Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Mariola Dorecka"'
Autor:
Xiaonan Liu, Anna Pacwa, Giorgia Bresciani, Marta Swierczynska, Mariola Dorecka, Adrian Smedowski
Publikováno v:
Molecular Medicine, Vol 30, Iss 1, Pp 1-14 (2024)
Abstract Primary cilia are sensory organelles that extend from the cellular membrane and are found in a wide range of cell types. Cilia possess a plethora of vital components that enable the detection and transmission of several signaling pathways, i
Externí odkaz:
https://doaj.org/article/bd0ceb0902444a55924bcb0841fec17c
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 14, p 4227 (2024)
Age-related macular degeneration (AMD) is the leading cause of irreversible blindness worldwide and a severe medical and social problem. The steadily increasing number of patients is related to the aging of the population. So far, many factors affect
Externí odkaz:
https://doaj.org/article/ddf0647d5e4641c6ad5d95fdaf6ea37a
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 10, p 5479 (2024)
Corneal neovascularization can impair vision and result in a poor quality of life. The pathogenesis involves a complex interplay of angiogenic factors, notably vascular endothelial growth factor (VEGF). This review provides a comprehensive overview o
Externí odkaz:
https://doaj.org/article/89fa16bc30e84520bc9647e7c0c20532
Autor:
Dorota Wyględowska-Promieńska, Marta Świerczyńska, Dorota Śpiewak, Dorota Pojda-Wilczek, Agnieszka Tronina, Mariola Dorecka, Adrian Smędowski
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 5, p 2928 (2024)
Aland island eye disease (AIED), an incomplete form of X-linked congenital stationary night blindness (CSNB2A), and X-linked cone-rod dystrophy type 3 (CORDX3) display many overlapping clinical findings. They result from mutations in the CACNA1F gene
Externí odkaz:
https://doaj.org/article/d144746302754f8ca19febf44f677ccd
Publikováno v:
Life, Vol 14, Iss 1, p 14 (2023)
Purpose: To examine the effectiveness of a standardized combination of intracameral mydriatics and anesthetic (SCIMA) on mydriasis in patients with coexisting diseases such as diabetes mellitus (DM) and pseudoexfoliation syndrome (PXF) during phacoem
Externí odkaz:
https://doaj.org/article/3c6f328236f643f89d1d274bd29e00ce
Autor:
Małgorzata Sobolewska, Marta Świerczyńska, Mariola Dorecka, Dorota Wyględowska-Promieńska, Maciej R. Krawczyński, Ewa Mrukwa-Kominek
Publikováno v:
Medicina, Vol 59, Iss 2, p 399 (2023)
Background: Cone–rod dystrophies (CRDs) are a heterogeneous group of inherited retinal diseases (IRDs) characterized by cone photoreceptor loss, that is followed by subsequent rod photoreceptor impairment. Case presentation: A 49-year-old man compl
Externí odkaz:
https://doaj.org/article/1b2f7f5a182f48b0aa5711294753182b
Publikováno v:
Klinika Oczna. 125:50-55
Publikováno v:
Klinika Oczna. 124:1-6
Publikováno v:
Ophthalmology Journal. 5:114-119
The ocular ischemic syndrome (OIS) is a rare condition with vision-threatening potentials. It is characterized by chronic ischemia of the anterior and/or posterior segment of the eye primarily caused by severe carotid artery occlusive diseases. In th
Autor:
Jaromir Wasyluk, Joanna Dereń, Dorota Wyględowska-Promieńska, Agata Niedzielska-Krycia, Mariola Dorecka
Publikováno v:
OphthaTherapy. Therapies in Ophthalmology. 6:233-242
Endophthalmitis is a rare, but very severe form of ocular inflamation. Inflammatory process involves all types of intraocular liquids and tissues. It is usually accompanied by lowered of visual acuity, pain and notable inflammation of anterior segmen