每年研究成果
指紋 查看啟用 Rai-Hseng Hsu 的研究主題。這些主題標籤來自此人的作品。共同形成了獨特的指紋。
Biotinidase Deficiency
Medicine & Life Sciences
Congenital Generalized Lipodystrophy
Medicine & Life Sciences
Taiwan
Medicine & Life Sciences
Population
Medicine & Life Sciences
Phenotype
Medicine & Life Sciences
Genotype
Medicine & Life Sciences
Newborn Infant
Medicine & Life Sciences
Laryngomalacia
Medicine & Life Sciences
網絡
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研究成果 2019 2019
- 4 引文
- 1 h-指數
- 3 文章
3
引文
(Scopus)
Congenital generalized lipodystrophy in Taiwan
Hsu, R. H., Lin, W. D., Chao, M. C., Hsiao, H. P., Wong, S. L., Chiu, P. C., Chu, S. Y., Ke, Y. Y., Lau, B. H., Chien, Y. H., Hwu, W. L., Tsai, F. J., Wang, C. H. & Lee, N. C., 一月 2019, 於 : Journal of the Formosan Medical Association. 118, 1P1, p. 142-147 6 p.研究成果: 雜誌貢獻 › 文章
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Congenital Generalized Lipodystrophy
Taiwan
Leptin
Genotype
Acanthosis Nigricans
1
引文
(Scopus)
Genotypic and phenotypic correlations of biotinidase deficiency in the Chinese population
Hsu, R. H., Chien, Y. H., Hwu, W. L., Chang, I. F., Ho, H. C., Chou, S. P., Huang, T. M. & Lee, N. C., 一月 7 2019, 於 : Orphanet Journal of Rare Diseases. 14, 1, 6.研究成果: 雜誌貢獻 › 文章
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Biotinidase Deficiency
Population
Newborn Infant
Phenotype
Laryngomalacia
Next-generation sequencing identifies TRPV4-related skeletal dysplasia in a boy with progressive bowlegs
Hsu, R. H., Hwu, W. L., Chen, M., Chung, I. F., Peng, S. S. F., Chen, C. Y., Cheng, W. C., Chien, Y. H. & Lee, N. C., 二月 2019, 於 : Pediatrics and Neonatology. 60, 1, p. 102-104 3 p.研究成果: 雜誌貢獻 › 文章
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