Wei YH - Search Results

1

Leber's hereditary optic neuropathy--the spectrum of mitochondrial DNA mutations in Chinese patients.

Yen MY, Wang AG, Chang WL, Hsu WM, Liu JH, Wei YH. Yen MY, et al. Among authors: wei yh. Jpn J Ophthalmol. 2002 Jan-Feb;46(1):45-51. doi: 10.1016/s0021-5155(01)00460-9. Jpn J Ophthalmol. 2002. PMID: 11853713

2

Specific restriction fragment length polymorphism in liver mitochondrial DNA of the Chinese.

Yen TC, Hsu JH, Lee SC, Lee JF, Wei YH. Yen TC, et al. Among authors: wei yh. Zhonghua Yi Xue Za Zhi (Taipei). 1992 Sep;50(3):177-83. Zhonghua Yi Xue Za Zhi (Taipei). 1992. PMID: 1358420

3

Mitochondrial DNA alterations as ageing-associated molecular events.

Wei YH. Wei YH. Mutat Res. 1992 Sep;275(3-6):145-55. doi: 10.1016/0921-8734(92)90019-l. Mutat Res. 1992. PMID: 1383757 Review.

4

Age-dependent 6kb deletion in human liver mitochondrial DNA.

Yen TC, Pang CY, Hsieh RH, Su CH, King KL, Wei YH. Yen TC, et al. Among authors: wei yh. Biochem Int. 1992 Mar;26(3):457-68. Biochem Int. 1992. PMID: 1627156

5

Mitochondrial DNA mutation in Leber's hereditary optic neuropathy.

Yen MY, Yen TC, Pang CY, Liu JH, Wei YH. Yen MY, et al. Among authors: wei yh. Invest Ophthalmol Vis Sci. 1992 Jul;33(8):2561-6. Invest Ophthalmol Vis Sci. 1992. PMID: 1634353

6

Mitochondrial DNA mutation in a Chinese family with myoclonic epilepsy and ragged-red fiber disease.

Shih KD, Yen TC, Pang CY, Wei YH. Shih KD, et al. Among authors: wei yh. Biochem Biophys Res Commun. 1991 Feb 14;174(3):1109-16. doi: 10.1016/0006-291x(91)91535-k. Biochem Biophys Res Commun. 1991. PMID: 1900002

7

Absence of 4,977-bp deletion of blood cell mitochondrial DNA in patients with young-onset Parkinson's disease.

Shan DE, Yeh SI, Wan YC, Wei YH. Shan DE, et al. Among authors: wei yh. Acta Neurol Scand. 1995 Feb;91(2):149-52. doi: 10.1111/j.1600-0404.1995.tb00423.x. Acta Neurol Scand. 1995. PMID: 7785427

8

A specific 4977-bp deletion of mitochondrial DNA in human ageing skin.

Yang JH, Lee HC, Lin KJ, Wei YH. Yang JH, et al. Among authors: wei yh. Arch Dermatol Res. 1994;286(7):386-90. doi: 10.1007/BF00371798. Arch Dermatol Res. 1994. PMID: 7818280

9

Comparison of mitochondrial DNA polymorphism between Chinese subjects and patients with mitochondrial myopathy.

Yen TC, Wei YH. Yen TC, et al. Among authors: wei yh. Zhonghua Yi Xue Za Zhi (Taipei). 1993 Jan;51(1):1-6. Zhonghua Yi Xue Za Zhi (Taipei). 1993. PMID: 8095846

10

Molecular diagnosis of Leber's hereditary optic neuropathy.

Yen MY, Liu JH, Pang CY, Wei YH. Yen MY, et al. Among authors: wei yh. J Formos Med Assoc. 1993 Jan;92(1):42-5. J Formos Med Assoc. 1993. PMID: 8099825

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