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Sökning: WFRF:(Stankiewicz R.) > (2020-2022)

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1.
  • Kunze, M, et al. (författare)
  • Recommendations to Improve Tick-Borne Encephalitis Surveillance and Vaccine Uptake in Europe
  • 2022
  • Ingår i: Microorganisms. - : MDPI AG. - 2076-2607. ; 10:7
  • Tidskriftsartikel (refereegranskat)abstract
    • There has been an increase in reported TBE cases in Europe since 2015, reaching a peak in some countries in 2020, highlighting the need for better management of TBE risk in Europe. TBE surveillance is currently limited, in part, due to varying diagnostic guidelines, access to testing, and awareness of TBE. Consequently, TBE prevalence is underestimated and vaccination recommendations inadequate. TBE vaccine uptake is unsatisfactory in many TBE-endemic European countries. This review summarizes the findings of a scientific workshop of experts to improve TBE surveillance and vaccine uptake in Europe. Strategies to improve TBE surveillance and vaccine uptake should focus on: aligning diagnostic criteria and testing across Europe; expanding current vaccine recommendations and reducing their complexity; and increasing public education of the potential risks posed by TBEV infection.
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2.
  • Swierkowska, Joanna, et al. (författare)
  • Variants in FLRT3 and SLC35E2B identified using exome sequencing in seven high myopia families from Central Europe
  • 2021
  • Ingår i: Advances in Medical Sciences. - : ELSEVIER URBAN & PARTNER SP Z O O. - 1896-1126 .- 1898-4002. ; 66:1, s. 192-198
  • Tidskriftsartikel (refereegranskat)abstract
    • Purpose: High myopia (HM) is an eye disorder with both environmental and genetic factors involved. Many genetic factors responsible for HM were recognized worldwide, but little is known about genetic variants underlying HM in Central Europe. Thus, the aim of this study was to identify rare sequence variants involved in HM in families from Central Europe to better understand the genetic basis of HM. Materials and methods: We assessed 17 individuals from 7 unrelated Central European families with hereditary HM using exome sequencing (ES). Segregation of selected variants in other available family members was performed using Sanger sequencing. Results: Detected 73 rare variants were selected for verification. We observed 2 missense variants, c.938C>T in SLC35E2B - encoding solute carrier family 35 member E2B, and c.1642G>C in FLRT3 - encoding fibronectin leucine rich transmembrane protein, segregating with HM in one family. Conclusions: FLRT3 and/or SLC35E2B could represent disease candidate genes and identified sequence variants might be responsible for HM in the studied family.
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