Results 71 to 80 of about 2,889 (186)

Hemidesmosome Mutations Contribute to the Onset and Severity of Acquired Autoimmune Bullous Diseases

open access: yesMedComm, Volume 7, Issue 3, March 2026.
This study examined hemidesmosome assembly‐related genes in pemphigoid diseases, revealing variants linked to disease onset and severity. Functional analyses, including Caenorhabditis elegans models, Ker‐CT transcriptomics, human proteomics, etc., demonstrated that ITGA6 mutations destabilize hemidesmosomes, disrupt dermal–epidermal adhesion, and ...
Shan Cao   +19 more
wiley   +1 more source

A Case of Bullous Skin Disease Presenting with Odynophagia: A Diagnostic Challenge

open access: yesCase Reports in Dermatological Medicine, 2016
We report a case of Epidermolysis Bullosa Acquisita (EBA) that presented as a diagnostic challenge. A 60-year-old Qatari lady presented with odynophagia, oral ulceration, and weight loss.
G. Kravvas, D. Veitch, C. M. Perrett
doaj   +1 more source

Risk of persistent hypogammaglobulinaemia in children with autoimmune bullous dermatoses treated with rituximab

open access: yes
Journal of the European Academy of Dermatology and Venereology, EarlyView.
S. Benkimoun   +14 more
wiley   +1 more source

Noninvasive Imaging Techniques as Modern Diagnostic Tools in Desquamative Gingivitis: Focus on RCM, OCT, and LC‐OCT

open access: yesSkin Research and Technology, Volume 32, Issue 1, January 2026.
ABSTRACT Background Desquamative gingivitis is a clinical condition characterized by erythema, blisters, and erosions within the gingiva. It may be a manifestation of oral lichen planus or autoimmune bullous diseases, such as pemphigus vulgaris and mucous membrane pemphigoid. The identification of the cause of desquamative gingivitis typically involves
Urszula Fałkowska   +7 more
wiley   +1 more source

Epidermolysis Bullosa Acquisita - A Case Report

open access: yesIndian Journal of Dermatology, 2002
A 50 year old lady presented with multiple pruritic fluid filled lesions all over the body of 5 years duration. Lesions healed with scarring and milia. Immunofluroescence confirmed the diagnosis of epidermolysis bullosa acquisita.
Feranandes Carol Z, Bhat M Ramesh
doaj  

Pyoderma Gangrenosum as the First Manifestation of Inflammatory Bowel Disease: A Case Report

open access: yesCase Reports in Gastrointestinal Medicine, Volume 2026, Issue 1, 2026.
Approximately 50% of patients with inflammatory bowel disease (IBD) exhibit extraintestinal manifestations, among which skin and mucosal lesions are common. However, pyoderma gangrenosum occurs in only 1%‐2% of IBD patients. We report the case of a 23‐year‐old male patient who was admitted to the hospital with pyoderma gangrenosum that was unresponsive
Nam Hoai Nguyen   +7 more
wiley   +1 more source

Progressive Linear Bullous Eruption in a Young Athlete: A Diagnostic Challenge

open access: yes
Journal of Paediatrics and Child Health, EarlyView.
Chon‐Wai Jeremy Chan   +4 more
wiley   +1 more source

ROS‐Scavenging Multifunctional Microneedle Patch Facilitating Wound Healing

open access: yesAdvanced Healthcare Materials, Volume 14, Issue 31, December 8, 2025.
A reactive oxygen species (ROS) scavenging and immunomodulatory microneedle patch based on hyaluronic acid methacrylate (HaMA) and Flightless I (Flii)‐siRNA‐laden arginine functionalized poly (β‐amino ester)/alginate particles is developed for chronic wound healing applications.
Mahshid Kharaziha   +4 more
wiley   +1 more source

Epidermolysis Bullosa Acquisita Mimicking Linear IgA Bullous Disease in a 5-year-old Child [PDF]

open access: yes, 2020
We present a case of a 5-year-old child with epidermolysis bullosa acquisita, clinically resembling linear IgA bullous disease. The case demonstrates that autoimmune bullous dermatoses in childhood may show a clinical overlap, which makes the diagnosis ...
Grisha Mateev   +4 more
core   +2 more sources

Paraneoplastic epidermolysis bullosa acquisita associated with thyroid carcinoma [PDF]

open access: yes, 2016
n/
Alessandro Monopoli   +8 more
core   +1 more source

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