Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Marwah A, Saleh"'
Autor:
Galal El Enany, Noha Nagui, Hanan Nada, Marwa M Fawzy, Marwah A Saleh, Iman Sany, Ahmad Nada, Mona Korany, Omar El Ghanam
Publikováno v:
Journal of the Egyptian Women’s Dermatologic Society, Vol 18, Iss 1, Pp 75-78 (2021)
Epidermolysis bullosa acquisita (EBA) is a chronic autoimmune subepidermal blistering disease of the skin and mucous membranes. EBA is caused by antibodies targeting type VII collagen, the major component of anchoring fibrils that connects the baseme
Externí odkaz:
https://doaj.org/article/cff07fcb31c343818fa7f35478780663
Publikováno v:
Journal of the Egyptian Women’s Dermatologic Society, Vol 17, Iss 1, Pp 31-37 (2020)
Background Although the exact pathogenic mechanisms leading to blister formation in pemphigus vulgaris (PV) have not been fully elucidated, intracellular signaling following antibody binding has been found to be necessary for inducing cell-cell disso
Externí odkaz:
https://doaj.org/article/9605e347cb2346509ee0db9909dfae7c
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 94, Iss 4, Pp 399-404 (2019)
Abstract: Background: The Autoimmune Bullous Disease Quality of Life (ABQOL) and the Treatment of Autoimmune Bullous Disease Quality of Life (TABQOL) questionnaires proved to be reliable tools that measure the disease and treatment burden. Objectives
Externí odkaz:
https://doaj.org/article/845ec59ac4c248dd9ba6252e505c37b2
Publikováno v:
Indian Journal of Dermatology, Vol 62, Iss 1, Pp 47-51 (2017)
Background: Pemphigus vulgaris (PV) is an immunoglobulin G-mediated autoimmune bullous skin disease. Nonorgan-specific antibodies were detected in Tunisian and Brazilian pemphigus patients with different prevalence. Materials and Methods: Fifty PV pa
Externí odkaz:
https://doaj.org/article/0a4b8b6deda5485782790c6c828fd4f5
Autor:
Manal Bosseila, Eman A. Nabarawy, Mostafa A. Latif, Sally Doss, Mona ElKalioby, Marwah A Saleh
Publikováno v:
Dermatology Practical & Conceptual, Vol 9, Iss 2 (2019)
Externí odkaz:
https://doaj.org/article/56f8d28036c34d0c8a2fbb0149ed32fe
Publikováno v:
Wound Repair and Regeneration. 30:448-452
Pemphigus vulgaris (PV) is an autoimmune bullous skin disease. Aquaporin 3 (AQP3) is a glycerol/water channel involved in several physiological functions. Evaluation of the tissue expression and localization of AQP3 in the skin of PV patients. Twenty
Publikováno v:
Archives of Dermatological Research. 315:61-66
Morphea is an inflammatory fibrosing disease, initiated by vascular injury resulting in increased collagen formation and decreased collagen degradation. This study was designed to evaluate the role of angiogenic vascular endothelial growth factor (VE
Publikováno v:
Journal of Cosmetic Dermatology. 21:3002-3006
BACKGROUND Pemphigus vulgaris (PV) is a debilitating autoimmune blistering disease of the skin and mucous membranes. It occurs due to the action of autoantibodies against various keratinocyte self-antigens. Anti-mitochondrial autoantibodies are detec
Autor:
Galal El‐Enany, Medhat El‐Mofty, Mona R.E. Abdel‐Halim, Dip Dermpath, Noha Nagui, Hanan Nada, Marwah Adly Saleh, Iman Sany, Ahmad Nada, Omar El‐Ghanam, Lobna Gamal Alieldin, Heba Ahmed Abdelkader
Publikováno v:
International Journal of Dermatology. 62
Autor:
Randa Mohammed Youssef, Marwah Adly Saleh, Mona Mostafa Korany, Zeinab A. Nour, Mona El‐Kalioby
Publikováno v:
Journal of cosmetic dermatologyREFERENCES.
E-cadherin is a classic cadherin that mediates keratinocyte adhesion.To assess the tissue expression of E-cadherin and its proteolytic serum fragment (soluble E-cadherin) in pemphigus vulgaris (PV) before and after clinical remission compared with co