[1] |
WANG Tianzi, LU Jiliang, LIU Yongxia, TIAN Hongqing.
Three cases with palmoplantar pustulosis successfully treated by tofacitinib
[J]. China Journal of Leprosy and Skin Diseases, 2023, 39(6): 397-402.
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[2] |
FENG Xiaoyan, LU Xinxin, BI Tiantian, LI Qinfeng.
Keratitis ichthyosis deafness syndrome caused by GJB2 gene mutation
[J]. China Journal of Leprosy and Skin Diseases, 2023, 39(6): 423-425.
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[3] |
MIAO Mengyu, WANG Zhenzhen, SUN Lele, LIU Hong, ZHANG Furen.
One novel mutation of the NCSTN gene in one acne inversa family
[J]. China Journal of Leprosy and Skin Diseases, 2021, 37(8): 486-489.
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[4] |
ZHANG Wenqing, YU Xia, LI Ming, YAO Zhirong.
Update of gene mutations associated with Juvenile Xanthogranuloma
[J]. China Journal of Leprosy and Skin Diseases, 2020, 36(2): 117-121.
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[5] |
LI Lulu, FU Xi'an, WANG Zhenzhen, YU Gongqi, LIU Hong, ZHANG Furen.
Detection of IL36RN gene mutation and genotype-phenotype correlation analysis in 107 cases of generalized pustular psoriasis
[J]. China Journal of Leprosy and Skin Diseases, 2019, 35(4): 193-196.
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[6] |
LIU Lian, ZHANG Zihui, HAO Dan, MEI Rong, LI Erlong, SUN Bensen, JIANG Xian.
Advances in the Pathogenesis of Port Wine Stains
[J]. China Journal of Leprosy and Skin Diseases, 2019, 35(4): 253-256.
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[7] |
GUO Yunyi, ZHU Ying, ZHANG Danlu, GUO Birong, SUN Zhonghui.
Mutations detection in two families with epidermolytic palmoplantar keratoderma
[J]. China Journal of Leprosy and Skin Diseases, 2019, 35(12): 727-730.
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[8] |
JI Jin, GUO Qin, ZHANG Ruohua, LI Ming.
Identification of ADAR1 gene mutation in one sporadic case with dyschromatosis symmetrica hereditaria
[J]. China Journal of Leprosy and Skin Diseases, 2018, 34(6): 321-323.
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[9] |
LI Lulu, YOU Jiabao, FU Xian, YU Gongqi, LIU Hong, ZHANG Furen, .
Association of AP1S3 mutation with generalized pustular psoriasis
[J]. China Journal of Leprosy and Skin Diseases, 2018, 34(3): 131-134.
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[10] |
ZENG Rong, LIU Yuzhen, TONG Jianbo, HE Yanyan, LIN Tong, XU Haoxiang, LI Min..
Identification of a novel mutation of ADAR1 gene in a family with dyschromatosis symmetrical hereditaria
[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(9): 517-519.
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[11] |
ZENG Rong, HE Yanyan, HUI Yun, LI Zhiliang, XU Haoxiang, LI Min..
Identification of a novel mutation of KRT9 gene in a family with epidermolytic palmoplantar keratoderma
[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(8): 465-467.
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[12] |
CHEN Fuying, LI Ming..
Update of the abnormal cholesterol metabolism and keratinization genodermatosis
[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(8): 506-509.
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[13] |
CHEN Pingjiao, LI Changxing, ZENG Kang, ZHANG Xibao..
Update of the genetics of bullous congenital ichthyosiform erythroderma
[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(6): 381-384.
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[14] |
CAO Jing, SUN Lele, FU Xian, WANG Zhenzhen, YU Gongqi, LIU Hong, ZHANG Furen.
Detection of KTR gene mutations in a family with pachyonychia congenital type II
[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(2): 70-73.
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[15] |
TANG Zhuangli, WANG Tian, XIAO Shengxiang, WANG Xiaopeng..
Gene mutation detection and bioinformatical analysis of Keratin9-gene in one pedigree of epidermolytic palmoplantar keratoderma
[J]. China Journal of Leprosy and Skin Diseases, 2017, 33(12): 709-711,716.
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