Projects per year
Personal profile
Education
- 國立成功大學學士後醫學系學士
Research Interests
- 皮膚學
- 皮膚外科
- 小兒皮膚科
- 分子生物學
- 美容醫學
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Dive into the research topics where Sheau-Chiou Chao is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Recent external collaboration on country level. Dive into details by clicking on the dots or
Projects
- 7 Finished
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在Hailey-Hailey disease患者的重建表皮上,類固醇、cyclosporine、tacrolimus、蛋白??抑制劑及維他命A酸等化合物對凝血?■楖`素、細胞橋小體及黏連分子表現的影響
05-08-01 → 06-07-31
Project: Research project
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Research output
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Plectin missense mutation p.Leu319pro in the pathogenesis of autosomal recessive epidermolysis bullosa simplex
Tu, W. T., Chen, P. C., Hou, P. C., Huang, H. Y., Wang, J. Y., Chao, S. C., Lee, J. Y. Y., McGrath, J. A., Natsuga, K. & Hsu, C. K., 2020 Aug, In: Acta Dermato-Venereologica. 100, 15, p. 1-2 2 p., adv00242.Research output: Contribution to journal › Article › peer-review
Open Access -
Exertional plantar blistering as an easily overlooked clue for epidermolysis bullosa simplex
Yang, H. S., Yang, C. C., Hsu, C. K., Lee, J., Chao, S. C. & Tu, W. T., 2019 Jul 1, In: Dermatologica Sinica. 37, 3, p. 170-171 2 p.Research output: Contribution to journal › Letter › peer-review
Open Access -
Scleritis and anterior uveitis may herald the development of an epibulbar tumor in patients with extranodal Rosai-Dorfman disease: A case report
Lee, Y. K., Chao, S. C., Lee, C. N. & Hung, J. H., 2019 Jul 10, In: BMC Ophthalmology. 19, 1, 144.Research output: Contribution to journal › Article › peer-review
Open Access -
Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica
Onoufriadis, A., Hsu, C. K., Eide, C. R., Nanda, A., Orchard, G. E., Tomita, K., Sheriff, A., Scott, W., Tierney, C., Lee, J. Y. W., Gomaa, N. S., Desomchoke, R., Lwin, S. M., Tu, W. T., Chen, L. Y., Huang, H. Y., Chao, S. C., Yu-Yun Lee, J., Bare, Y., Hayday, T. & 12 others, , 2019 Dec, In: Journal of Investigative Dermatology. 139, 12, p. 2550-2554.e9Research output: Contribution to journal › Article › peer-review
2 Citations (Scopus) -
Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A
Hsu, T. C., Lee, J. Y. Y., Hsu, M. M. L. & Chao, S. C., 2018 Apr, In: Journal of Dermatology. 45, 4, p. 475-478 4 p.Research output: Contribution to journal › Article › peer-review
1 Citation (Scopus)