Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ensieh Darbari"'
Autor:
Ensieh Darbari, Hamid Ahmadieh, Narsis Daftarian, Mozhgan Rezaei Kanavi, Fatemeh Suri, Hamideh Sabbaghi, Elahe Elahi
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 17, Iss 1, Pp 51-58 (2022)
Abstract Purpose: Stargardt disease type 1 (STGD1) is a recessively inherited retinal disorder that can cause severe visual impairment. ABCA4 mutations are the usual cause of STGD1. ABCA4 codes a transporter protein exclusively expressed in retinal p
Externí odkaz:
https://doaj.org/article/49a6e618ea1d451496fa3fd3130670a1
Autor:
Ensieh, Darbari, Hamid, Ahmadieh, Narsis, Daftarian, Mozhgan, Rezaei Kanavi, Fatemeh, Suri, Hamideh, Sabbaghi, Elahe, Elahi
Publikováno v:
Journal of ophthalmicvision research. 17(1)
Stargardt disease type 1 (STGD1) is a recessively inherited retinal disorder that can cause severe visual impairment.Eighteen STGD1 patients were recruited for genetic analysis. Diagnosis by retina specialists was based on standard criteria, includin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::456582bf6732cb6c7811f378c358bdb7
https://pubmed.ncbi.nlm.nih.gov/35194496
https://pubmed.ncbi.nlm.nih.gov/35194496
Autor:
Ensieh, Darbari, Davood, Zare-Abdollahi, Afagh, Alavi, Mozhgan, Rezaei Kanavi, Sepehr, Feizi, Seyed Bagher, Hosseini, Alireza, Baradaran-Rafii, Hamid, Ahmadieh, Shohreh, Issazadeh-Navikas, Elahe, Elahi
Publikováno v:
Molecular vision. 26
Peters anomaly (PA) is a heterogeneous developmental disorder characterized by central corneal opacity and iridocorneal or corneolenticular adhesions. Although many causative genes have been identified, most screened patients do not have mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d53ecf1b62c28d1eede7bf2ce463a22b
https://pubmed.ncbi.nlm.nih.gov/33273802
https://pubmed.ncbi.nlm.nih.gov/33273802