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The Global Incidence Rate of Pemphigus Vulgaris: A Systematic Review and Meta-Analysis
Dermatology, 2023Background: Pemphigus vulgaris is a life-threatening autoimmune bullous disease characterized by flaccid blister formation. As there has been no macroscopic assessment of epidemiological characteristics, its disease burden in the general population ...
Liujie Zhao, Yan Chen, Mingyue Wang
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A case report of the beneficial effect of oclacitinib in a dog with pemphigus vulgaris.
Veterinary dermatology (Print), 2022Pemphigus vulgaris is a rare immune-mediated skin disorder of the dog, usually treated with immunosuppressive medications such as oral glucocorticoids, azathioprine or ciclosporin. Herein we report the successful treatment of pemphigus vulgaris in a dog,
N. Martinez, Beth McDonald, A. Crowley
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Oral Diseases, 2021
Pemphigus vulgaris is an autoimmune blistering disease with an increased potential for mortality. The epithelium is key in understanding the pathobiology as it is specialized to perform functions like mechanical protection, immunological defense, and ...
H. R+5 more
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Pemphigus vulgaris is an autoimmune blistering disease with an increased potential for mortality. The epithelium is key in understanding the pathobiology as it is specialized to perform functions like mechanical protection, immunological defense, and ...
H. R+5 more
semanticscholar +1 more source
British Journal of Dermatology, 2020
Acantholysis in pemphigus vulgaris (PV) may be triggered by desmoglein (Dsg) and non‐Dsg autoantibodies. The autoantibody profile of each patient results in distinct intracellular signalling patterns.
M. Ivars+5 more
semanticscholar +1 more source
Acantholysis in pemphigus vulgaris (PV) may be triggered by desmoglein (Dsg) and non‐Dsg autoantibodies. The autoantibody profile of each patient results in distinct intracellular signalling patterns.
M. Ivars+5 more
semanticscholar +1 more source
Pemphigus Vulgaris and Paraneoplastic Pemphigus
Oral and Maxillofacial Surgery Clinics of North America, 2008The history, epidemiology, pathophysiology, clinical presentation, diagnostic work-up, histopathology, and treatment of PV and PNP have been presented. These life-threatening, autoimmune, mucocutaneous bullous conditions may be encountered first by oral health providers and, therefore, deserve keen understanding and attention by the oral and ...
Ronald E. Grimwood+2 more
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The Journal of the American Dental Association, 1980
Pemphigus vulgaris is a rare, potentially fatal skin disease with lesions usually first appearing in the mouth. Histologic examination is the only reliable mechanism with which to establish an accurate diagnosis. An elderly patient with multiple oral and skin lesions was diagnosed, referred to the dermatology service, and successfully treated with ...
P L, Kempler, T R, Schott
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Pemphigus vulgaris is a rare, potentially fatal skin disease with lesions usually first appearing in the mouth. Histologic examination is the only reliable mechanism with which to establish an accurate diagnosis. An elderly patient with multiple oral and skin lesions was diagnosed, referred to the dermatology service, and successfully treated with ...
P L, Kempler, T R, Schott
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Etanercept for pemphigus vulgaris
Italian Journal of Dermatology and Venereology, 2019N ...
Savoia, Francesco+5 more
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Acta Paediatrica, 1991
ABSTRACT. Pemphigus vulgaris is extremely rare in childhood. Only 35 cases of juvenile pemphigus vulgaris have been reported in the literature up until to now. During the pre‐steroid era, the outcome of the disease was usually regarded as fatal. Today, the prognosis has improved because of the possibility of early diagnosis by immunoflourescent ...
V. Graff-Lonnevig, T. Kaaman
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ABSTRACT. Pemphigus vulgaris is extremely rare in childhood. Only 35 cases of juvenile pemphigus vulgaris have been reported in the literature up until to now. During the pre‐steroid era, the outcome of the disease was usually regarded as fatal. Today, the prognosis has improved because of the possibility of early diagnosis by immunoflourescent ...
V. Graff-Lonnevig, T. Kaaman
openaire +3 more sources
Journal of the American Academy of Dermatology, 1982
An infant was born with bullous lesions. The mother had had pemphigus vegetans diagnosed 1 year earlier, with remission during pregnancy. Histopathology and immunofluorescence of the infant's lesions were consistent with pemphigus vulgaris. The mother and infant had low titers of epidermal intercellular antibodies in their sera.
Wesley K. Galen+3 more
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An infant was born with bullous lesions. The mother had had pemphigus vegetans diagnosed 1 year earlier, with remission during pregnancy. Histopathology and immunofluorescence of the infant's lesions were consistent with pemphigus vulgaris. The mother and infant had low titers of epidermal intercellular antibodies in their sera.
Wesley K. Galen+3 more
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Oesophageal Pemphigus vulgaris
Dermatology, 1988Symptomatic involvement of the oesophageal mucosa by pemphigus vulgaris is rare. We describe 1 patient who was treated with oral steroids during a blistering phase, when epigastric pain developed. Endoscopy revealed multiple ulcerations all over the oesophagus, but gastroduodenal mucosa was normal.
Peter Coode+3 more
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