Zobrazeno 1 - 10
of 259
pro vyhledávání: '"L Miteva"'
Publikováno v:
Bulgarian Journal of Veterinary Medicine, Vol 27, Iss 3, Pp 375-386 (2024)
The aim of the study was to develop a molecular diagnosis protocol of monocytic ehrlichiosis and granulocytic anaplasmosis in dogs by conventional polymerase chain reaction (PCR) and to compare the results from PCR and a rapid serological test. One h
Externí odkaz:
https://doaj.org/article/a7a53e753738466e8fed578cc721adf6
Autor:
K. Yovchev, L. Miteva
Publikováno v:
Mechanical Sciences, Vol 13, Pp 427-436 (2022)
The main purpose of the iterative learning control (ILC) method is to reduce the trajectory tracking error caused by an inaccurate model of the robot's dynamics. It estimates the tracking error and applies a learning operator to the output control si
Externí odkaz:
https://doaj.org/article/baaa1792a411455ab49a81faeb0949c0
Publikováno v:
Acta Medica Bulgarica. 49:28-32
Lupus erythematosus is an autoimmune connective tissue disorder showing a broad spectrum of clinical manifestations. The aim of this study was to assess the correlation of skin histology and different types of lupus erythematosus. Materials and metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7af05b00812bc8dcede9cad6b25cd1d6
https://doi.org/10.2478/amb-2022-0016
https://doi.org/10.2478/amb-2022-0016
Akademický článek
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Publikováno v:
Journal of Investigative Dermatology. 143:S29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3560d26019ae97132b5cae23aad2d73
https://doi.org/10.1016/j.jid.2023.03.172
https://doi.org/10.1016/j.jid.2023.03.172
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::28d9c4f4ad60985a36552ecc63ca1dbd
https://doi.org/10.2478/amb-2020-0020
https://doi.org/10.2478/amb-2020-0020
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::954979ce9bf0c59d836250614c813aae
https://doi.org/10.2478/amb-2020-0023
https://doi.org/10.2478/amb-2020-0023
Publikováno v:
Journal of Investigative Dermatology. 142:S267
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdd4f0e9abd757f58cc8fa5b9c9d2d99
https://doi.org/10.1016/j.jid.2022.09.516
https://doi.org/10.1016/j.jid.2022.09.516
Autor:
Snejina Vassileva, Lyubomir Dourmishev, Dimitrina Guleva, L. Miteva, Kossara Drenovska, Joana Pozharashka
Publikováno v:
Clinics in Dermatology
Autoimmune connective tissue diseases are a heterogeneous group of clinical entities sharing a common feature-an impairment of structural components like collagen and elastin, arising by autoimmune mechanisms. Because most patients are on a long-term
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80f73d5ea612f0084676d142b47bec15
https://pubmed.ncbi.nlm.nih.gov/33972054
https://pubmed.ncbi.nlm.nih.gov/33972054
