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The Journal of Dermatology|December 8, 2022
A possible role for second-hit postzygotic GJB2 mutation in porokeratotic eccrine ostial and dermal duct nevusYi-Han Chang, Hsing-San Yang, Hsin-Yu Huang, et al.Yi Chuan = Hereditas|January 11, 2005
[Compatible-solute-supported periplasmic expression of recombinant immunotoxins and the effects of glucose thereby]Yong-Ming Ren, Ming-Sheng Zhang, Dan He, et al.Journal of Tissue Viability|November 17, 2020
Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept studyTak-Wah Wong, Chao-Chun Yang, Chao-Kai Hsu, et al.Comprehensive Reviews in Food Science and Food Safety|March 31, 2022
S-Allyl cysteine in garlic (Allium sativum): Formation, biofunction, and resistance to food processing for value-added product developmentBara Yudhistira, Fuangfah Punthi, Jer-An Lin, et al.Journal of Personalized Medicine|March 29, 2023
Higher-Order Aberrations of Topography-Guided LASIK and Wavefront-Optimized LASIK in High- and Low-Myopic Eyes: A Non-Randomized Controlled TrialElsa Lin-Chin Mai, Chao-Kai Chang, Chia-Yi Lee, et al.Journal of Dermatological Science|December 17, 2021
Current topics in Epidermolysis bullosa: Pathophysiology and therapeutic challengesKen Natsuga, Satoru Shinkuma, Chao-Kai Hsu, et al.American Journal of Clinical Dermatology|July 22, 2021
Investigational Treatments for Epidermolysis BullosaPing-Chen Hou, Han-Tang Wang, Stasha Abhee, et al.Journal of Studies on Alcohol and Drugs|February 17, 2023
A Pilot Study of an Evidence-Based Prevention Intervention (keepin' it REAL) for Early Adolescents in Kenyan SchoolsFlavio F Marsiglia, Stephen S Kulis, Samuel Munyuwiny, et al.The Journal of Dermatology|October 16, 2025
Oral Statin Therapy in KRT16- and KRT17-Associated Palmoplantar Epidermal Differentiation Disorder (Pachyonychia Congenita)Sota Itamoto, Wei-Ting Tu, Chih-Yu Chang, et al.Frontiers in Genetics|October 10, 2022
Case Report: A novel desmoplakin mutation in a taiwanese woman with familial dilated cardiomyopathy that necessitated heart transplantationYi-Han Chang, Pei Lin, Jia-Ling Lin, et al.Pageof 33