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Titlebook: Management of Blistering Diseases; Fenella Wojnarowska,Robert A. Briggaman Book 1990 Springer Science+Business Media Dordrecht 1990 diseas

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41#
發(fā)表于 2025-3-28 15:43:36 | 只看該作者
Diagnosis, diagnostic and research techniquesct the presence or absence of circulating antibodies by the indirect immunofluorescence (IIF) method. The value of positive or negative IF findings is greatly dependent on the reliability, skill and experience of the laboratory staff carrying out these techniques and also on the knowledge of dermatopathology of the observer who reports them.
42#
發(fā)表于 2025-3-28 22:35:15 | 只看該作者
Epidermolysis bullosa acquisitategorization. Through the years, concepts concerning these patients have gradually evolved. Specific diseases that might have been included in EBA as defined above were removed following their recognition.
43#
發(fā)表于 2025-3-29 02:16:41 | 只看該作者
44#
發(fā)表于 2025-3-29 03:22:18 | 只看該作者
45#
發(fā)表于 2025-3-29 09:32:08 | 只看該作者
46#
發(fā)表于 2025-3-29 15:13:32 | 只看該作者
Bullous pemphigoidal basement membrane zone (BMZ). The majority of these patients also have circulating autoantibodies directed against the BMZ of stratified squamous epithelium. Because of these characteristics, BP is felt to be an autoimmune disease in which the cutaneous lesions may result as a consequence of these anti-BMZ antibodies.
47#
發(fā)表于 2025-3-29 18:56:40 | 只看該作者
48#
發(fā)表于 2025-3-29 23:12:38 | 只看該作者
Epidermolysis bullosa dystrophicaand serves as a clinical marker of these diseases. Traditionally, EBD is subdivided into autosomal recessive and autosomal dominant types. Cases of recessively inherited epidermolysis bullosa dystrophica vary significantly in the severity and extent of the disease that they manifest.
49#
發(fā)表于 2025-3-30 02:15:24 | 只看該作者
50#
發(fā)表于 2025-3-30 05:49:30 | 只看該作者
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