Lin MT - Search Results

1

Mutation analysis of 218 Chinese patients with Wilson disease revealed no correlation between the canine copper toxicosis gene MURR1 and Wilson disease.

Wu ZY, Zhao GX, Chen WJ, Wang N, Wan B, Lin MT, Murong SX, Yu L. Wu ZY, et al. Among authors: lin mt. J Mol Med (Berl). 2006 May;84(5):438-42. doi: 10.1007/s00109-005-0036-y. Epub 2006 Jan 28. J Mol Med (Berl). 2006. PMID: 16649058

2

Molecular diagnosis and prophylactic therapy for presymptomatic Chinese patients with Wilson disease.

Wu ZY, Lin MT, Murong SX, Wang N. Wu ZY, et al. Among authors: lin mt. Arch Neurol. 2003 May;60(5):737-41. doi: 10.1001/archneur.60.5.737. Arch Neurol. 2003. PMID: 12756138 Clinical Trial.

3

[Genotype-phenotype correlation of patients with wilson disease in Chinese population].

Wu ZY, Wang N, Lin MT, Fang L, Murong SX. Wu ZY, et al. Among authors: lin mt. Zhonghua Yi Xue Za Zhi. 2003 Feb 25;83(4):309-11. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12812649 Chinese.

4

[Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy].

Wang N, Wu ZY, Wang CD, Wang ZQ, Lin MT, Fang L, Murong SX. Wang N, et al. Among authors: lin mt. Zhonghua Yi Xue Za Zhi. 2003 Apr 25;83(8):650-3. Zhonghua Yi Xue Za Zhi. 2003. PMID: 12887821 Chinese.

5

[The quantitative analysis of protein particles of erythrocyte membrane from Duchenne muscular dystrophy patients and the gene carriers].

Hong ZL, Murong SX, Zhong XR, Lin MT, Cheng WL, Lin X, Wang N. Hong ZL, et al. Among authors: lin mt, lin x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Feb;21(1):68-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 14767914 Chinese.

6

[Study on EcoR I fragment polymorphism of the subtelomeric domains within 4q35 and 10q26 with pulsed field gel electrophoresis in the Chinese population].

Wu ZY, Wang ZQ, Wang N, Lin MT, Murong SX. Wu ZY, et al. Among authors: lin mt. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):552-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583980 Chinese.

7

Rapid diagnosis of spinal muscular atrophy using denaturing high-performance liquid chromatography.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-Rong SX. Chen WJ, et al. Among authors: lin mt. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Jun;22(3):291-3. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15952118

8

Quantitative studies on SMN1 gene and carrier testing of spinal muscular atrophy.

Chen WJ, Wu ZY, Wang N, Lin MT, Mu-rong SX. Chen WJ, et al. Among authors: lin mt. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Dec;22(6):559-602. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 16331551

9

[Clinical analysis of dopa-responsive dystonia and mutation analysis of the GCH I gene].

Xie H, Wu ZY, Wang N, Li ZW, Lin MT, Murong SX. Xie H, et al. Among authors: lin mt. Zhonghua Er Ke Za Zhi. 2006 Jul;44(7):492-5. Zhonghua Er Ke Za Zhi. 2006. PMID: 17044972 Chinese.

10

Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysis.

Chen WJ, Wu ZY, Lin MT, Su JF, Lin Y, Murong SX, Wang N. Chen WJ, et al. Among authors: lin mt, lin y. Arch Neurol. 2007 Feb;64(2):225-31. doi: 10.1001/archneur.64.2.225. Arch Neurol. 2007. PMID: 17296838

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