Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Enrique Garcia-Soler"'
Publikováno v:
Oman Journal of Ophthalmology, Vol 15, Iss 2, Pp 261-262 (2022)
Externí odkaz:
https://doaj.org/article/f30ac86d68ec4d619ba32807d76dc63c
Autor:
Enrique Garcia-Soler, Clara Martinez-Rubio, Marc D. De Smet, Patricia Udaondo, David Salom-Alonso
Publikováno v:
Acta Ophthalmologica. 100
Purpose to underline the importance of optical coherence tomography angiography (OCT-A) in the diagnosis, assessment of final visual outcome and better understanding of the Purtscher like retinopathy, as well as to emphasize on performing an ophthalm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2572500af59752055b7a53c14e532f7e
https://doi.org/10.1111/j.1755-3768.2022.0486
https://doi.org/10.1111/j.1755-3768.2022.0486
Publikováno v:
Oman journal of ophthalmology. 15(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec877c51aac8aeea86935f2951e9876a
https://pubmed.ncbi.nlm.nih.gov/35937737
https://pubmed.ncbi.nlm.nih.gov/35937737
Publikováno v:
Oman Journal of Ophthalmology, Vol 16, Iss 3, Pp 580-582 (2023)
Externí odkaz:
https://doaj.org/article/26aff2e6bc724134bdf4746ab49760d5
Autor:
Sara Fathi-Nieto, Rodrigo Butrón-Ruiz, Enrique García-Soler, Ana Hervás-Ontiveros, Amparo Ortiz-Seller
Publikováno v:
Oman Journal of Ophthalmology, Vol 15, Iss 3, Pp 385-388 (2022)
Spondyloocular syndrome (SOS) is a rare autosomal-recessive disorder. Since 2015, SOS has been linked to mutations in xylosyltransferase II (XYLT2) locus. Phenotypic features could affect multiple systems, such as sight, hearing, or bones. Herein, we
Externí odkaz:
https://doaj.org/article/e68a371ac8274e2abf947a5ec9d2c45d