Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Ivelina Yordanova"'
Autor:
Preslav Vasilev, Savelina Popovska, Elitsa Petrova Kraevska, Martin Karamanliev, Dobromir Dimitrov, Ivelina Yordanova
Publikováno v:
Dermatology Practical & Conceptual, Vol 14, Iss 3 (2024)
Introduction: Squamous cell carcinoma of the skin (SCCs) is the second most common skin cancer with continuously increasing incidence. Programmed cell death ligand 1 (PD-L1), Programmed cell death 1 receptor (PD-1) and CD8 expression in primary SCCs
Externí odkaz:
https://doaj.org/article/403beb98d68347a399733afeb05d186b
Publikováno v:
Case Reports in Dermatology, Vol 16, Iss 1, Pp 47-54 (2024)
Introduction: Netherton syndrome (NS) is a rare autosomal recessive genodermatosis in the group of congenital ichthyosis. The clinical manifestations of the syndrome vary from a very mild clinical manifestation occurring with the picture of ichthyosi
Externí odkaz:
https://doaj.org/article/764115ca868d4d28b32263aaf8002cd5
Autor:
Polina Kostova, Guergana Petrova, Martin Shahid, Vera Papochieva, Dimitrinka Miteva, Ivelina Yordanova, Kossara Drenovska, Irena Bradinova, Camila K. Janniger, Robert A. Schwartz, Snejina Vassileva
Publikováno v:
Clinical Case Reports, Vol 12, Iss 4, Pp n/a-n/a (2024)
Key Clinical Message High‐dose intravenous immunoglobulin exhibits great potential in the treatment of Netherton syndrome. Abstract Netherton syndrome (NS) is a rare autosomal recessive genodermatosis (OMIM #256500) characterized by superficial sca
Externí odkaz:
https://doaj.org/article/43f0b4cfd07c4faca5422ca51dfd9ab6
Publikováno v:
Journal of IMAB, Vol 29, Iss 4, Pp 5139-5144 (2023)
Introduction: The incidence of Squamous cell carcinoma of the skin (SCCs) increases annually, and this process will likely be continued because of sun exposure, outdoor activities and the aging population. Objectives: The aim of our study is to analy
Externí odkaz:
https://doaj.org/article/9410c8f6a92046c9859863f9736d6fc6
Publikováno v:
Journal of IMAB, Vol 26, Iss 3, Pp 3245-3250 (2020)
Purpose: Epidermolysis bullosa pruriginosa (EBP) is a rare clinical subtype of inherited Epidermolysis bullosa dystrophica (EBD). It is characterized by severe itching and hypertrophic papules affecting the extensor surfaces of the extremities. Mate
Externí odkaz:
https://doaj.org/article/989a1d9d1384446598239c89576b171f
Publikováno v:
Journal of IMAB, Vol 26, Iss 2, Pp 3174-3176 (2020)
Contact dermatitis is an acute or chronic inflammatory reaction in response to substances coming into contact with the skin. Differentiating between irritant contact dermatitis and allergic contact dermatitis in practice, as well as finding the exact
Externí odkaz:
https://doaj.org/article/b36f80a09f174a1089175a49fce70c70
Autor:
Sara Guerrero-Aspizua, Claudio J. Conti, Maria Jose Escamez, Daniele Castiglia, Giovanna Zambruno, Leila Youssefian, Hassan Vahidnezhad, Luis Requena, Peter Itin, Gianluca Tadini, Ivelina Yordanova, Ludovic Martin, Jouni Uitto, Cristina Has, Marcela Del Rio
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-15 (2019)
Abstract Background Kindler Syndrome (KS) is a rare genodermatosis characterized by skin fragility, skin atrophy, premature aging and poikiloderma. It is caused by mutations in the FERMT1 gene, which encodes kindlin-1, a protein involved in integrin
Externí odkaz:
https://doaj.org/article/2039cab014194ad7a6c6aa5ac424b587
Autor:
Desislava Tsvetanova, Ivelina Yordanova, Hristina Haidudova, Klimentina Gospodinova, Verka Pavlova, Maya Alexieva, Milen Karaivanov, Dimitar Gospodinov
Publikováno v:
Journal of IMAB, Vol 25, Iss 1, Pp 2443-2446 (2019)
Combination between Leucocytoclastic vasculitis and Subacute cutaneous lupus erythematosus has been only rarely reported in the literature. Pathological cutaneous lesions are presented by purpura, erythematous macules, urticarial, nodules and necrose
Externí odkaz:
https://doaj.org/article/935b7dc5b4e64ec8924dde8d05b2e918
Autor:
Ivelina Yordanova, Valentin Valtchev, Kossara Drenovska, Dimitar K. Gospodinov, Snejina Vassileva
Publikováno v:
Journal of IMAB, Vol 20, Iss 6, Pp 552-555 (2014)
Herpes gestationis, also known as pemphigoidgestationis (PG) is an extremely rare autoimmune bullous dermatosis of the gestation and postpartum period. The disease was originally named herpes gestationis on the basis of the morphological herpetiform
Externí odkaz:
https://doaj.org/article/ee324d0d6e9f4e2a9b82293a21057afc
Publikováno v:
Journal of IMAB, Vol 21, Iss 4, Pp 1012-1014 (2015)
IgA linear bullous dermatosis, also known as chronic bullous dermatosis of childhood, is an autoimmune disease which may be idiopathic or drug-induced. The disease affects children and adults. We present a 4 years old girl with itchy polymorphic erup
Externí odkaz:
https://doaj.org/article/bedb4020513549e288ee830f44d87924