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	1.	Is SAPHO Syndrome Linked to PASH Syndrome and Hidradenitis Suppurativa by Nicastrin Mutation? A Case Report. [electronic resource] by Li, Chengrang Xu, Haoxiang Wang, Baoxi Producer: 20191114 In: The Journal of rheumatology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel missense mutation of the ATP2C1 gene in a Chinese patient with papular acantholytic dermatosis of the anogenital area. [electronic resource] by Xiao, Xuemin Chen, LiHong Wang, Baoxi Li, Chengrang Producer: 20170406 In: Indian journal of dermatology, venereology and leprology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutation p.R156H of KRT10 responsible for severe phenotype of epidermolytic ichthyosis in a Chinese family. [electronic resource] by Li, Zhiliang Liu, Qiao Wang, Aimin Wang, Hongsheng Li, Chengrang Producer: 20140912 In: Therapeutics and clinical risk management vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Hidradenitis suppurativa is treated with low-dose flutamide. [electronic resource] by Li, Chengrang Xu, Haoxiang Zhang, Xiaofeng Zhang, Wanlu He, Yanyan Wang, Baoxi Producer: 20190813 In: The Journal of dermatology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Identification of two novel mutations in Chinese patients with Dyschromatosis symmetrica hereditaria. [electronic resource] by Li, Ming Li, Chengrang Hua, Haikang Zhu, Wenyuan Lu, Yan Yang, Lijia Producer: 20060104 In: Archives of dermatological research vol. 297 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Coexistence of porokeratosis ptychotropica with porokeratosis of Mibelli in a Chinese man. [electronic resource] by Ma, Yiping Li, Chengrang Wu, Jianbing Cui, Pangen Lin, Lin Feng, Suying Producer: 20150914 In: Postepy dermatologii i alergologii vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Optimization of the method for the culture of melanocyte precursors from hair follicles and their activation by 1,25-dihydroxyvitamin D3. [electronic resource] by Wang, Daguang Xu, Xihui Ma, Huijun Yue, Xuezhuang Li, Chengrang Zhu, Wenyuan Publication details: Experimental and therapeutic medicine Oct 2013 In: Experimental and therapeutic medicine vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Hypermethylation of HLA-C may be an epigenetic marker in psoriasis. [electronic resource] by Chen, Min Wang, Yan Yao, Xu Li, Chengrang Jiang, Mingjun Cui, Pangen Wang, Baoxi Producer: 20170510 In: Journal of dermatological science vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Increased serum interleukin-6 levels in patients with hidradenitis suppurativa. [electronic resource] by Xu, Haoxiang Xiao, Xuemin He, Yanyan Zhang, Xiaofeng Li, Chengrang Mao, Qiuxia Wu, Xinfeng Wang, Baoxi Publication details: Postepy dermatologii i alergologii Feb 2017 In: Postepy dermatologii i alergologii vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	PSENEN Mutation Carriers with Co-manifestation of Acne Inversa (AI) and Dowling-Degos Disease (DDD): Is AI or DDD the Subphenotype? [electronic resource] by Li, Chengrang Li, Wenrui Xu, Haoxiang Zhang, Xiaofeng Su, Bin Zhang, Wanlu Zhang, Xue Wang, Baoxi Producer: 20181008 In: The Journal of investigative dermatology vol. 137 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria. [electronic resource] by Li, Ming Yang, Lijia Li, Chengrang Jin, Cheng Lai, Meiling Zhang, Guolong Hu, Yan Ji, Jin Yao, Zhirong Producer: 20101116 In: Archives of dermatological research vol. 302 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis. [electronic resource] by Yu, Xia Chen, Fuyin Ni, Cheng Zhang, Guolong Zheng, Luyao Zhang, Jia Li, Chengrang Sandilands, Aileen Yao, Zhirong Li, Ming Producer: 20190325 In: The Journal of investigative dermatology vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Nicastrin/miR-30a-3p/RAB31 Axis Regulates Keratinocyte Differentiation by Impairing EGFR Signaling in Familial Acne Inversa. [electronic resource] by He, Yanyan Xu, Haoxiang Li, Chengrang Zhang, Xiaofeng Zhou, Pengjun Xiao, Xuemin Zhang, Wanlu Wu, Yingda Zeng, Rong Wang, Baoxi Producer: 20191031 In: The Journal of investigative dermatology vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos disease. [electronic resource] by Li, Ming Cheng, Ruhong Liang, Jianying Yan, Heng Zhang, Hui Yang, Lijia Li, Chengrang Jiao, Qingqing Lu, Zhiyong He, Jianhui Ji, Jin Shen, Zhu Li, Chunqi Hao, Fei Yu, Hong Yao, Zhirong Producer: 20140109 In: American journal of human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)