Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Marianna Kousparou"'
Autor:
Maria G. Koliou, Athina Aristidou, Stella Mazeri, Elena Georgiou, Maria Agathocleous, Marianna Kousparou, Avraam Elia, Antonis Jossif
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Kawasaki disease (KD) is one of the most common vasculitides of early childhood. There are no previous studies on KD in Cyprus. The aim of this study was to evaluate the epidemiology of KD in Cyprus, risk factors for resistance to treatment
Externí odkaz:
https://doaj.org/article/3f13983b30544f70b786d81b94c6f8bb
Autor:
Maria G Koliou, Athina Aristidou, Stella Mazeri, Elena Georgiou, Maria Agathocleous, Marianna Kousparou, Avraam Elia, Antonis Jossif
Publikováno v:
Koliou, M G, Aristidou, A, Mazeri, S, Georgiou, E, Agathocleous, M, Kousparou, M, Elia, A & Jossif, A 2023, ' Epidemiology and risk factors for resistance to treatment of Kawasaki disease in Cyprus ', Scientific Reports, vol. 13, no. 1, 352, pp. 1-8 . https://doi.org/10.1038/s41598-023-27694-1
Background: Kawasaki disease (KD) is one of the most common vasculitides of early childhood and the first cause of acquired heart disease in developed countries. There are no previous studies on KD in Cyprus. The aim of this study was to evaluate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b01a8d52c487de1cc5f3cb4009cfe235
https://doi.org/10.21203/rs.3.rs-1150812/v1
https://doi.org/10.21203/rs.3.rs-1150812/v1
Autor:
Marianna Kousparou, Adamos Hadjipanayis, Nicos Skordis, Violetta Christophidou-Anastasiadou, Christos Shammas, Alkis Pierides, Sophia Kyriakou, Christina Kyriakou, Constantina Costi, Michalis Iasonides, Vick N Atamyan, Leonidas A. Phylactou, Tassos C. Kyriakides, Margarita Onoufriou, George A. Tanteles, Vassos Neocleous, Meropi Toumba, Maria Koliou
Publikováno v:
Annals of Human Genetics. 79:20-27
Familial Mediterranean fever (FMF) is caused by mutations in the MEFV gene and the spectrum of mutations among Greek-Cypriots with FMF-related symptoms was examined. Sequence analysis for exons 2, 3, 5, and 10 of the MEFV gene was performed in a coho