Pang CY - Search Results

1

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: pang cy. Invest Ophthalmol Vis Sci. 1992 Jul;33(8):2561-6. Invest Ophthalmol Vis Sci. 1992. PMID: 1634353

2

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: pang cy. Biochem Int. 1992 Mar;26(3):457-68. Biochem Int. 1992. PMID: 1627156

3

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: pang cy. 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

4

Distribution and clinical expression of the tRNA(Lys) mutation in mitochondrial DNA in MERRF syndrome.

Huang CC, Chu NS, Shih KD, Pang CY, Wei YH. Huang CC, et al. Among authors: pang cy. J Formos Med Assoc. 1995 Apr;94(4):159-63. J Formos Med Assoc. 1995. PMID: 7606176

5

Molecular diagnosis of Leber's hereditary optic neuropathy.

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

6

Differential accumulations of 4,977 bp deletion in mitochondrial DNA of various tissues in human ageing.

Lee HC, Pang CY, Hsu HS, Wei YH. Lee HC, et al. Among authors: pang cy. Biochim Biophys Acta. 1994 Apr 12;1226(1):37-43. doi: 10.1016/0925-4439(94)90056-6. Biochim Biophys Acta. 1994. PMID: 8155737

7

MELAS syndrome associated with a tandem duplication in the D-loop of mitochondrial DNA.

Li JY, Kong KW, Chang MH, Cheung SC, Lee HC, Pang CY, Wei YH. Li JY, et al. Among authors: pang cy. Acta Neurol Scand. 1996 Jun;93(6):450-5. doi: 10.1111/j.1600-0404.1996.tb00025.x. Acta Neurol Scand. 1996. PMID: 8836308

8

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. J Formos Med Assoc. 1999 May;98(5):326-34. J Formos Med Assoc. 1999. PMID: 10420700

9

Heteroplasmic mitochondrial DNA mutation in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.

Chiang LM, Jong YJ, Huang SC, Tsai JL, Pang CY, Lee HC, Wei YH. Chiang LM, et al. Among authors: pang cy. J Formos Med Assoc. 1995 Jan-Feb;94(1-2):42-7. J Formos Med Assoc. 1995. PMID: 7613232 Review.

10

MELAS syndrome: correlation between clinical features and molecular genetic analysis.

Liou CW, Huang CC, Chee EC, Jong YJ, Tsai JL, Pang CY, Lee HC, Wei YH. Liou CW, et al. Among authors: pang cy. Acta Neurol Scand. 1994 Nov;90(5):354-9. doi: 10.1111/j.1600-0404.1994.tb02737.x. Acta Neurol Scand. 1994. PMID: 7887136

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