Results 41 to 50 of about 2,851 (167)
Acta Dermato-Venereologica, 2018 Circulating anti-type VII collagen autoantibodies are frequently detected in patients with recessive dystrophic epidermolysis bullosa (RDEB). However, evidence supporting their pathogenic role in inducing epidermolysis bullosa acquisita (EBA) has been ...
Liliana Guerra +6 more
doaj +1 more source
Anais Brasileiros de Dermatologia, 2009 Apresenta-se caso de epidermólise bolhosa adquirida inflamatória. Paciente do sexo masculino, 53 anos, há seis meses com erupção vesicobolhosa pruriginosa sobre base eritematosa no tronco, axilas e membros.
Marcelo D'Ambrosio Fernandes +4 more
doaj +1 more source
EndoS reduces the pathogenicity of anti-mCOL7 IgG through reduced binding of immune complexes to neutrophils. [PDF]
PLoS ONE, 2014 Endo-β-N-acetylglucosaminidase (EndoS) has been shown to act as a potent pathogen-derived immunomodulatory molecule in autoimmune diseases. Here we investigated how EndoS treatment reduces the pathogenicity of rabbit anti-mCOL7 IgG using different ...
Xinhua Yu +5 more
doaj +1 more source
Clinical Dermatology Review, 2020 We describe a female child in the first decade patient admitted to a children's hospital for lip swelling and constipation who was ultimately diagnosed with Crohn's disease.
Maggie L Chow, Minnelly Luu
doaj +1 more source
Angina bullosa hemorrhagica an enigmatic oral disease [PDF]
, 2015 Angina bullosa hemorrhagica (ABH) is an enigmatic oral disorder described for the first time by Badham in 1967 to define blisters with a hematic content in the oral cavity and oropharynx unrelated to any hematological, dermatological or systemic ...
Aguirre-Urizar, Jose Manuel +3 more
core +1 more source
Epidermolysis Bullosa Acquisita Occuring In A Patient With Systemic Lupus Erythematosus
Saintika Medika, 2019 Epidermolysis Bullosa Acquisita (EBA) is a rare, chronic autoimmune subepidermal bullous disease and has been noted to be associated with systemic lupus erythematosus (SLE). The incidence of EBA and SLE in one patient within the period of 1980-1990 found
Lita setyowatie +3 more
doaj +1 more source
Bullous Pemphigoid and Other Pemphigoid Dermatoses
Medicina, 2021 The pemphigoid family of dermatoses is characterized by autoimmune subepidermal blistering. The classic paradigm for pemphigoid, and the most common member, is bullous pemphigoid.
Valeryia Pratasava +6 more
doaj +1 more source
Acquired Epidermolysis Bullosa and Linear Immunoglobulin A Bullous Dermatosis [PDF]
, 2017 Acquired epidermolysis bullosa is a rare subepidermal bullous disease characterized by autoantibodies to type VII collagen, the major component of anchoring fibrils. Although the exact pathophysiologic mechanism remains unclear, reduction or perturbation
Atay, Seda, Çelik, Gökçen
core +1 more source
Journal of the Egyptian Women’s Dermatologic SocietyEpidermolysis Bullosa Acquisita is a rare, chronic autoimmune blistering disorder characterized by vesicles and bullae on the skin and mucous membranes.
Fahad Alrashidi +2 more
doaj +1 more source