Qiu WJ - Search Results

1

Patients with progressive pseudorheumatoid dysplasia: from clinical diagnosis to molecular studies.

Ye J, Zhang HW, Qiu WJ, Han LS, Zhang YF, Gong ZW, Gu XF. Ye J, et al. Among authors: qiu wj. Mol Med Rep. 2012 Jan;5(1):190-5. doi: 10.3892/mmr.2011.619. Epub 2011 Oct 11. Mol Med Rep. 2012. PMID: 21993478

2

[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.

3

[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. Among authors: qiu wj. Zhonghua Er Ke Za Zhi. 2004 Jun;42(6):401-4. Zhonghua Er Ke Za Zhi. 2004. PMID: 15265419 Chinese.

4

[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.

5

[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. Among authors: qiu wj. Zhonghua Er Ke Za Zhi. 2004 Nov;42(11):865-6. Zhonghua Er Ke Za Zhi. 2004. PMID: 15631722 Chinese. No abstract available.

6

[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.

7

[Application of tandem mass spectrometry in diagnosis of organic acidemias].

Han LS, Gao XL, Ye J, Qiu WJ, Gu XF. Han LS, et al. Among authors: qiu wj. Zhonghua Er Ke Za Zhi. 2005 May;43(5):325-30. Zhonghua Er Ke Za Zhi. 2005. PMID: 15924743 Chinese.

8

[Screening and diagnosis of tetrahydrobiopterin responsive phenylalanine hydroxylase deficiency with tetrahydrobiopterin loading test].

Zhang ZX, Ye J, Qiu WJ, Han LS, Gu XF. Zhang ZX, et al. Among authors: qiu wj. Zhonghua Er Ke Za Zhi. 2005 May;43(5):335-9. Zhonghua Er Ke Za Zhi. 2005. PMID: 15924746 Chinese.

9

[Tetrahydrobiopterin loading test in differential diagnosis among hyperphenylalaninemia patients].

Zhang ZX, Ye J, Qiu WJ, Han LS, Gu XF. Zhang ZX, et al. Among authors: qiu wj. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):438-40. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16086286 Chinese.

10

[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: qiu wj. 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.

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