Results 91 to 100 of about 25,211 (207)

The puzzling effect of disease severity on quality of life in epidermolysis bullosa

Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 8, Page e665-e668, August 2026.
Vinzenz Hübl, Sophie Strobl, Gudrun Salamon, Cristina Has, on behalf of the BUR‐EB Study Group   +4 more
wiley   +1 more source

Expression of Integrins in Junctional and Dystrophic Epidermolysis Bullosa

Journal of Investigative Dermatology, 1990
Recently, monoclonal antibodies (MoAb) have been raised against a family of adhesive membrane receptors (R) for extracellular matrix molecules known as integrins. In order to ascertain whether these adhesive proteins are normally expressed in inherited epidermolysis bullosa (EB) dermal epidermal junction, we studied the reactivity of MoAb recognizing ...
V. Nazzaro, E. Berti, A. Cerri, A. Brusasco, R. Cavalli, R. Caputo   +5 more
openaire   +3 more sources

Glomerulonephritis in Youth With Dystrophic Epidermolysis Bullosa [PDF]

Kidney International Reports, 2021
Erica Hughley, Edward J. Nehus, Katherine VandenHeuvel, Bret D. Augsburger, Namrata G. Jain, Anne W. Lucky   +5 more
openaire   +3 more sources

Ex Vivo COL7A1 Correction for Recessive Dystrophic Epidermolysis Bullosa Using CRISPR/Cas9 and Homology-Directed Repair

Molecular Therapy: Nucleic Acids, 2018
Recessive dystrophic epidermolysis bullosa is a rare and severe genetic skin disease resulting in blistering of the skin and mucosa. Recessive dystrophic epidermolysis bullosa (RDEB) is caused by a wide variety of mutations in COL7A1-encoding type VII ...
Araksya Izmiryan, Clarisse Ganier, Matteo Bovolenta, Alain Schmitt, Fulvio Mavilio, Alain Hovnanian   +5 more
doaj   +1 more source

A case of congenital pyloric atresia with dystrophic epidermolysis bullosa

, 2014
Pyloric atresia with epidermolysis bullosa (EB) dystrophica is a rare entity that may not be immediately recognized. We describe the fourth confirmed case of pyloric atresia associated with the dystrophic subtype of EB diagnosed by standard pathologic ...
Haydel, Dana, Ford, Henri R, Grant, Christa N, Short, Scott S, Merianos, Demetri   +4 more
core   +1 more source

Fluoroscopically guided endoluminal balloon dilation of oesophageal stricture due to dystrophic epidermolysis bullosa in two sisters.

, 2006
Dystrophic epidermolysis bullosa is an inherited disorder with frequent oesophageal stricture formation. There is no satisfactory medical treatment of dysphagia however; endoluminal balloon dilation is a novel method with satisfactory results ...
Karakan, T., ÜNAL, SERHAT, Cindoruk, M., Gorgul, A., Dumlu, S., Dogan, İBRAHİM   +5 more
core  

Recessive dystrophic epidermolysis bullosa: A review of disease pathogenesis and update on future therapies

, 2015
Objective: Review the pathogenesis of recessive dystrophic epidermolysis bullosa and provide an update on research currently underway that is aimed at treating and potentially curing this severe skin disorder. Design: Review article.
Soro, Luis, Bartus, Cynthia, Purcell, Stephen   +2 more
core   +3 more sources

EPIDERMOLYSIS BULLOSA HEREDITARIA: A DERMATOLOGIST‘S PERSPECTIVE AND NEWLY TREATMENT APPROACHES

Slovenska pediatrija
Epidermolysis bullosa is a genetically inherited disorder characterized by extreme skin fragility. Mutations in at least 20 different genes have been identified, leading to structural or functional abnormalities or the absence of proteins involved in the
Olga Točkova
doaj   +1 more source

The tumor microenvironment of cutaneous squamous cell carcinoma in high-risk patient groups: A scoping review

JID Innovations
Cutaneous squamous cell carcinoma (cSCC) is a prevalent skin cancer in the general population that poses so far unresolved challenges in high-risk groups such as organ transplant recipients and individuals with recessive dystrophic epidermolysis bullosa.
Wandong Wang, Clara Harrs, Maria C. Bolling, Barbara Horváth, Gilles F.H. Diercks, Emőke Rácz   +5 more
doaj   +1 more source

Safe Skin Management during Open Hepatectomy in a Patient with Recessive Dystrophic Congenital Epidermolysis Bullosa

Case Reports in Surgery, 2018
Congenital epidermolysis bullosa is a rare, genetic condition in which even slight stimulation can cause blistering of the skin or mucosa. While previous reports of treatments requiring general anesthesia in these patients were focused on anesthesia ...
Ikuo Watanobe, Hiroko Kida, Yuuki Sekine, Masaya Kawai, Shozo Miyano, Michio Machida, Toshiaki Kitabatake, Hiroyuki Sugo, Yoshifumi Lee, Kuniaki Kojima   +9 more
doaj   +1 more source