Wen PQ - Search Results

1

[Analysis of clinical features and gene mutations in two Chinese pedigrees with late-onset methylmalonic acidemia, cblC type].

Cui D, Chen SL, Wen PQ, Hu YH, Chen XW, Shen D, Yuan Q, Song P, Liao JX, Li CR. Cui D, et al. Among authors: wen pq. Zhonghua Er Ke Za Zhi. 2010 Jun;48(6):469-72. Zhonghua Er Ke Za Zhi. 2010. PMID: 21055272 Chinese.

2

[Analysis of clinical features and GCDH gene mutations in four patients with glutaric academia type I].

Wen P-, Wang GB, Liu XH, Chen ZL, Shang Y, Cui D, Song P, Yuan Q, Chen SL, Liao JX, Li CR. Wen P-, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):642-7. doi: 10.3760/cma.j.issn.1003-9406.2012.06.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23225040 Chinese.

3

[Analysis of clinical phenotype and ACAT1 gene mutation in a family affected with beta-ketothiolase deficiency].

Wen P, Chen Z, Wang G, Su Z, Zhang X, Tang G, Cui D, Liu X, Li C. Wen P, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Jun;33(3):286-91. doi: 10.3760/cma.j.issn.1003-9406.2016.03.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27264805 Chinese.

4

[Clinical features and genetic analysis of a case with carnitine palmitoyltransferase 1A deficiency].

Cui D, Hu Y, Shen D, Tang G, Zhang M, Duan J, Wen P, Liao J, Ma D, Chen S. Cui D, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Apr 10;34(2):228-231. doi: 10.3760/cma.j.issn.1003-9406.2017.02.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28397225 Chinese.

5

[SLC25A13 gene analysis in neonates with intrahepatic cholestasis caused by citrin deficiency].

Wen PQ, Wang GB, Chen ZL, Cui D, Yuan Q, Song P, Chen SL, Liao JX, Li CR. Wen PQ, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Apr;13(4):303-8. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 21507300 Free article. Chinese.

6

[Clinical investigation and mutation analysis of a child with citrin deficiency complicated with purpura, convulsive seizures and methioninemia].

Wen PQ, Wang GB, Chen ZL, Liu XH, Cui D, Shang Y, Li CR. Wen PQ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Dec;30(6):649-53. doi: 10.3760/cma.j.issn.1003-9406.2013.06.003. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 24327139 Chinese.

7

[Utilization of high-resolution melting analysis to screen patients with neonatal intrahepatic cholestasis caused by citrin deficiency].

Wen PQ, Wang GB, Chen ZL, Cui D, Liu XH, Ying LF, Song P, Yuan Q, Chen SL, Liao JX. Wen PQ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Apr;29(2):167-71. doi: 10.3760/cma.j.issn.1003-9406.2012.02.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22487826 Chinese.

8

[Genetic analysis of ASS1, ASL and SLC25A13 in citrullinemia patients].

Wen P, Chen Z, Wang G, Liu X, Chen L, Chen S, Wan L, Cui D, Shang Y, Li C. Wen P, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Jun;31(3):268-71. doi: 10.3760/cma.j.issn.1003-9406.2014.03.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24927999 Chinese.

9

[Analysis of ornithine transcarbamylase gene mutations in three boys affected with late-onset ornithine transcarbamylase deficiency].

Chen Z, Wen P, Wang G, Liu X, Chen L, Chen S, Wan L, Cui D, Shang Y, Li C. Chen Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):565-9. doi: 10.3760/cma.j.issn.1003-9406.2014.01.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25297582 Chinese.

10

[Analysis of PCCA and PCCB gene mutations in patients with propionic acidemia].

Chen Z, Wen P, Wang G, Hu Y, Liu X, Chen L, Chen S, Wan L, Cui D, Shang Y, Li C. Chen Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):26-30. doi: 10.3760/cma.j.issn.1003-9406.2015.01.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 25636094 Chinese.

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