In the face of an “epidemic” increase in myopia over the last decades and myopia prevalence predicted to reach 2.5 billion people by the end of this decade, there is an urgent need to develop effective and safe therapeutic interventions to…
To identify genetic mutations in three families with early onset high myopia (eoHM) limited to female members. Genomic DNA was collected from participating members of families XF1, XF2, and XF3.
81895758839763https://smlouvy.gov.cz/smlouva/88397632019-04-24T08:40:47 02:00b4hbqavMěsto Přelouč00274101Město Přelouč, Československé armády 1665, 53533 PřeloučNeurčenoLukáš Slabý69169667SemínDodatek č.
Identification of the association of specific signs of dry eye disease with specific visual function deficits may allow for more targeted approaches to treatment. To explore the association of dry eye signs and symptoms with visual acuity…