Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mirjana Paravina"'
Publikováno v:
Medicinski časopis
Brooke-Spiegler syndrome is a rare autosomal dominant hereditary disease with variable penetration. The syndrome is manifested by the appearance of three types of tumors: multiple cylindromas, trichoepitheliomas and spiradenomas. Tumors can cover the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::108ff0fdb5d6e878b752707a073e66b5
https://doi.org/10.5937/mckg51-14558
https://doi.org/10.5937/mckg51-14558
Autor:
Dragica Marković, Mirjana Paravina, Milenko Stanojević, Milanka Ljubenović, Milica Stepanović
Publikováno v:
Serbian Journal of Dermatology and Venereology, Vol 8, Iss 3, Pp 161-170 (2016)
Sarcoidosis is an acquired idiopathic granulomatous disease, which is characterized by noncaseating epithelioid granulomas in organs and tissues. Most frequently it affects the lungs, liver, lymph nodes, skin, eyes and other organs. The cutaneous les
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa476540ffa566467a6e8d9ce0c2ada
https://doi.org/10.1515/sjdv-2016-0014
https://doi.org/10.1515/sjdv-2016-0014
Autor:
Dragan Jovanović, Dragana Ljubisavljević, Danijela Popović, Mirjana Paravina, Vesna Karanikolic
Publikováno v:
Serbian Journal of Dermatology and Venereology, Vol 8, Iss 1, Pp 28-38 (2016)
Lichen myxedematosus, also known as papular mucinosis, is a primary diffuse cutaneous mucinosis. It is a rare cutaneous myxedematous condition characterized by formation of numerous lichenoid papules. Scleromyxedema, also known as Arndt–Gottron syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a7638dd60203aabe1ee76c950de27e5
https://doaj.org/article/3de3824fe96d43ed98b3ab6e13a65840
https://doaj.org/article/3de3824fe96d43ed98b3ab6e13a65840
Autor:
Mirjana Paravina
Publikováno v:
Journal of Dermatology & Cosmetology. 2
Introduction Skin is of crucial importance in the human system There are numerous factors that affect its appearance and function Various skin conditions and fast aging are manifestation of certain disturbances Aim To give information to dermatologis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::501cd2ab79737e32c99e95b71e486edf
https://doi.org/10.15406/jdc.2018.02.00101
https://doi.org/10.15406/jdc.2018.02.00101
Autor:
Jefta Kozarski, Gordana Savcic, Mirjana Milosavljević, Mirjana Paravina, Vladislav Krsti, Mirjana Milinkovic
Publikováno v:
Journal of Dermatology & Cosmetology. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8e368178d59d50f193b8468599f033b
https://doi.org/10.15406/jdc.2018.02.00029
https://doi.org/10.15406/jdc.2018.02.00029
Autor:
Ljiljana S. Spalević, Zorana Zlatanović, Milenko Stanojević, Mirjana Paravina, Dragana Ljubisavljević, Danijela Popović
Publikováno v:
Serbian Journal of Dermatology and Venereology, Vol 7, Iss 3, Pp 97-114 (2015)
Systemic scleroderma (SSc) is a multisystem disease with microvascular abnormalities, autoimmune disorders, excessive collagen production and deposition, and fibrosis of the skin and internal organs. According to the simplest, though incomplete class
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1b0e3ce766d34341142d00a96f64cd8
https://doaj.org/article/53ec15159b8544f9a4b82fbdde6962a1
https://doaj.org/article/53ec15159b8544f9a4b82fbdde6962a1
Publikováno v:
Serbian Journal of Dermatology and Venereology, Vol 7, Iss 2, Pp 61-68 (2015)
Yellow nail syndrome is a rare disease of unknown etiology. It is clinically characterized by a triad of yellow nails, lymphedema at one or more sites, and chronic respiratory disease (bronchitis, bronchiectasis and rhinosinusitis). All nails may be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::000d9f4d6252117360934aaecf154206
https://doi.org/10.1515/sjdv-2015-0006
https://doi.org/10.1515/sjdv-2015-0006
Autor:
Radmila Milenković, Mirjana Paravina, Danijela Popović, Dragana Ljubisavljević, Zorana Zlatanović
Publikováno v:
Serbian Journal of Dermatology and Venereology, Vol 7, Iss 1, Pp 15-22 (2015)
Verrucous epidermal nevi are noninflammatory, congenital, cutaneous hamartomas composed of keratinocytes, abnormal clone(s) of cells that reflect genetic mosaicism arising from different somatic mutations. Some of these mutations are well recognized,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaf9e8d6055d59cf615274b80f2a6849
https://doaj.org/article/61f031d1fb8949c08630d6e42366bb0b
https://doaj.org/article/61f031d1fb8949c08630d6e42366bb0b
Publikováno v:
Serbian Journal of Dermatology and Venereology, Vol 7, Iss 1, Pp 5-14 (2015)
Malignant acanthosis nigricans is a rare obligate paraneoplastic dermatosis which accounts for 20% of all acanthosis nigricans cases. The clinical features of the disease are the same as in the benign forms: symmetrical, hyperpigmented, velvety papil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c585c252e7520a2ad2b9671a3c620690
https://doaj.org/article/e337a02144b54b008ae33888d1265457
https://doaj.org/article/e337a02144b54b008ae33888d1265457
Publikováno v:
Serbian Journal of Dermatology and Venereology, Vol 6, Iss 4, Pp 174-185 (2014)
Pachydermodactyly is a rare, benign form of digital fibromatosis, characterized by asymptomatic and progressive, periarticular and usually symmetrical soft tissue finger swelling, specifically on the lateral aspects of the proximal interphalangeal jo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5df99c00dc65520fb4d611cc502fcb0
https://doaj.org/article/0673d3053ced4059b551a8f1b7b2c45a
https://doaj.org/article/0673d3053ced4059b551a8f1b7b2c45a