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Nature Reviews Disease Primers
Bullous pemphigoid is a chronic, subepidermal autoimmune blistering disease characterized by tense blisters on erythematous or normal skin that predominantly affects the older population. The disease arises from autoantibodies targeting hemidesmosomal proteins BP180 and BP230, which are crucial for dermal-epidermal adhesion.
Hossein Akbarialiabad +11 more
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Bullous pemphigoid is a chronic, subepidermal autoimmune blistering disease characterized by tense blisters on erythematous or normal skin that predominantly affects the older population. The disease arises from autoantibodies targeting hemidesmosomal proteins BP180 and BP230, which are crucial for dermal-epidermal adhesion.
Hossein Akbarialiabad +11 more
+7 more sources
Journal of dermatology (Print), 2023
Biological drugs, including IL‐17A inhibitors, have become the first‐line treating options for moderate to severe psoriasis, and reports show a beneficial effect of IL‐17A inhibitors on bullous pemphigoid.
Rui Wang, Aiping Wang, Mingyue Wang
semanticscholar +1 more source
Biological drugs, including IL‐17A inhibitors, have become the first‐line treating options for moderate to severe psoriasis, and reports show a beneficial effect of IL‐17A inhibitors on bullous pemphigoid.
Rui Wang, Aiping Wang, Mingyue Wang
semanticscholar +1 more source
European Journal of Dermatology, 2022
Bullous pemphigoid (BP) is relatively rare in the paediatric age group, with slightly more than 100 cases of BP reported in the literature. In this article, we focus on infantile BP (>= 28 days, <12 months), presenting a systematic review of cases of infantile BP in the literature from 1977 up to the present day. Fifty-four articles were selected,
Cozzani, Emanuele +4 more
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Bullous pemphigoid (BP) is relatively rare in the paediatric age group, with slightly more than 100 cases of BP reported in the literature. In this article, we focus on infantile BP (>= 28 days, <12 months), presenting a systematic review of cases of infantile BP in the literature from 1977 up to the present day. Fifty-four articles were selected,
Cozzani, Emanuele +4 more
openaire +2 more sources
Global incidence and prevalence of bullous pemphigoid: A systematic review and meta‐analysis
Journal of Cosmetic Dermatology, 2022Integrated information on the global prevalence and incidence of bullous pemphigoid (BP) is lacking.
Lingling Lu +3 more
semanticscholar +1 more source
Autoimmunity Reviews, 2017
Bullous pemphigoid (BP) is the most common autoimmune bullous disorder which is characterized by autoantibodies against hemidesmosomal proteins of the skin and mucous membranes. Collagen XVII and dystonin-e have been identified as target antigens. BP affects mostly the elderly. The incidence of the disease is increasing gradually and is associated with
Işın Sinem, Bağcı +3 more
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Bullous pemphigoid (BP) is the most common autoimmune bullous disorder which is characterized by autoantibodies against hemidesmosomal proteins of the skin and mucous membranes. Collagen XVII and dystonin-e have been identified as target antigens. BP affects mostly the elderly. The incidence of the disease is increasing gradually and is associated with
Işın Sinem, Bağcı +3 more
openaire +3 more sources
Dermatologic Clinics, 1987
Bullous pemphigoid is an acquired subepidermal blistering disease of the elderly characterized by tense blisters. Patients with bullous pemphigoid have circulating and tissue-bound antibodies that are directed against a normal component of the epidermal basement membrane.
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Bullous pemphigoid is an acquired subepidermal blistering disease of the elderly characterized by tense blisters. Patients with bullous pemphigoid have circulating and tissue-bound antibodies that are directed against a normal component of the epidermal basement membrane.
openaire +5 more sources
International Journal of Dermatology, 1992
AbstractThree patients had a rare form of bullous pemphigoid, clinically similar to the erythematous type of bullous pemphigoid without vesiculobullous lesions. All the patients displayed immunofluorescence features of bullous pemphigoid. This form of the disease presents a substantial diagnostic problem because it lacks the principal morphologic ...
R, Wolf, J, Ophir, E, Dechner
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AbstractThree patients had a rare form of bullous pemphigoid, clinically similar to the erythematous type of bullous pemphigoid without vesiculobullous lesions. All the patients displayed immunofluorescence features of bullous pemphigoid. This form of the disease presents a substantial diagnostic problem because it lacks the principal morphologic ...
R, Wolf, J, Ophir, E, Dechner
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Erythrodermic bullous pemphigoid
Journal of the American Academy of Dermatology, 1993REFERENCES L Korman N, Pemphigus. J AM ACAD DERMATOL 1988; 18:1219-38. 2. Barthelemy H, Frappaz A, Cambazard F, et al. Treatment of nine cases of pemphigus vulgaris with cyclosporine. J AM ACAD DERMATOL 1988;18:1262-6, 3. ~evuz J. Plasmapheresis. In: Orfanos CE, Stadler R, GollDIck H, eds. Dermatology in five continents.
A, Saitoh +5 more
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The American Journal of Dermatopathology, 2015
Rare clinical variants of bullous pemphigoid (BP) include vesicular BP, dyshidrosiform BP, pemphigoid nodularis, seborrheic BP, pemphigoid vegetans, localized BP, erythrodermic BP, and juvenile BP. To our knowledge, this is the first report of an unusual case of purpuric BP. We present a case of 85-year-old white man who presented with a 2-week history
Maruska, Marovt +1 more
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Rare clinical variants of bullous pemphigoid (BP) include vesicular BP, dyshidrosiform BP, pemphigoid nodularis, seborrheic BP, pemphigoid vegetans, localized BP, erythrodermic BP, and juvenile BP. To our knowledge, this is the first report of an unusual case of purpuric BP. We present a case of 85-year-old white man who presented with a 2-week history
Maruska, Marovt +1 more
openaire +2 more sources
International Journal of Dermatology, 2006
AbstractBackground Prodromal bullous pemphigoid (PBP) can be difficult to diagnose. Early recognition in its early stages may decrease the morbidity and progression of the disease. Clinical presentations and current treatments available for PBP will be described.Methods A retrospective review was performed on 53 patients diagnosed with PBP.Results ...
Philina M, Lamb +4 more
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AbstractBackground Prodromal bullous pemphigoid (PBP) can be difficult to diagnose. Early recognition in its early stages may decrease the morbidity and progression of the disease. Clinical presentations and current treatments available for PBP will be described.Methods A retrospective review was performed on 53 patients diagnosed with PBP.Results ...
Philina M, Lamb +4 more
openaire +2 more sources