Du YL - Search Results

1

Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review.

Long ZB, Wang YW, Yang C, Liu G, Du YL, Nie GJ, Chang YZ, Han B. Long ZB, et al. Among authors: du yl. J Zhejiang Univ Sci B. 2016 Oct.;17(10):813-820. doi: 10.1631/jzus.B1600085. J Zhejiang Univ Sci B. 2016. PMID: 27704751 Free PMC article. Review.

2

A Hexagonal Perovskite Intergrowth Compound: La(2)Ca(2)MnO(7) We are thankful for financial support from the Youth Scientist Excellency Foundation (29625101), NSFC (29731010), and State Key Basic Research Program. Work performed at Argonne is supported by US DOE-BES under Contract No. W-31-109-ENG-38.

Wang Y, Lin J, Du Y, Qin R, Han B, Loong CK. Wang Y, et al. Angew Chem Int Ed Engl. 2000 Aug 4;39(15):2730-2732. doi: 10.1002/1521-3773(20000804)39:15<2730::aid-anie2730>3.0.co;2-l. Angew Chem Int Ed Engl. 2000. PMID: 10934408 No abstract available.

3

[MRI monitoring in diagnosis and follow-up of iron overload].

Zhang Q, Hou B, Wang L, Du Y, Han B, Feng F. Zhang Q, et al. Zhonghua Xue Ye Xue Za Zhi. 2015 Apr;36(4):302-6. doi: 10.3760/cma.j.issn.0253-2727.2015.04.009. Zhonghua Xue Ye Xue Za Zhi. 2015. PMID: 25916291 Free PMC article. Chinese.

4

A comparative analysis of clinical characteristics of patients with paroxysmal nocturnal hemoglobinuria between Asia and Europe/America.

Yu F, Du Y, Han B. Yu F, et al. Int J Hematol. 2016 Jun;103(6):649-54. doi: 10.1007/s12185-016-1995-1. Epub 2016 Apr 8. Int J Hematol. 2016. PMID: 27059871

5

[The preliminary research in paroxysmal nocturnal hemoglobinuria with thrombosis].

Du Y, Long Z, Xie H, Zhuang J, Han B. Du Y, et al. Zhonghua Xue Ye Xue Za Zhi. 2016 Apr;37(4):318-23. doi: 10.3760/cma.j.issn.0253-2727.2016.04.014. Zhonghua Xue Ye Xue Za Zhi. 2016. PMID: 27093996 Free PMC article. Chinese.

6

Genetic variants of C5 and polymorphisms of C3 in Chinese patients with paroxysmal nocturnal hemoglobinuria.

Du Y, Zhang Q, Han B. Du Y, et al. Int J Lab Hematol. 2016 Aug;38(4):e84-5. doi: 10.1111/ijlh.12512. Epub 2016 Jun 16. Int J Lab Hematol. 2016. PMID: 27307199 No abstract available.

7

Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis.

Wang Y, Du Y, Liu G, Guo S, Hou B, Jiang X, Han B, Chang Y, Nie G. Wang Y, et al. Int J Hematol. 2017 Apr;105(4):521-525. doi: 10.1007/s12185-016-2150-8. Epub 2016 Nov 28. Int J Hematol. 2017. PMID: 27896572

8

[Advances in genes mutation and pathophysiology of congenital sideroblastic anemia].

Long ZB, Du YL, Han B. Long ZB, et al. Among authors: du yl. Zhonghua Xue Ye Xue Za Zhi. 2016 Dec 14;37(12):1090-1093. doi: 10.3760/cma.j.issn.0253-2727.2016.12.018. Zhonghua Xue Ye Xue Za Zhi. 2016. PMID: 28088978 Free PMC article. Chinese. No abstract available.

9

[Research progress on clonal acquired sideroblastic anemia].

Long ZB, Du YL, Han B. Long ZB, et al. Among authors: du yl. Zhonghua Xue Ye Xue Za Zhi. 2017 Jan 14;38(1):83-86. doi: 10.3760/cma.j.issn.0253-2727.2017.01.021. Zhonghua Xue Ye Xue Za Zhi. 2017. PMID: 28219236 Free PMC article. Chinese. No abstract available.

10

Evaluation of the Efficiency of the Reticulocyte Hemoglobin Content on Diagnosis for Iron Deficiency Anemia in Chinese Adults.

Cai J, Wu M, Ren J, Du Y, Long Z, Li G, Han B, Yang L. Cai J, et al. Nutrients. 2017 May 2;9(5):450. doi: 10.3390/nu9050450. Nutrients. 2017. PMID: 28468320 Free PMC article.

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