Literature DB >> 12835558

A nonfamilial Japanese case of Huriez syndrome: p53 expression in squamous cell carcinoma.

Eri Watanabe, Toshihiro Takai, Masamitsu Ichihashi, Masato Ueda.   

Abstract

Entities:  

Mesh：

Year:  2003        PMID： 12835558     DOI： 10.1159/000070951

Source DB:  PubMed          Journal:  Dermatology        ISSN： 1018-8665            Impact factor:   5.366


× No keyword cloud information.
  4 in total

1.  A Rare Syndrome Resembling Scleroderma: Huriez Syndrome.

Authors:  Nil Su Çelik; Şirin Yaşar; Sema Aytekin; Pembegül Güneş
Journal:  Skin Appendage Disord       Date:  2017-08-12

2.  Finger Pad Squamous Cell Carcinoma: Report of Squamous Cell Carcinoma of the Distal Palmar Digit and Review of Associated Risk Factors, Mimickers, and Treatment of Squamous Cell Carcinoma of Ventral Hand Digits.

Authors:  Philip R Cohen; S Brian Jiang
Journal:  J Clin Aesthet Dermatol       Date:  2017-08-01

3.  Poikiloderma a varied presentation - Huriez syndrome.

Authors:  Priyadarshini Kharge; Carol Fernendes; Vijayeeta Jairath; Madan Mohan; Suresh Chandra
Journal:  Indian Dermatol Online J       Date:  2015 Jan-Feb

4.  A novel mutation in TRPV3 gene causes atypical familial Olmsted syndrome.

Authors:  Cheng Ni; Ming Yan; Jia Zhang; Ruhong Cheng; Jianying Liang; Dan Deng; Zhen Wang; Ming Li; Zhirong Yao
Journal:  Sci Rep       Date:  2016-02-23       Impact factor: 4.379
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.