnosis for a family with glycogen storage disease type II].

Zeng MH, Qiu WJ, Gu XF, Wang Y, Zhou JD, Ye J, Han LS, Zhang HW. Zeng MH, et al. Among authors: zhou jd. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Jun;28(3):261-5. doi: 10.3760/cma.j.issn.1003-9406.2011.03.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 21644219 Chinese.

6

QDPR gene mutation and clinical follow-up in Chinese patients with dihydropteridine reductase deficiency.

Lu DY, Ye J, Han LS, Qiu WJ, Zhang HW, Zhou JD, Bao PZ, Zhang YF, Gu XF. Lu DY, et al. Among authors: zhou jd. World J Pediatr. 2014 Aug;10(3):219-26. doi: 10.1007/s12519-014-0496-7. Epub 2014 Aug 15. World J Pediatr. 2014. PMID: 25124972

7

[Neonatal screening for congenital adrenal hyperplasia in Shanghai areas].

Gu X, Zhou J, Ye J. Gu X, et al. Zhonghua Yu Fang Yi Xue Za Zhi. 2002 Jan;36(1):16-8. Zhonghua Yu Fang Yi Xue Za Zhi. 2002. PMID: 11955341 Chinese.

8

A case of Ph⁺ acute lymphoblastic leukemia and EGFR mutant lung adenocarcinoma synchronous overlap: may one TKI drug solve two diseases?

Zhang Q, Zhou JD, Ding H, Yang L, Lu C, Chu MQ, Qian J, Zhang TJ. Zhang Q, et al. Among authors: zhou jd. BMC Med Genomics. 2024 Jul 8;17(1):182. doi: 10.1186/s12920-024-01955-y. BMC Med Genomics. 2024. PMID: 38978091 Free PMC article.

9

Response.

Zhang X, Tang D, Zhou JD, Li WJ, Wang L. Zhang X, et al. Among authors: zhou jd. Gastrointest Endosc. 2024 Mar;99(3):476-477. doi: 10.1016/j.gie.2023.10.052. Gastrointest Endosc. 2024. PMID: 38368048 No abstract available.

10

POU2F2-mediated upregulation of lncRNA PTPRG-AS1 inhibits ferroptosis in breast cancer via miR-376c-3p/SLC7A11 axis.

Li J, Li PT, Wu W, Ding BN, Wen YG, Cai HL, Liu SX, Hong T, Zhang JF, Zhou JD, Qian LY, Du J. Li J, et al. Among authors: zhou jd. Epigenomics. 2024 Feb;16(4):215-231. doi: 10.2217/epi-2023-0100. Epub 2024 Feb 6. Epigenomics. 2024. PMID: 38318853

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