Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Dourmishev, L."'
Autor:
Dourmishev L. A.
Publikováno v:
Acta Medica Bulgarica, Vol 51, Iss 3, Pp 63-69 (2024)
Autoimmune connective tissue diseases are a group of immune disorders, characterized by different clinical features, which affects not only the skin but also different organs and systems. Such diseases include: rheumatoid arthritis, systemic lupus er
Externí odkaz:
https://doaj.org/article/88d7f73edfbd4f02af9b3506fbbebbb9
Publikováno v:
Acta Medica Bulgarica, Vol 49, Iss 2, Pp 28-32 (2022)
Lupus erythematosus is an autoimmune connective tissue disorder showing a broad spectrum of clinical manifestations.
Externí odkaz:
https://doaj.org/article/6d9c3ec6263e4fc3bcd3607e3b9180fa
Autor:
Dourmishev L., Mironova N.
Publikováno v:
Acta Medica Bulgarica, Vol 48, Iss 3, Pp 68-76 (2021)
Atopic dermatitis (AD) is a chronic recurrent inflammatory skin disease in patients with atopy. Atopy itself, is defined as a predisposition to develop immune response with overproduction of immunoglobulin E to low doses of allergens. AD is one of th
Externí odkaz:
https://doaj.org/article/9ed81edb96f24ad3965de5052daed0bd
Publikováno v:
Acta Medica Bulgarica, Vol 48, Iss 3, Pp 46-48 (2021)
Erythema multiforme (EM) is an acute immune-mediated disease with multifactor etiology, which presents with symmetric target-like lesions on the skin. Probably the most common etiological factor of EM is viral infections, particularly herpes simplex
Externí odkaz:
https://doaj.org/article/5038efa843694b178f6f509ae27e7838
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.
Externí odkaz:
https://doaj.org/article/251079f65f894488830fc69ca07c1d2d
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
Externí odkaz:
https://doaj.org/article/ccd91bdf10a24851a3c1063bcabaf0c7
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
Externí odkaz:
https://doaj.org/article/d62a22ac85014fcb946326b85fc12baf
Publikováno v:
Acta Dermatovenerologica Croatica
Volume 28
Issue 3
Issue 2
Scopus-Elsevier
Volume 28
Issue 3
Issue 2
Scopus-Elsevier
Dear Editor, Paraneoplastic dermatomyositis is a distinct clinical variant of dermatomyositis (DM) in which the typical cutaneous features and muscle weakness appear before, simultaneously, or after the diagnosis of an internal malignancy. It occurs
Autor:
Rider, L. G., Ruperto, N., Pistorio, A., Erman, B., Bayat, N., Lachenbruc, P. A., Rockette, H., Feldman, B. M., Huber, A. M., Hansen, P., Oddis, C. V., Lundberg, I. E., Amato, A. A., Chinoy, H., Cooper, R. G., Chung, L., Danko, K., Fiorentino, D., De la Torre, I. G., Reed, A. M., Song, Y. W., Cimaz, R., Cuttica, R. J., Pilkington, C. A., Martini, A., van der Net, J., Maillard, S., Miller, F. W., Vencovsky, J., Aggarwal, R., Christopher-Stine, L., Criscione-Schreiber, L., Crofford, L., Cronin, M. E., Gordon, P., Hengstman, G., Katz, J. D., Mammen, A., Marder, G., Mchugh, N., Schiopu, E., Wolfe, G., Wortmann, R., Apaz, M., Bowyer, S., Constantin, T., Curran, M., Davidson, J., Griffin, T., Jones, O., Kim, S., Lang, B., Lindsley, C., Lovell, D., Magalhaes, C. S., Pachman, L. M., Ponyi, A., Punaro, M., Quartier, P., Ramanan, A. V., Ravelli, A., Rennebohm, R., Van Royen-Kerkhof, A., Sherry, D. D., Silva, C. A., Stringer, E., Wallace, C., Ascherman, D., Barohn, R., Benveniste, O., De Bleecker, J., Callen, J., Charles-Schoeman, C., Danoff, S., Dastmalchi, M., Dimachkie, M., Di Martino, S., Dourmishev, L., Ernste, F., Gono, T., Isenberg, D., Katsumata, Y., Kissel, J., Leff, R. L., Levine, T., Mann, H., Marie, I., Merola, J., Olesinska, M., Olsen, N., Pipitone, N., Ramchandren, S., Rutkove, S., Saketkoo, L. A., Schiffenbauer, A., Selva-O'Callaghan, A., Shinjo, S. K., Shupak, R., Swierkocka, K., de Visser, M., Wanschitz, J., Werth, V. P., Whitt, I., Ytterberg, S., Avcin, T., Becker, M., Beresford, M. W., Dressler, F., Dvergsten, J., Ferriani, V. P. L., Flato, B., Gerloni, V., Henrickson, M., Hinze, C., Hoeltzel, M., BUNES IBARRA, MIGUEL ANGEL, Ilowite, N., Imundo, L., Kingsbury, D., Magnusson, B., Maguiness, S., Mathiesen, P., Mccann, L., Nielsen, S., de Oliveira, S. K. F., Passo, M., Rabinovich, E., Rivas-Chacon, R., Robinson, A. B., Rouster-Stevens, K., Russo, R., Rutkowska-Sak, L., Sallum, A., Sanner, H., Schmeling, H., Selcen, D., Shaham, B., Spencer, C. H., Sundel, R., Tardieu, M., Thatayatikom, A., Wahezi, D., Zulian, F.
Publikováno v:
Rheumatology (Oxford, England), 56(11), 1884. Oxford University Press
Paediatric Rheumatology International Trials Organisation & International Myositis Assessment and Clinical Studies Group 2017, ' 2016 ACR-EULAR adult dermatomyositis and polymyositis and juvenile dermatomyositis response criteria-methodological aspects ', Rheumatology (Oxford, England), vol. 56, no. 11, pp. 1884-1893 . https://doi.org/10.1093/rheumatology/kex226
Paediatric Rheumatology International Trials Organisation & International Myositis Assessment and Clinical Studies Group 2017, ' 2016 ACR-EULAR adult dermatomyositis and polymyositis and juvenile dermatomyositis response criteria-methodological aspects ', Rheumatology (Oxford, England), vol. 56, no. 11, pp. 1884-1893 . https://doi.org/10.1093/rheumatology/kex226
Objective: The objective was to describe the methodology used to develop new response criteria for adult DM/PM and JDM.Methods: Patient profiles from prospective natural history data and clinical trials were rated by myositis specialists to develop c
Publikováno v:
Acta Medica Bulgarica; 2021, Vol. 47 Issue 4, p58-62, 5p