Wei YH - Search Results

1

Genetic analysis in Leber's hereditary optic neuropathy using the comparative genomic hybridization technique.

Yen MY, Chen YJ, Lin CH, Wang AG, Wei YH. Yen MY, et al. Among authors: wei yh. Clin Exp Ophthalmol. 2003 Oct;31(5):435-8. doi: 10.1046/j.1442-9071.2003.00692.x. Clin Exp Ophthalmol. 2003. PMID: 14516433

2

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

3

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

4

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.

5

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

6

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

7

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

8

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

9

Molecular epidemiologic study of mitochondrial DNA mutations in patients with mitochondrial diseases in Taiwan.

Pang CY, Huang CC, Yen MY, Wang EK, Kao KP, Chen SS, Wei YH. Pang CY, et al. Among authors: wei yh. J Formos Med Assoc. 1999 May;98(5):326-34. J Formos Med Assoc. 1999. PMID: 10420700

10

False positive molecular diagnosis of Leber's hereditary optic neuropathy.

Yen MY, Wang AG, Chang WL, Hsu WM, Liu JH, Wei YH. Yen MY, et al. Among authors: wei yh. Zhonghua Yi Xue Za Zhi (Taipei). 2000 Dec;63(12):864-8. Zhonghua Yi Xue Za Zhi (Taipei). 2000. PMID: 11195136

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