Home About us Articles Multimedia Search Instructions Login 
5 years IF: 1.036 (® Thomson Reuters)
IF 2016: 1.064 (® Thomson Reuters)
Total Cites: 7140
Follow Us
Follow Us
  • Users Online: 73
  • Home
  • Print this page
  • Email this page

    Article Cited by others


Novel Mutations in PSENEN Gene in Two Chinese Acne Inversa Families Manifested as Familial Multiple Comedones and Dowling-Degos Disease

Zhou Cheng, Wen Guang-Dong, Soe Lwin Myint, Xu Hong-Jun, Du Juan, Zhang Jian-Zhong

Year : 2016| Volume: 129| Issue : 23 | Page no: 2834-2839

   This article has been cited by
1 Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authors
M. Pavlovsky,O. Sarig,M. Eskin-Schwartz,A. Hafner,E. Sprecher
British Journal of Dermatology. 2018;
[Pubmed]  [Google Scholar] [DOI]
2 A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENEN
M. Pavlovsky,O. Sarig,M. Eskin-Schwartz,N. Malchin,R. Bochner,J. Mohamad,A. Gat,A. Peled,A. Hafner,E. Sprecher
British Journal of Dermatology. 2017;
[Pubmed]  [Google Scholar] [DOI]
3 PSENEN Mutation Carriers with Co-manifestation of Acne Inversa (AI) and Dowling-Degos Disease (DDD): Is AI or DDD the Subphenotype?
Chengrang Li,Wenrui Li,Haoxiang Xu,Xiaofeng Zhang,Bin Su,Wanlu Zhang,Xue Zhang,Baoxi Wang
Journal of Investigative Dermatology. 2017; 137(10): 2234
[Pubmed]  [Google Scholar] [DOI]


Read this article