Gu X - Search Results

1

Identification of a distinct mutation spectrum in the SMPD1 gene of Chinese patients with acid sphingomyelinase-deficient Niemann-Pick disease.

Zhang H, Wang Y, Gong Z, Li X, Qiu W, Han L, Ye J, Gu X. Zhang H, et al. Among authors: gu x. Orphanet J Rare Dis. 2013 Jan 28;8:15. doi: 10.1186/1750-1172-8-15. Orphanet J Rare Dis. 2013. PMID: 23356216 Free PMC article.

2

Screening for tetrahydrobiopterin deficiency among hyperphenylalaninemia patients in Southern China.

Ye J, Liu X, Ma X, Zhang Y, Huang X, Chen R, Gu X. Ye J, et al. Among authors: gu x. Chin Med J (Engl). 2002 Feb;115(2):217-21. Chin Med J (Engl). 2002. PMID: 11940335

3

[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.

4

[Alteration of gene expression profiles of cultured embryo rat cortex induced by phenylalanine].

Zhang HW, Gu XF. Zhang HW, et al. Sheng Li Xue Bao. 2004 Apr 25;56(2):183-91. Sheng Li Xue Bao. 2004. PMID: 15127128 Free article. Chinese.

5

[Study on mutations of exon 12 of the PAH gene in 127 phenylketonuria patients].

Qiu WJ, Zhang YF, Ye J, Han LS, Gu XF. Qiu WJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):261-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15192831 Chinese.

6

[A pilot study of selective screening for high risk children with inborn error of metabolism using tandem mass spectrometry in China].

Gu XF, Han LS, Gao XL, Yan YL, Ye J, Qiu WJ. Gu XF, et al. Zhonghua Er Ke Za Zhi. 2004 Jun;42(6):401-4. Zhonghua Er Ke Za Zhi. 2004. PMID: 15265419 Chinese.

7

[Molecular genetic analysis of congenital lipoid adrenal hyperplasia].

Qiu WJ, Ye J, Han B, Han LS, Gu XF. Qiu WJ, et al. Zhonghua Er Ke Za Zhi. 2004 Aug;42(8):585-8. Zhonghua Er Ke Za Zhi. 2004. PMID: 15347444 Chinese.

8

[A discussion on risk factors of final height in 21-hydroxylase deficiency patients].

Han B, Han LS, Ye J, Qiu WJ, Gu XF. Han B, et al. Zhonghua Er Ke Za Zhi. 2004 Nov;42(11):865-6. Zhonghua Er Ke Za Zhi. 2004. PMID: 15631722 Chinese. No abstract available.

9

[Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis].

Qiu WJ, Zhang YF, Pan J, Ye J, Liu XQ, Han LS, Gu XF. Qiu WJ, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Feb;22(1):44-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15696478 Chinese.

10

[Effect of phenylalanine on genes expression of Rho GTPases: possible relevance to neuron damage induced by phenylalanine].

Zhang YJ, Zhang HW, Gu XF. Zhang YJ, et al. Zhonghua Er Ke Za Zhi. 2005 Mar;43(3):210-1. Zhonghua Er Ke Za Zhi. 2005. PMID: 15833199 Chinese. No abstract available.

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