Zobrazeno 1 - 10
of 184
pro vyhledávání: '"Sheau-Chiou Chao"'
Autor:
Wei-Ting Tu, Ping-Chen Hou, Peng-Chieh Chen, Wan-Rung Chen, Hsin-Yu Huang, Jing-Yu Wang, Yi-Ting Huang, Yi-Huei Wu, Chun-Lin Su, Yen-An Tang, Hiroaki Iwata, Ken Natsuga, Sheau-Chiou Chao, H. Sunny Sun, Ming-Jer Tang, Julia Yu-Yun Lee, John A. McGrath, Chao-Kai Hsu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-10 (2022)
Abstract Background Epidermolysis bullosa (EB) is a heterogeneous group of hereditary skin diseases characterized by skin fragility. Primary data on Taiwanese population remain scarce. Methods We gathered clinical information from EB patients at Nati
Externí odkaz:
https://doaj.org/article/0cb4dd617c1d453a9b25ad879496557a
Publikováno v:
Journal of Microbiology, Immunology and Infection, Vol 55, Iss 3, Pp 558-560 (2022)
Externí odkaz:
https://doaj.org/article/3fe77e299ddb47bfbc108971b08cbf52
Autor:
Hui-Peng Huang, Chao-Kai Hsu, Sheau-Chiou Chao, Chao-Chun Yang, Gwo-Shing Chen, Chih-Hung Lin, Chang-Ming Huang, Julia Yu-Yun Lee
Publikováno v:
Dermatologica Sinica, Vol 39, Iss 3, Pp 132-136 (2021)
Eosinophilic pustular folliculitis (EPF) is classified into Ofuji disease, immunosuppression-associated EPF, and infancy-associated EPF. The association of EPF with Demodex infestation is rarely reported. We report five cases of EPF with Demodex over
Externí odkaz:
https://doaj.org/article/1e59052d221e464bb94c713f26988a4e
Publikováno v:
Indian Journal of Dermatology, Vol 67, Iss 5, Pp 606-607 (2022)
Externí odkaz:
https://doaj.org/article/e4f6ff48d3084747a2dc95ee90afc97f
Publikováno v:
BMC Ophthalmology, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Rosai-Dorfman disease is a rare non–Langerhans cell histiocytosis. Ocular involvement is even rarer, mostly involving the orbit and eyelids, although marginal corneal ulcers, uveitis, and epibulbar masses have also been reported
Externí odkaz:
https://doaj.org/article/2f249315e66e44e1a229c60df08e7d7b
Autor:
Wei-Ting Tu, Peng-Chieh Chen, Ping-Chen Hou, Hsin-Yu Huang, Jing-Yu Wang, Sheau-Chiou Chao, Julia Yu-Yun Lee, John A. McGrath, Ken Natsuga, Chao-Kai Hsu
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 15, p adv00242 (2020)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/62a1e2ceb1274383aaed80246647898a
Autor:
Yu-Chen Chen, Yi-Ting Huang, Chao-Chun Yang, Edward Chia-Cheng Lai, Cheng-Han Liu, Chao-Kai Hsu, Tak-Wah Wong, Sheau-Chiou Chao, Hamm-Ming Sheu, Chaw-Ning Lee
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0244620 (2020)
BackgroundReal-world clinical data on psoriasis patients receiving different biological agents is needed, especially in Asian populations.ObjectivesOur aim is to compare and analyze the efficacy and safety profile of four biological agents (etanercep
Externí odkaz:
https://doaj.org/article/9d9b0a4a870c42b49534adbcaf3bb0a8
Publikováno v:
Dermatologica Sinica, Vol 37, Iss 2, Pp 103-105 (2019)
Porokeratotic eccrine ostial and dermal duct nevus or porokeratotic eccrine nevus (PEN) is a rare nevoid condition characterized by asymptomatic spiny, keratotic papules, and plaques in linear distribution along Blaschko's lines on the extremities cl
Externí odkaz:
https://doaj.org/article/85c6a5feb2f6478d8e6fb79e6d339a6a
Publikováno v:
Dermatologica Sinica, Vol 36, Iss 4, Pp 200-202 (2018)
Cerebrotendinous xanthomatosis (CTX), a rare autosomal recessive lipid storage disorder which is caused by mutations in gene CYP27A1 leads to deficiency of enzyme sterol 27-hydroxylase. Clinically, CTX is characterized by tendon xanthomas, premature
Externí odkaz:
https://doaj.org/article/892b8b6a97c24f2a9243175ee31160f6
Autor:
Hsing-San Yang, Chao-Chun Yang, Chao-Kai Hsu, Julia Yu-Yun Lee, Sheau-Chiou Chao, Wei-Ting Tu
Publikováno v:
Dermatologica Sinica, Vol 37, Iss 3, Pp 170-171 (2019)
Externí odkaz:
https://doaj.org/article/ce6f4218551044718bae6618387e1cf1