Results 41 to 50 of about 1,324,064 (165)
Management of Mucous Membrane Pemphigoid [PDF]
Mucous membrane pemphigoid (MMP) is a chronic autoimmune subepithelial vesiculobullousdisorder predominantly affects the mucous membranes more frequently than the skin. Several targetantigens in basement membrane zone have been identified in MMP.
Sanguansin, Nutchaporn +1 more
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Analgesic effects of platelet‐rich fibrin (PRF): A systematic review
Abstract Background Platelet‐rich fibrin (PRF), a second‐generation autologous platelet concentrate, has gained significant interest for its anti‐inflammatory and regenerative characteristics. While its role in tissue healing is well‐recognized, the analgesic potential of PRF remains under‐investigated.
Nathan E. Estrin +6 more
wiley +1 more source
Mucous Membrane Pemphigoid-Immunofluorescent Studies
Mucous membrane pemphigoid differs from pemphigus vulgaris or bullous pemphigoid in clinical course, response to steroid therapy, and absence of characteristic antibodies.
Harvey A. Brody, Kirk D. Wuepper
core +1 more source
Mucous membrane pemphigoid is an autoimmune blistering disorder characterized by predominant involvement of surface-close epithelia and linear depositions of immunoreactants at the dermal-epithelial junction on direct immunofluorescence microscopy.
Kaan Yilmaz +6 more
core +1 more source
Increasing Prevalence of Syphilis: Oral Manifestations, Diagnosis and Management
ABSTRACT Introduction Cases of syphilis are increasing, with 9513 cases diagnosed in England in 2023, the highest annual number since 1948. Oral healthcare professionals should therefore be aware of how oral syphilis presents, the differential diagnosis and the appropriate care pathway and management.
C. C. Currie +8 more
wiley +1 more source
Treatment strategies in mucous membrane pemphigoid
Ann G Neff, Matthew Turner, Diya F MutasimDepartment of Dermatology, University of Cincinnati, Cincinnati, OH, USAAbstract: Mucous membrane pemphigoid (MMP) is an autoimmune blistering disorder that is characterized by subepithelial bullae.
Diya F Mutasim +2 more
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Systematic Review of Management Strategies for Alport Syndrome: Implications for Male Patients
ABSTRACT Background and Aims Alport Syndrome (AS) is a rare genetic disorder characterized by progressive kidney disease, hearing loss, and ocular abnormalities, with an incidence of approximately 1 in 50,000 newborns. Due to the severity of the disease, particularly in males with X‐linked inheritance, this systematic review consolidates current ...
Zouina Sarfraz +10 more
wiley +1 more source
Benign mucous membrane pemphigoid--a case report.
Benign mucous membrane pemphigoid (BMMP) is a relatively rare, chronic vesiculobullous disease. It frequently affects postmenopausal women, although cases have been reported in younger individuals.
Naidoo S., Puranwasi R.
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Biologic Treatment Outcomes in Mucous Membrane Pemphigoid: A Systematic Review
JAAD - Supplementary Files and Table for "Biologic Treatment Outcomes in Mucous Membrane Pemphigoid: A Systematic ...
Lytvyn, Y (via Mendeley Data)
core +1 more source
Diagnostic challenge: Juvenile bullous pemphigoid with a negative BP180 ELISA
Abstract Bullous pemphigoid (BP) is an autoimmune blistering disease primarily affecting the elderly, whereas cases of juvenile BP are rare. Both types of BP are typically mediated by autoantibodies targeting the NC16A region of BP180; however, a small subset of adult patient sera react to other regions of the protein.
Janet A. Fairley +4 more
wiley +1 more source

