Ye J - Search Results

1

Phenotype and genotype variation in primary carnitine deficiency.

Wang Y, Korman SH, Ye J, Gargus JJ, Gutman A, Taroni F, Garavaglia B, Longo N. Wang Y, et al. Among authors: ye j. Genet Med. 2001 Nov-Dec;3(6):387-92. doi: 10.1097/00125817-200111000-00002. Genet Med. 2001. PMID: 11715001 Free article.

2

Mutations in the organic cation/carnitine transporter OCTN2 in primary carnitine deficiency.

Wang Y, Ye J, Ganapathy V, Longo N. Wang Y, et al. Among authors: ye j. Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2356-60. doi: 10.1073/pnas.96.5.2356. Proc Natl Acad Sci U S A. 1999. PMID: 10051646 Free PMC article.

3

[Clinical features and gene analysis of TBC1D24 gene mutation related early-onset focal myoclonic epilepsy].

Leng XR, Ye J, Zhou QL, Qi XH, Dong YH, Zhang LP, Zhang YF, Wang YP, Li LP, Lin YC. Leng XR, et al. Among authors: ye j. Zhonghua Yi Xue Za Zhi. 2018 Feb 6;98(6):445-449. doi: 10.3760/cma.j.issn.0376-2491.2018.06.010. Zhonghua Yi Xue Za Zhi. 2018. PMID: 29429257 Chinese.

4

Large-scale study of clinical and biochemical characteristics of Chinese patients diagnosed with Krabbe disease.

Zhao S, Zhan X, Wang Y, Ye J, Han L, Qiu W, Gao X, Gu X, Zhang H. Zhao S, et al. Among authors: ye j. Clin Genet. 2018 Feb;93(2):248-254. doi: 10.1111/cge.13071. Epub 2017 Oct 17. Clin Genet. 2018. PMID: 28598007

5

[Clinical features and gene mutations of 6 patients with carnitine palmitoyltransferase 1A deficiency].

Yu Y, Shen LH, Qiu WJ, Zhang HW, Ye J, Liang LL, Wang Y, Ji WJ, Gu XF, Han LS. Yu Y, et al. Among authors: ye j. Zhonghua Yi Xue Za Zhi. 2021 Apr 13;101(14):1041-1044. doi: 10.3760/cma.j.cn112137-20200724-02206. Zhonghua Yi Xue Za Zhi. 2021. PMID: 33845545 Chinese.

6

Diagnosis, treatment, follow-up and gene mutation analysis in four Chinese children with biotinidase deficiency.

Ye J, Wang T, Han LS, Qiu WJ, Zhang HW, Zhang YF, Gao XL, Wang Y, Gu XF. Ye J, et al. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S295-302. doi: 10.1007/s10545-009-1238-1. Epub 2009 Aug 29. J Inherit Metab Dis. 2009. PMID: 19728141

7

[Applying multiplex ligation-dependent probe amplification in the diagnosis of 5 cases with ornithine transcarbamylase deficiency].

Gong ZW, Han LS, Ye J, Qiu WJ, Zhang HW, Yu YG, Liang LL, Gao XL, Wang Y, Ji WJ, Gu XF. Gong ZW, et al. Among authors: ye j. Zhonghua Er Ke Za Zhi. 2016 Jun 2;54(6):437-40. doi: 10.3760/cma.j.issn.0578-1310.2016.06.010. Zhonghua Er Ke Za Zhi. 2016. PMID: 27256231 Chinese.

8

[Analysis of gene mutation and clinical characteristics in patients with idiopathic epilepsy].

Sun HC, Wang CD, Li MY, Li LP, Zhao XL, Wang YP, Ye J. Sun HC, et al. Among authors: ye j. Zhonghua Yi Xue Za Zhi. 2017 Aug 15;97(31):2439-2442. doi: 10.3760/cma.j.issn.0376-2491.2017.31.011. Zhonghua Yi Xue Za Zhi. 2017. PMID: 28835045 Chinese.

9

Selective screening for inborn errors of metabolism on clinical patients using tandem mass spectrometry in China: a four-year report.

Han LS, Ye J, Qiu WJ, Gao XL, Wang Y, Gu XF. Han LS, et al. Among authors: ye j. J Inherit Metab Dis. 2007 Aug;30(4):507-14. doi: 10.1007/s10545-007-0543-9. Epub 2007 Mar 8. J Inherit Metab Dis. 2007. PMID: 17347912

10

[Culture conditions of engineered strain of L-asparaginase and the recombinant plasmid stability].

Wang Y, Qian S, Ye J, Meng G, Zhang S. Wang Y, et al. Among authors: ye j. Wei Sheng Wu Xue Bao. 1999 Dec;39(6):546-50. Wei Sheng Wu Xue Bao. 1999. PMID: 12555561 Chinese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

13,955 results

Search Page

Filters