Literature DB >> 29578632

A case of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP) with the emphasis on cutaneous histopathological findings.

V Kazlouskaya1, E J Feldman2, J Jakus1, E Heilman1, S Glick1.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2018        PMID： 29578632     DOI： 10.1111/jdv.14968

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN： 0926-9959            Impact factor:   6.166


× No keyword cloud information.
  2 in total

Review 1.  Mutations within the putative protease domain of the human FAM111B gene may predict disease severity and poor prognosis: A review of POIKTMP cases.

Authors:  Afolake Arowolo; Cenza Rhoda; Nonhlanhla Khumalo
Journal:  Exp Dermatol       Date:  2022-02-13       Impact factor: 4.511

Review 2.  Proposed Cellular Function of the Human FAM111B Protein and Dysregulation in Fibrosis and Cancer.

Authors:  Afolake Arowolo; Moses Malebana; Falone Sunda; Cenza Rhoda
Journal:  Front Oncol       Date:  2022-07-04       Impact factor: 5.738
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.