نتایج جستجو برای: kindler
تعداد نتایج: 219 فیلتر نتایج به سال:
We address cross-organizational workflows, such as document workflows, which consist of multiple workflow modules each of which can interact with others by sending and receiving messages. Our goal is to guarantee that the global workflow network has properties such as termination while merely requiring properties that can be checked locally in individual modules. The resulting query nets are ba...
BACKGROUND Kindler Syndrome (KS) is an autosomal recessive skin disorder characterized by skin blistering, photosensitivity, premature aging, and propensity to skin cancer. In spite of the knowledge underlying cause of this disease involving mutations of FERMT1 (fermitin family member 1), and efforts to characterize genotype-phenotype correlations, the clinical variability of this genodermatosi...
Epidermolysis bullosa (EB) is a group of inherited blistering skin diseases that vary widely in their pathogenesis and severity. It has been divided into distinct subtypes depending on the level of tissue separation in the dermal- epidermal basement membrane zone. There are four main categories of EB: simplex, junctional, dystrophic and Kindler syndrome. Junctional epidermolysis bullosa with py...
M. Schädel, D. Ackermann, W. Brüchle, Ch.E. Düllmann, J. Dvorak, K. Eberhardt, J. Even, A. Gorshkov, R. Gräger, K.E. Gregorich, F.P. Heßberger, A. Hübner, E. Jäger, J. Khuyagbaatar, B. Kindler, J.V. Kratz, D. Liebe, B. Lommel, J.P. Omtvedt, K. Opel, A. Sabelnikov, F. Samadani, B. Schausten, R. Schuber, E. Schimpf, A. Semchenkov, J. Steiner, J. Szerypo, A. Türler, and A. Yakushev for the TASCA C...
Kindler syndrome (KS) is a rare, autosomal recessive genodermatosis characterized by skin blistering and photosensitivity in infancy, progressive poikiloderma, and diffuse cutaneous atrophy. It affects the skin, mucous membranes, and oral cavity and is caused by mutations in the KIND1 gene on 20p12.3. The first case of KS associated with periodontitis was reported in 1996, and have been infrequ...
Kindler syndrome (KS) is a rare autosomal recessive genodermatosis. We report two cases of KS with classical clinical presentations involving skin and mucus membranes. Clinically, both patients had four major features of KS in the form of acral skin blistering, photosensitivity, progressive poikiloderma, and diffuse cutaneous atrophy. Case 1 had associated features in the form of urethral...
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