Results 81 to 90 of about 23,997 (201)
Incidence of P200 pemphigoid: A nationwide study
The anti‐LAMB4 cell‐based immunoassay is a new serological technique that is far superior to dermal immunoblotting for detecting autoantibodies directed against the P200 protein. This method allows a re‐evaluation of the incidence of P200 pemphigoid, which appears to be considerably more frequent than epidermolysis bullosa acquisita.
Fabienne Jouen +7 more
wiley +1 more source
Fatal vascular involvement in systemic lupus erythematosus following epidermolysis bullosa acquisita
Epidermolysis bullosa acquisita may be associated with various systemic diseases, including systemic lupus erythematosus. We describe the clinical and immunological findings in a 38-year-old women with epidermolysis bullosa acquisita and systemic lupus ...
이광훈
core +1 more source
Necrotizing fasciitis – a complication of autoimmune skin blistering diseases?
Introduction: Autoimmune bullous diseases (AIBD) are organ-specific skin blistering diseases clinically manifesting as bullae and vesicles of the skin and mucous membranes.
Milana Jurišić +3 more
doaj +1 more source
Expert consensus on oral management in autoimmune bullous diseases, erythema multiforme and SJS/TEN
This international Delphi study achieved expert consensus on 58 statements guiding the management of oral involvement in autoimmune bullous diseases, erythema multiforme and SJS‐TEN. The recommendations emphasize multidisciplinary care, oral hygiene and tailored topical, systemic and inpatient oral management.
Shalini Nayee +39 more
wiley +1 more source
The sera from two patients with epidermolysis bullosa acquisita were blotted against dermal extracts in comparison with the mouse monoclonal antibody LH 7.2. This antibody reacts with carboxy terminal region of type VII collagen.
Whitehead, PC +4 more
core +1 more source
Epidermolysis Bullosa Acquisita
SUMMARYFour patients with the clinical picture of epidermolysis bullosa acquisita were investigated. Biopsies were taken from the involved and uninvolved areas of the skin and the immunohistochemical and microscopic changes were studied. Direct immunofluorescence showed deposition of IgG and C3/4 in a linear or notched pattern along the epidermal ...
C. NIEBOER +3 more
openaire +2 more sources
Periodontitis and Periodontal Conditions in Systemically Healthy Children and Adolescents
ABSTRACT Objective To answer the PICoS question ‘in systemically healthy children and adolescents (Population), what are the main features of periodontitis, necrotising periodontal diseases (NPD) and other periodontal conditions (periodontal abscesses, endo‐periodontal lesions, traumatic occlusal forces, prosthesis‐ and tooth‐related factors ...
Inbar Eshkol‐Yogev +5 more
wiley +1 more source
Epidermolysis bullosa acquisita associated with vitiligo, Graves' disease and nephrotic syndrome
Epidermolysis bullosa acquisita. is a rare autoimmune disease which may be associated with various autoimmune diseases. Presented is an unusual case of a patient with vitiligo, Graves' disease, nephrotic syndrome and epidermolysis bullosa acquisita ...
ERGUN, SAFİYE ATLAS TÜLİN
core +1 more source
Epidermolysis Bullosa Acquisita in Children: Case Series
Background. Epidermolysis bullosa acquisita (EBA) is chronic disease accompanied with subepidermal blistering on skin and mucous membranes as a result of autoimmune aggression to type VII collagen.
Nikolay N. Murashkin +5 more
doaj +1 more source
Multiple milia formation in blistering diseases
Background: Milia are superficial keratinous cysts seen as pearly white, dome-shaped lesions 1–2 mm in diameter. Milia are associated with diseases that cause subepidermal blistering, such as hereditary forms of epidermolysis bullosa, epidermolysis ...
Aikaterini Patsatsi, MD, PhD +2 more
doaj +1 more source

