Wei YH - Search Results

1

Association of the Y402H polymorphism in complement factor H gene and neovascular age-related macular degeneration in Chinese patients.

Lau LI, Chen SJ, Cheng CY, Yen MY, Lee FL, Lin MW, Hsu WM, Wei YH. Lau LI, et al. Among authors: wei yh. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3242-6. doi: 10.1167/iovs.05-1532. Invest Ophthalmol Vis Sci. 2006. PMID: 16877387

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 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

4

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

5

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

6

Compensatory elevation of complex II activity in Leber's hereditary optic neuropathy.

Yen MY, Lee HC, Liu JH, Wei YH. Yen MY, et al. Among authors: wei yh. Br J Ophthalmol. 1996 Jan;80(1):78-81. doi: 10.1136/bjo.80.1.78. Br J Ophthalmol. 1996. PMID: 8664239 Free PMC article.

7

Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.

Yen MY, Wei YH, Liu JH. Yen MY, et al. Among authors: wei yh. J Neuroophthalmol. 1996 Jun;16(2):120-3. J Neuroophthalmol. 1996. PMID: 8797169

8

Peripapillary fluorescein leakage in 11778 Leber's optic neuropathy.

Yen MY, Wei YH, Liu JH. Yen MY, et al. Among authors: wei yh. J Neuroophthalmol. 1996 Sep;16(3):178-81. J Neuroophthalmol. 1996. PMID: 8865009

9

Energy charge is not decreased in lymphocytes of patients with Leber's hereditary optic neuropathy with the 11,778 mutation.

Yen MY, Lee JF, Liu JH, Wei YH. Yen MY, et al. Among authors: wei yh. J Neuroophthalmol. 1998 Jun;18(2):84-5. J Neuroophthalmol. 1998. PMID: 9621261

10

Exclusive homoplasmic 11778 mutation in mitochondrial DNA of Chinese patients with Leber's hereditary optic neuropathy.

Yen MY, Lee HC, Wang AG, Chang WL, Liu JH, Wei YH. Yen MY, et al. Among authors: wei yh. Jpn J Ophthalmol. 1999 May-Jun;43(3):196-200. doi: 10.1016/s0021-5155(99)00008-8. Jpn J Ophthalmol. 1999. PMID: 10413253

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