Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Lyubomir, Dourmishev"'
Publikováno v:
Folia Medica, Vol 64, Iss 4, Pp 682-687 (2022)
Aortoiliac occlusive disease (AIOD) is non-inflammatory obstructive vasculopathy commonly affecting patients with advanced atherosclerosis, diabetes mellitus, or elevated cholesterol levels, and subjects with other risk factors such as cigarette smok
Externí odkaz:
https://doaj.org/article/436a06acd58e4040b63a08b63ae543a8
Publikováno v:
Dermatology Practical & Conceptual, Vol 12, Iss 3 (2022)
Introduction: Dermoscopy is a noninvasive and easy to apply technique that allows in vivo magnification of the skin and thus observation of morphologic structures invisible to the naked eye. Recently, it gained popularity for evaluation of inflammato
Externí odkaz:
https://doaj.org/article/cf1a6453b2e946b4b5de74347e3881ab
Publikováno v:
Indian Journal of Dermatology, Venereology and Leprology. 88:658-660
Publikováno v:
Dermatologic Therapy. 35
Autor:
Dimitrina Guleva, Lyubomir Dourmishev
Publikováno v:
Clinics in Dermatology
Ultraviolet (UV) therapy is an effective and well tolerated therapeutic method for various dermatologic conditions due to its antiproliferative and immunosuppressive effects. Contemporary phototherapy (PhT) includes broadband UVB, narrowband UVB, UVA
Autor:
Lyubomir Dourmishev, Radoslava Saraeva, Radka Kaneva, Darina Kachakova, Joana Pozharashka, Zornitsa Kamenarska, Neviana Ivanova, Anton Vinkov, Gyulnas Dzhebir, Maria Hristova
Publikováno v:
Immunological Investigations. 51:817-825
Background: Decreased expression of the T cell receptor (TCR) ζ-chain has been reported in autoimmune diseases. Recent evidence suggests that this deficiency may be due to polymorphisms in the CD3Z...
Publikováno v:
Acta Medica Bulgarica, Vol 47, Iss 4, Pp 58-62 (2020)
Graham-Little-Piccardi-Lassueur syndrome (GLPLS) is a rare syndrome characterized by the triad of cicatricial alopecia of the scalp, non-cicatricial alopecia of the axilla and groin and follicular lichen planus eruptions on the trunk and extremities.
Publikováno v:
Acta Medica Bulgarica, Vol 47, Iss 2, Pp 43-46 (2020)
Neurofibromatosis type I is an autosomal dominant genetic disorder with an incidence of about 1 in 3000 births. Apart from the typical skin involvement NF1 may affect multiple organs with ocular, neurological, skeletal and cardiovascular manifestatio
Publikováno v:
Acta Medica Bulgarica, Vol 47, Iss 2, Pp 30-33 (2020)
The group of congenital limb overgrowth syndromes associated with vascular malformations include various disorders, often with variable clinical expression. Klippel-Trenaunay syndrome is the most common syndrome in this group, compared to other simil
Autor:
Joana Pozharashka, Maria Hristova, Zornitsa Kamenarska, Radka Kaneva, Kalina Mihova, Gyulnas Dzhebir, Rozalia Hristova, Anton Vinkov, Svetla Nikolova, Tsvetoslav Georgiev, Alexey Savov, Lyubomir Dourmishev, Atanas Koundurdjiev
Publikováno v:
Rheumatology international. 41(12)
Systemic lupus erythematosus (SLE) is a multifactorial autoimmune disease and polymorphisms in the cytokine genes and their receptors are thought to influence its development. The aim of this case–control study was to investigate the association of