Results 101 to 110 of about 25,211 (207)

Type VII collagen is expressed but anchoring fibrils are defective in dystrophic epidermolysis bullosa inversa.

, 1990
A patient with dystrophic epidermolysis bullosa inversa was studied using electron microscopy and indirect immunofluorescence using antibodies to matrix macromolecules of the dermoepidermal junction zone.
Schnyder UW, Kero M, Bruckner-Tuderman L, Reunala T, Niemi KM   +4 more
core   +1 more source

Dystrophic epidermolysis bullosa [PDF]

Indian Pediatrics, 2012
Abhijeet Kumar Jha, Piyush Kumar, Sambeet Kumar Mallik   +2 more
openaire   +1 more source

CASE STUDY: EPIDERMOLYSIS BULLOSA

, 2019
Epidermolysis Bullosa is a group of rare genetic skin conditions, which is characterized by extremely fragile skin and recurrent blister formation, resulting from minor mechanical friction or trauma.
Noman Amanat, Muhammad Afzal, Ms. Hajra sarwar
core   +1 more source

Epidermolysis bullosa pruriginosa

Indian Journal of Dermatology, 2005
Epidermolysis bullosa (EB) pruriginosa is a rare distinct variant of dystrophic EB. It is characterized by extremely pruritic, lichenified or nodular lesions predominantly over legs, milia formation and albopapuloid lesions on the trunk.
Puri Suruchi, Nanda Soni, Grover Chander, Reddy B   +3 more
doaj  

Epidermolysis Bullosa Acquisita Develops in Dominant Dystrophic Epidermolysis Bullosa [PDF]

Journal of Investigative Dermatology, 2016
Hayashi, Ryota, Natsuga, Ken, Watanabe, Mika, Iwata, Hiroaki, Shinkuma, Satoru, Ito, Akiko, Masui, Yukiko, Ito, Masaaki, Shimomura, Yutaka   +8 more
openaire   +2 more sources

Identifying Precision Medicine for Dystrophic Epidermolysis Bullosa

, 2020
University of Minnesota M.S. thesis. December 2020. Major: Clinical Research. Advisor: Logan Spector. 1 computer file (PDF); vi, 72 pages.Background: Dystrophic epidermolysis bullosa (DEB) is a skin blistering disease caused by mutations in the COL7A1 ...
Thompson, Elizabeth
core  

Multicentre phase II open study assessing the efficacy and safety of apremilast in children and adults with epidermolysis bullosa simplex generalised: study protocol for the EBULO study

BMJ Open
Introduction Epidermolysis bullosa (EB) is a group of rare genetic skin disorders characterised by skin and mucosal fragility, leading to painful blisters and erosions.
Annabel Maruani, Christine Chiaverini, Thomas Hubiche, Eric Fontas, Ruxanda Moschoi, Sagair Hussain   +5 more
doaj   +1 more source

Dystrophic epidermolysis bullosa

, 2013
Dystrofische epidermolysis bullosa (DEB) is een erfelijke huidaandoening, veroorzaakt door mutaties in het COL7A1 gen. Bij DEB ontstaan reeds door geringe wrijving blaren van de huid en slijmvliezen. Hoewel bepaalde verbanden tussen het genotype - de COL7A1 mutatie(s) - en het fenotype - de uiting van DEB - bekend zijn, zijn veel aspecten van de ...
openaire   +1 more source

Alterations in Gut Microbiome Diversity and Composition in Patients with Epidermolysis Bullosa: A Case-Control Study

Indian Journal of Dermatology
Epidermolysis bullosa (EB) is a rare inherited genodermatosis that affects both the skin and gastrointestinal tract, potentially leading to altered gut microbiota.
Suci Widhiati, Hardyanto Soebono, Dewajani Purnomosari, Tri Wibawa   +3 more
doaj   +1 more source

Understanding the Pathogenesis of Recessive Dystrophic Epidermolysis Bullosa Squamous Cell Carcinoma

, 2010
Patients with recessive dystrophic epidermolysis bullosa develop numerous life-threatening skin cancers. The reasons for this remain unclear. Parallels exist with other scarring skin conditions, such as Marjolin ulcer.
O'Toole, Edel A., South, Andrew P.
core   +1 more source