Results 91 to 100 of about 4,291 (203)
Proteomic identification of salivary biomarkers in 20 patients with Oral Squamous Cell Carcinoma [PDF]
, 2014 Objectives. Saliva has been proposed as a potential diagnostic fluid combined with proteomic analysis. The aim of this study is to assess the proteomic salivary profile using SELDI-TOF-MS technology in patients with Oral Squamous Cell Carcinoma (OSCC ...
CAMPISI, Giuseppina +3 more
core
Субэпидермальные буллезные дерматозы [PDF]
, 2019 ПЕМФИГОИД БУЛЛЕЗНЫЙПЕМФИГОИД СЛИЗИСТЫХ ОБОЛОЧЕКПРИОБРЕТЕННЫЙ БУЛЛЕЗНЫЙ ЭПИДЕРМОЛИЗДИАГНОСТИКА ДИФФЕРЕНЦИАЛЬНАЯВо второй части статьи, посвященной дерматозам с субэпидермальным расположением пузырей при гистологическом исследовании, описываются буллезный ...
Катина, М. А. +1 more
core +2 more sources
A Rare Type of Bullous Disorder in a Child. Can It Be Chronic Bullous Disease of Childhood?
Clinical Case Reports, Volume 14, Issue 1, January 2026.ABSTRACT Chronic bullous disease of childhood (CBDC), also known as childhood linear IgA bullous dermatosis, is a rare autoimmune disorder characterized by sub‐epidermal blistering and linear deposition of immunoglobulin A at the demo‐epidermal junction.
Rajeev Yadav +3 more
wiley +1 more source
The 'Spectraplakins': cytoskeletal giants with characteristics of both spectrin and plakin families [PDF]
, 2002 Recent studies have characterised a family of giant cytoskeletal crosslinkers encoded by the short stop gene in Drosophila and the dystonin/BPAG1 and MACF1 genes in mammals.
Brown, N., Gregory, S., Roeper, K.
core +2 more sources
Epiglottic Ulceration as an Initial Manifestation of Crohn's Disease
Journal of General and Family Medicine, Volume 27, Issue 1, January 2026.ABSTRACT Crohn's disease can present with various extraintestinal symptoms; however, laryngeal involvement, particularly epiglottic ulcers, is rare. A 52‐year‐old man presented with a sore throat. Laryngeal endoscopy revealed an epiglottic ulcer. He had no gastrointestinal symptoms.
Niina Yamashita +2 more
wiley +1 more source
Case Reports in Dermatology, 2013 Lichen planus pemphigoides (LPP) is a rare clinical variant of bullous pemphigoid (BP). A 35-year-old female patient presented to our hospital complaining of pruritic violaceous-colored plaques or papules on the extremities. Tense vesicles were also seen
Ken Washio +4 more
doaj +1 more source
Tight Clustering of Extracellular BP180 Epitopes Recognized by Bullous Pemphigoid Autoantibodies
Journal of Investigative Dermatology, 1997 Bullous pemphigoid is a blistering skin disease associated with autoantibodies against the BP180 antigen, a transmembrane component of the hemidesmosome. Anti-BP180 antibodies have been demonstrated to be pathogenic in a passive transfer mouse model.
Zillikens, Detlef +6 more
openaire +2 more sources
Gliptin Accountability in Mucous Membrane Pemphigoid Induction in 24 Out of 313 Patients
Frontiers in Immunology, 2018 Mucous membrane pemphigoids (MMPs) and bullous pemphigoid (BP) are autoimmune bullous diseases that share physiopathological features: both can result from autoantibodies directed against BP180 or BP230 antigens.
Olivier Gaudin +14 more
doaj +1 more source
Financing the U.S. Health System: Issues and Options for Change [PDF]
, 2008 Explores key issues of health reform and options for financing health care -- redirecting funds to more effective uses, rolling back tax cuts, modifying tax exclusions for health benefits, an employer play-or-pay model, and a value-added ...
Jeanne M. Lambrew +2 more
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Paraneoplastic pemphigus: insight into the autoimmune pathogenesis, clinical features and therapy [PDF]
, 2017 Paraneoplastic pemphigus is a rare autoimmune skin disease that is always associated with a neoplasm. Usually, oral, skin, and mucosal lesions are the earliest manifestations shown by paraneoplastic pemphigus patients.
Andrea Ciofalo +21 more
core +2 more sources