Huang CC - Search Results

1

Low antioxidant content and mutation load in mitochondrial DNA A3243G mutation-related diabetes mellitus.

Liou CW, Huang CC, Lee CF, Lin TK, Wei YH. Liou CW, et al. Among authors: huang cc. J Formos Med Assoc. 2003 Aug;102(8):527-33. J Formos Med Assoc. 2003. PMID: 14569316

2

Sensory neuropathy in X-linked recessive bulbospinal neuronopathy.

Chu CC, Huang CC, Kuo HC, Liu CS, Tsai CS. Chu CC, et al. Among authors: huang cc. J Formos Med Assoc. 2002 Mar;101(3):214-8. J Formos Med Assoc. 2002. PMID: 12051019

3

Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies.

Huang CC, Kuo HC, Chu CC, Liou CW, Ma YS, Wei YH. Huang CC, et al. J Biomed Sci. 2002;9(6 Pt 1):527-33. doi: 10.1159/000064725. J Biomed Sci. 2002. PMID: 12372990

4

Clinical features of Leber's hereditary optic neuropathy with the 11778 mitochondrial DNA mutation in Taiwanese patients.

Hung HL, Kao LY, Huang CC. Hung HL, et al. Among authors: huang cc. Chang Gung Med J. 2003 Jan;26(1):41-7. Chang Gung Med J. 2003. PMID: 12656308 Free article.

5

Maternally inherited diabetes and deafness (MIDD) syndrome: a clinical and molecular genetic study of a Taiwanese family.

Chen YN, Liou CW, Huang CC, Lin TK, Wei YH. Chen YN, et al. Among authors: huang cc. Chang Gung Med J. 2004 Jan;27(1):66-73. Chang Gung Med J. 2004. PMID: 15074893 Free article.

6

Cavernous sinus thrombosis and cerebral infarction caused by Fusobacterium nucleatum infection.

Chang CS, Liou CW, Huang CC, Lui CC, Chang KC. Chang CS, et al. Among authors: huang cc. Chang Gung Med J. 2004 Jun;27(6):459-63. Chang Gung Med J. 2004. PMID: 15455548 Free article.

7

Study of a Taiwanese family with oculopharyngeal muscular dystrophy.

Kuo HC, Chen CM, Lee-Chen GJ, Hu FJ, Chu CC, Liou CW, Huang CC. Kuo HC, et al. Among authors: huang cc. J Neurol Sci. 2009 Mar 15;278(1-2):21-4. doi: 10.1016/j.jns.2008.11.001. Epub 2008 Dec 20. J Neurol Sci. 2009. PMID: 19101703

8

[Mitochondrial disease and mitochondrial DNA depletion syndromes].

Huang CC, Hsu CH. Huang CC, et al. Acta Neurol Taiwan. 2009 Dec;18(4):287-95. Acta Neurol Taiwan. 2009. PMID: 20329599 Review. Chinese.

9

Chronic progressive external ophthalmoplegia with T9957C mitochondrial DNA mutation in a Taiwanese patient.

Liu CH, Liou CW, Liu CH, Kuo HC, Chu CC, Huang CC. Liu CH, et al. Among authors: huang cc. Acta Neurol Taiwan. 2011 Mar;20(1):53-8. Acta Neurol Taiwan. 2011. PMID: 21249588

10

Prognosis of symptomatic patients with the A3243G mutation of mitochondrial DNA.

Liu CH, Chang CH, Kuo HC, Ro LS, Liou CW, Wei YH, Huang CC. Liu CH, et al. Among authors: huang cc. J Formos Med Assoc. 2012 Sep;111(9):489-94. doi: 10.1016/j.jfma.2011.06.014. Epub 2012 Apr 18. J Formos Med Assoc. 2012. PMID: 23021505 Free article.

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