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The Role of Microbiota in the Pathogenesis of Bullous Pemphigoid and Pemphigus Vulgaris: Evidence, Controversies, and Perspectives. [PDF]

Int J Mol Sci
Gorini F, Coi A, Santoro M, Tonacci A, Sansone F, Mariotti EB, Donati M, Verdelli A, Nasca MR, Amerio P, Antiga E, Barletta E, Caproni M.   +12 more
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Treatment of Bullous Pemphigoid

The Journal of Dermatology, 2003
AbstractBullous pemphigoid (BP) is the most frequent auto‐immune blistering skin disease. Up to recently, it was treated with oral corticosteroids. High dose steroids are poorly tolerated in the elderly and probably contributed to the high mortality rates observed in several cohorts.
Pascal Joly, Pascal Joly, Jean-Claude Roujeau, Juliette Fontaine   +3 more
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Erythrodermic bullous pemphigoid [PDF]

Journal of the American Academy of Dermatology, 1993
REFERENCES 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.
Yasuo Kubota, Kunihiko Tamaki, Atsushi Saitoh, Naoto Ohtake, Atsushi Osada, Shinji Shimada   +5 more
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BULLOUS PEMPHIGOID IN AN ABORIGINE

Australasian Journal of Dermatology, 1993
SummaryObjective: To present the first case of bullous pemphigoid in an Australian Aborigine.Clinical features: A 47 year old female aborigine presented with a three week history of a generalised skin eruption consistent with bullous pemphigoid. Immunohistological examination confirmed the diagnosis.
Sydney Lo, Ajay Kumar, Lindsay C. Mollison   +2 more
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NONBULLOUS BULLOUS PEMPHIGOID

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 ...
Ronni Wolf, Edit Dechner, Joseph Ophir
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Erythrodermic bullous pemphigoid

International Journal of Dermatology, 2001
Case 1 An 87‐year‐old man, with a 2‐year history of a generalized exfoliative erythroderma involving approximately 90% of the body, presented with an onset of tense blisters symmetrically distributed on most of his body.Clinical examination revealed generalized erythema, edema, moderate lichenification, and scaling, with several tense and grouped ...
L. Amato, I. Gallerani, S. Mei, E. Perrella, M. Caproni, FABBRI, PAOLO   +5 more
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Bullous pemphigoid in adolescence

Pediatric Dermatology, 2018
AbstractBullous pemphigoid (BP) is the most common autoimmune blistering disease affecting the elderly but is quite rare in childhood. The majority of pediatric cases have been reported during early childhood. Adolescence is divided into three phases: early (10‐13 years), middle (14‐17), and late (18‐21).
Aikaterini Patsatsi, Aikaterini Kyriakou, Victoria P. Werth   +2 more
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The immunopathology of bullous pemphigoid

Clinics in Dermatology, 1987
Abstract The immunopathology of bullous pemphigoid features basement membrane zone (BMZ) deposition of immunoglobulin and complement and the presence of circulating immunoreactants. 1,2 The demonstration of linear subepidermal deposition of C3 and/or IgG is usually necessary to establish the diagnosis.
Robert E. Jordon, Robert E. Jordon, Michael J. Imber, Michael J. Imber, George F. Murphy, George F. Murphy   +5 more
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Bullous and cicatricial pemphigoid

Journal of Autoimmunity, 1991
Bullous pemphigoid (BP) and cicatricial pemphigoid are blistering mucocutaneous diseases characterized by detachment of the overlying epithelium from its stroma. IgG and complement components are deposited in all affected tissue at the level of blister formation--through the lamina lucida of the epithelium. The primary antibody response is of the IgG 4
Lynne H. Morrison, Grant J. Anhalt
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Bullous pemphigoid in an infant

Australasian Journal of Dermatology, 1995
SUMMARYAn acral blistering eruption in a 10 week old baby was found on histology and direct immunofluorescence to be bullous pemphigoid. Circulating auto‐antibodies were not detected. He responded quickly to oral prednisolone and there have been no sequelae.
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