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Showing items 1-4 of 4 (1 Page(s) Totally)
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| 臺大學術典藏 |
2021-06-10T07:29:35Z |
A systematic review of late-onset and very-late-onset multiple acyl-coenzyme A dehydrogenase deficiency: Cohort analysis and patient report from Taiwan
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Kuo, Yih-Chih; Hsueh, Hsueh-Wen; Hsueh, Sung-Ju; Lee, Ni-Chung; Hsieh, Ming-Ju; Chao, Chi-Chao; YIN-HSIU CHIEN; Huang, Pei-Hsin; Yang, Chih-Chao |
| 臺大學術典藏 |
2021-04-23T06:44:08Z |
A systematic review of late-onset and very-late-onset multiple acyl-coenzyme A dehydrogenase deficiency: Cohort analysis and patient report from Taiwan
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Kuo, Yih-Chih; Hsueh, Hsueh-Wen; Hsueh, Sung-Ju; Lee, Ni-Chung; MING-JU HSIEH; Chao, Chi-Chao; Chien, Yin-Hsiu; Huang, Pei-Hsin; Yang, Chih-Chao |
| 臺大學術典藏 |
2020-12-10T01:22:45Z |
Autosomal dominant cerebellar ataxia, deafness, and narcolepsy with amenorrhea, subclinical optic atrophy, and electroencephalographic abnormality: A case report
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Chang, Kai-Chieh;Kuo, Yih-Chih;Hsueh, Hsueh-Wen;Ni-Chung Lee;Yang, Chih-Chao;Hsieh, Sung-Tsang;Chao, Chi-Chao; Chang, Kai-Chieh; Kuo, Yih-Chih; Hsueh, Hsueh-Wen; NI-CHUNG LEE; Yang, Chih-Chao; Hsieh, Sung-Tsang; Chao, Chi-Chao |
| 臺大學術典藏 |
2020-12-10T01:22:45Z |
Autosomal dominant cerebellar ataxia, deafness, and narcolepsy with amenorrhea, subclinical optic atrophy, and electroencephalographic abnormality: A case report
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Chang, Kai-Chieh;Kuo, Yih-Chih;Hsueh, Hsueh-Wen;Ni-Chung Lee;Yang, Chih-Chao;Hsieh, Sung-Tsang;Chao, Chi-Chao; Chang, Kai-Chieh; Kuo, Yih-Chih; Hsueh, Hsueh-Wen; NI-CHUNG LEE; Yang, Chih-Chao; Hsieh, Sung-Tsang; Chao, Chi-Chao |
Showing items 1-4 of 4 (1 Page(s) Totally)
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