Zobrazeno 1 - 10 of 58 pro vyhledávání: '"DIF, direct immunofluorescence"'
3
Bullous eczema presenting as bullous pemphigoid-like eruption: A case series
Autor: George Atteh, Emily F. Cole, Adam J Perricone, Ron J. Feldman
Publikováno v: JAAD Case Reports, Vol 10, Iss, Pp 34-37 (2021)
JAAD Case Reports
Bullous pemphigoid (BP) is an autoimmune blistering disease resulting from autoantibodies directed against BP180 and/or BP230 proteins. BP is traditionally diagnosed based on clinical features, histologic assessment of cutaneous biopsies, direct (DIF
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dc0ef059fe2ded020fba49107cd9e35
http://www.sciencedirect.com/science/article/pii/S2352512621000886
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5
An atypical case of pediatric epidermolysis bullosa acquisita: Review of diagnosis and pitfalls
Autor: Leah Lalor, Karolyn A. Wanat, Ashaki Patel
Publikováno v: JAAD Case Reports, Vol 9, Iss, Pp 81-85 (2021)
JAAD Case Reports
Epidermolysis bullosa acquisita (EBA) is a rare autoimmune blistering disorder, with
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abf5669fb67abb90835b8b5d10de3b7a
http://www.sciencedirect.com/science/article/pii/S235251262100031X
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6
Mucosal linear IgA disease with esophageal involvement responsive to ustekinumab
Autor: Kristin M. Leiferman, Danny Varedi, Christina Topham, Amber Jimenez, Christopher M. Hull
Publikováno v: JAAD Case Reports
JAAD Case Reports, Vol 15, Iss, Pp 4-6 (2021)
Linear IgA bullous dermatosis (LABD), or linear IgA disease, is a rare autoimmune mucocutaneous blistering disease with vesicles and bullae characteristically arranged in an annular or arciform pattern on the skin and, less common, mucosal involvemen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9965a1a0550cbfcee027bb6705b535c
http://europepmc.org/articles/PMC8340047
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9
Increasing evidence for omalizumab in the treatment of bullous pemphigoid
Autor: Vanessa Holland, Nirali Patel, Suzanne M. Sachsman, Sarah Lonowski, Allison K Truong
Publikováno v: JAAD Case Reports, Vol 6, Iss 3, Pp 228-233 (2020)
JAAD Case Reports
Bullous pemphigoid (BP) is an acquired autoimmune blistering disease characterized by the formation of autoantibodies against hemidesmosomal antigens BP180 and BP230. Although IgG autoantibodies predominate within the plasma and skin of BP patients,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e652ada7c635d6dc524ba9510bcb347e
http://www.sciencedirect.com/science/article/pii/S2352512620300060
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Plný text Recenzováno Digitální knihovna AV ČR
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