Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hana Buckova"'
Publikováno v:
Biomedical Papers, Vol 164, Iss 4, Pp 357-365 (2020)
Congenital ichthyoses are a very heterogeneous group of diseases manifested by dry, rough and scaling skin. In all forms of ichthyoses, the skin barrier is damaged to a certain degree. Congenital ichthyoses are caused by various gene mutations. Clini
Externí odkaz:
https://doaj.org/article/7fa64350f8b04136a7aa3025760df136
Autor:
Jemima E. Mellerio, Maya El Hachem, Nathalia Bellon, Giovanna Zambruno, Hana Buckova, Rudolf Autrata, Carmen Salavastru, Tamara Caldaro, Celine Greco, Cristina Has, Christine Bodemer
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Epidermolysis bullosa (EB) comprises a group of genetic disorders with the hallmark of fragility of the skin and mucosal surfaces. The severity of different types of EB varies markedly as does the occurrence of extra-cutaneous involvement an
Externí odkaz:
https://doaj.org/article/07f519bcf443446581d2b8e646e4026e
Autor:
Christine Bodemer, Cristina Has, Jemima E. Mellerio, N. Bellon, Céline Greco, Tamara Caldaro, Maya El Hachem, Hana Buckova, Rudolf Autrata, Giovanna Zambruno, Carmen Salavastru
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Epidermolysis bullosa (EB) comprises a group of genetic disorders with the hallmark of fragility of the skin and mucosal surfaces. The severity of different types of EB varies markedly as does the occurrence of extra-cutaneous involvement and complic
Publikováno v:
2021 19th International Conference on Emerging eLearning Technologies and Applications (ICETA).
Autor:
Carmen Salavastru, Jemima E. Mellerio, Cristina Has, Christine Bodemer, P Fischer, M. El Hachem, Céline Greco, Hana Buckova, P Nevoránková, Giovanna Zambruno, M Friedová
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADVReferences. 35(12)
Inherited epidermolysis bullosa (EB) comprises rare disorders that manifest with fragility and blistering of the skin and mucous membranes, with variable clinical severity. Management of EB is challenging due to disease rarity and complexity, the wid
Autor:
Jiri Dostal, Hana Buckova
Publikováno v:
2020 18th International Conference on Emerging eLearning Technologies and Applications (ICETA).
The article focuses on issues related to the innovation of the curriculum of informatics and digital technologies in the Czech Republic. Within the research survey, special attention is paid to the opinions of secondary school teachers. It is found o
Autor:
Hana Buckova, Jiri Dostal
Publikováno v:
2019 IEEE 15th International Scientific Conference on Informatics.
The process of implementing coding at schools attended by pupils from six to fourteen years of age is a current trend in developed countries. In some cases, simple activities involving coding might be even included at kindergartens attended by childr
Autor:
Jiri Dostal, Hana Buckova
Publikováno v:
2019 17th International Conference on Emerging eLearning Technologies and Applications (ICETA).
In the paper, we analyze the current state of education in the subject of Informatics at the level of primary schools in selected states of the European UnionFinland and Croatia. The trend of implementation of programming and algorithmization into te
Publikováno v:
Proceedings of the 2018 2nd International Conference on Education and E-Learning.
In this paper we discuss implementation of the curricular reform on the subject of Computing at the primary school level. The reason for this is the fact that there is a trend of implementation of programming and algorithmization in education in more
Autor:
Verena, Wally, Alain, Hovnanian, Juliette, Ly, Hana, Buckova, Victoria, Brunner, Thomas, Lettner, Michael, Ablinger, Thomas K, Felder, Peter, Hofbauer, Martin, Wolkersdorfer, Florian B, Lagler, Wolfgang, Hitzl, Martin, Laimer, Sophie, Kitzmüller, Anja, Diem, Johann W, Bauer
Publikováno v:
Journal of the American Academy of Dermatology. 78(5)
Epidermolysis bullosa simplex (EBS) is a rare genetic, blistering skin disease for which there is no cure. Treatments that address the pathophysiology of EBS are needed.Compare the impact of 1% diacerein cream with placebo in reducing the number of b