Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Jolanta D. Torzecka"'
Autor:
Zofia Gerlicz-Kowalczuk, Zbigniew Pietrzak, Jolanta D. Torzecka, Anna Woźnicka, Bożena Dziankowska-Bartkowiak
Publikováno v:
Przegląd Dermatologiczny, Vol 103, Iss 6, Pp 465-468 (2016)
Introduction. Acroosteolysis is a recognized, but under-researched and forgotten manifestation of systemic sclerosis (SSc). Objective . To present a case of exuberant acroosteolysis and subcutaneous tissue calcinosis in the course of SSc. Case report
Externí odkaz:
https://doaj.org/article/495e09afd0c24bd78a09a3cddf00dd66
Publikováno v:
Przegląd Dermatologiczny, Vol 103, Iss 5, Pp 409-416 (2016)
Primary perforating dermatoses (PPD) are a group of skin diseases rarely seen in everyday dermatological practice, which includes elastosis perforans serpiginosa, reactive perforating collagenosis, Kyrle disease and perforating folliculitis. These en
Externí odkaz:
https://doaj.org/article/42484c7ba59441c59c3491bb208d0b5a
Autor:
Jolanta D, Torzecka, Joanna, Narbutt, Anna, Sysa-Jedrzejowska, Elzbieta, Waszczykowska, Jolanta, Lukamowicz, Hendri H, Pas
Publikováno v:
Medical science monitor : international medical journal of experimental and clinical research. 9(12)
Pemphigus is a life-threatening, autoimmune blistering disease, mediated by IgG autoantibodies. The aim of our study was to assess the usefulness of a new enzyme-linked immunosorbent assay (ELISA) in detecting circulating pemphigus autoantibodies, an
Publikováno v:
Medical science monitor : international medical journal of experimental and clinical research. 9(1)
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a benign and very rare skin disorder of uncertain etiology. It occurs in both dermal and subcutaneous forms, which are regarded as variants of the same condition. Clinically, it is characterised b