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Journal of Dermatological Science|September 23, 2021
Amyloidosis cutis dyschromica cases caused by GPNMB mutations with different inheritance patternsWen Qin, Huijun Wang, Weilong Zhong, et al.Journal of Dermatological Science|March 1, 2025
A signal peptide variant in SLURP1 with dominant-negative effect causes progressive symmetric erythrokeratodermiaZhuoqing Gong, Yunran Peng, Sisi Zhao, et al.European Journal of Dermatology : EJD|July 17, 2024
Unilateral focal palmoplantar keratoderma associated with a postzygotic variant in PIK3CA and activation of the PI3K/AKT/mTOR pathwayZhuoqing Gong, Sha Peng, Huijun Wang, et al.The Journal of Dermatology|June 22, 2021
Novel pathogenic variants in the RECQL4 gene causing Rothmund-Thomson syndrome in three Chinese patientsYingzi Zhang, Wen Qin, Huijun Wang, et al.The Journal of Dermatology|June 26, 2024
Dermatopathological features and successful treatment with topical antioxidant for ichthyosiform lesions in Mitchell syndrome caused by an ACOX1 variantZhuoqing Gong, Sai Yang, Shiqi Ling, et al.The British Journal of Dermatology|January 23, 2023
Variants in KLK11, affecting signal peptide cleavage of kallikrein-related peptidase 11, cause an autosomal-dominant cornification disorderZhuoqing Gong, Shangzhi Dai, Xingyuan Jiang, et al.Pediatric Dermatology|April 21, 2010
A case of Hailey-Hailey disease in an infant with a new ATP2C1 gene mutationZhe Xu, Lixin Zhang, Yuanyuan Xiao, et al.European Journal of Dermatology : EJD|August 28, 2024
Symmetrical acral keratoderma associated with new variants in the filaggrin geneWanting Luo, Qiaoyun Lu, Yangyang Jiang, et al.Frontiers in Cellular and Infection Microbiology|June 10, 2025
A novel loss-of-function variant in STAT1 causes Mendelian susceptibility to mycobacterial diseaseKunlun Lv, Zhuoqing Gong, Yiting Fu, et al.Molecular Pain|February 10, 2018
TRPV1 gain-of-function mutation impairs pain and itch sensations in miceLina Duo, Linghan Hu, Naxi Tian, et al.Pageof 731