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Titlebook: Autoimmune Diseases of the Skin; Pathogenesis, Diagno Michael Hertl Book 2011Latest edition Springer-Verlag Vienna 2011 Autoimmunkrankheite

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楼主: Chylomicron
发表于 2025-3-23 12:26:36 | 显示全部楼层
Christian Knobloch,Hendrik Schröderm have been described, but a unifying pathophysiologic model remains to be tested. The clinician is faced with considerable uncertainty when choosing a treatment modality for LS. Given the benign natural progression of plaque type morphea, treatment with topical modalities such as superpotent cortic
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https://doi.org/10.1007/978-3-658-41813-7known and the pathogenesis only partly understood. Survival has markedly improved over the past two decades, with the 10-year survival rate approaching 80%, although to date with the exception of cyclophosphamide there is no effective disease-modifying treatment of SSc. The introduction of drugs tha
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Tobias Siedersleben,Stefan Hüsig,Sabine Purinical phenotype of LE ranges in continuum from minor cutaneous lesions to life-threatening vital multi organ dysfunction. Throughout this continuum, skin manifestations are variable and common. There is a commonly accepted classification system that divides lesions into LE specific and LE non-speci
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https://doi.org/10.1007/978-3-8349-6823-4glands. In many biopsies from SS patients, dryness of the skin has been associated with lymphocytic infiltrates in the eccrine glands. Similar to SLE patients, antibody and complement fixation is often detected clinically “normal” skin..However, the extent of dryness of the skin and the clinical app
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Holger Fischer,Gunnar Schomakerient if it is due to an IgE-mediated hypersensitive reaction, and will not be considered further. Intermittent urticaria — frequent bouts of unexplained urticaria at intervals of weeks or months — will be discussed here on the same basis as the ordinary presentation of chronic urticaria but may have
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,Abkürzungen, Einheiten und Formelgrössen,se pathophysiologic mechanisms are currently unknown. Lichen planus (LP), the prototype, is an inflammatory disorder with characteristic purple, polygonal, pruritic papules of the skin and may be accompanied by mucosal lesions. There are many similar clinical variants described, ranging from licheno
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