Literature DB >> 13149722

Congenital poikiloderma with traumatic bulla formation and progressive cutaneous atrophy.

T KINDLER.   

Abstract

Entities:  

Keywords:  EPIDERMOLYSIS BULLOSA/complications; POIKILODERMA ATROPHICANS VASCULARE/complications

Mesh：

Year:  1954        PMID： 13149722     DOI： 10.1111/j.1365-2133.1954.tb12598.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


× No keyword cloud information.
  46 in total

1.  Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.

Authors:  Dawn H Siegel; Gabrielle H S Ashton; Homero G Penagos; James V Lee; Heidi S Feiler; Kirk C Wilhelmsen; Andrew P South; Frances J D Smith; Alan R Prescott; Vesarat Wessagowit; Noritaka Oyama; Masashi Akiyama; Daifullah Al Aboud; Khalid Al Aboud; Ahmad Al Githami; Khalid Al Hawsawi; Abla Al Ismaily; Raouf Al-Suwaid; David J Atherton; Ruggero Caputo; Jo-David Fine; Ilona J Frieden; Elaine Fuchs; Richard M Haber; Takashi Harada; Yasuo Kitajima; Susan B Mallory; Hideoki Ogawa; Sedef Sahin; Hiroshi Shimizu; Yasushi Suga; Gianluca Tadini; Kikuo Tsuchiya; Colin B Wiebe; Fenella Wojnarowska; Adel B Zaghloul; Takahiro Hamada; Rajeev Mallipeddi; Robin A J Eady; W H Irwin McLean; John A McGrath; Ervin H Epstein
Journal:  Am J Hum Genet       Date:  2003-06-03       Impact factor: 11.025

2.  [Forms of congenital poikiloderma].

Authors:  P WODNIANSKY
Journal:  Arch Klin Exp Dermatol       Date:  1957

3.  Epidermolysis bullosa of the newborn.

Authors:  M ROSSET
Journal:  Can Med Assoc J       Date:  1956-09-15       Impact factor: 8.262

Review 4.  Recent advances in the understanding of the molecular mechanisms regulating platelet integrin αIIbβ3 activation.

Authors:  Lanlan Tao; Yue Zhang; Xiaodong Xi; Nelly Kieffer
Journal:  Protein Cell       Date:  2010-07-29       Impact factor: 14.870

5.  CUGC for hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis (POIKTMP).

Authors:  Sébastien Küry; Sandra Mercier; Gasnat Shaboodien; Thomas Besnard; Sébastien Barbarot; Nonhlanhla P Khumalo; Bongani M Mayosi; Stéphane Bézieau
Journal:  Eur J Hum Genet       Date:  2015-10-07       Impact factor: 4.246

6.  A novel large deletion mutation of FERMT1 gene in a Chinese patient with Kindler syndrome.

Authors:  Ying Gao; Jin-li Bai; Xiao-yan Liu; Yu-jin Qu; Yan-yan Cao; Jian-cai Wang; Yu-wei Jin; Hong Wang; Fang Song
Journal:  J Zhejiang Univ Sci B       Date:  2015-11       Impact factor: 3.066

Review 7.  [Hereditary photodermatoses].

Authors:  P Poblete-Gutiérrez; W H C Burgdorf; C Has; M Berneburg; J Frank
Journal:  Hautarzt       Date:  2006-12       Impact factor: 0.751

8.  A Kindler syndrome-associated squamous cell carcinoma treated with radiotherapy.

Authors:  Ademar Caldeira; William Correia Trinca; Thais Pires Flores; Andrea Barleze Costa; Claudio de Sá Brito; Karen Loureiro Weigert; Maryana Schwartzhaupt Matos; Carmela Nicolini; Fernando Mariano Obst
Journal:  Rep Pract Oncol Radiother       Date:  2016-09-10

Review 9.  Kindler syndrome and periodontal disease: review of the literature and a 12-year follow-up case.

Authors:  Colin B Wiebe; Giorgio Petricca; Lari Häkkinen; Guoqiao Jiang; Chuanyue Wu; Hannu S Larjava
Journal:  J Periodontol       Date:  2008-05       Impact factor: 6.993

10.  Kindler syndrome with unique ocular findings.

Authors:  Anchal Thakur; Ashish Kulshreshtha; Sheetanshu Kumar; Sunil Dogra; Amit Gupta
Journal:  Indian J Ophthalmol       Date:  2020-06       Impact factor: 1.848
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.