Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Sawsan R, Nowilaty"'
Publikováno v:
Journal of Ophthalmic Inflammation and Infection, Vol 12, Iss 1, Pp 1-5 (2022)
Externí odkaz:
https://doaj.org/article/cb3926d154894926bd3dda24637954d1
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 26, Iss , Pp 101514- (2022)
Purpose: To report novel life-threatening coronary and systemic arterial disease associated with Retinal Arterial Macroaneurysms with Supravalvular Pulmonic Stenosis (RAMSVPS) syndrome, previously known as Familial Retinal Arterial Macroaneurysms (FR
Externí odkaz:
https://doaj.org/article/163f318890b44eea97e3ffb82bf4965e
Autor:
Moustafa S. Magliyah, Faisal Almarek, Sawsan R. Nowilaty, Lama Al-Abdi, Fowzan S. Alkuraya, Mohammed Alowain, Patrik Schatz, Talal Alfaadhel, Arif O. Khan, Sulaiman M. Alsulaiman
Publikováno v:
Retina. 43:498-505
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1da3b43c94d6d4176a93beae6de089e
https://doi.org/10.1097/iae.0000000000003691
https://doi.org/10.1097/iae.0000000000003691
Autor:
Hamad F Alsubaie, Abdulrahman AlZaid, Moustafa S. Magliyah, Sawsan R. Nowilaty, Osama AlRaddadi
Publikováno v:
RETINAL Cases & Brief Reports. 17:206-211
Purpose To report a case of Stickler type IV with familial exudative vitreoretinopathy (FEVR) phenotype. Material and methods Retrospective case report. Results A 24-year-old female presented with right eye exotropia and decreased vision. She had no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::842857fd19dee9f3fe298fff51f587ef
https://doi.org/10.1097/icb.0000000000001155
https://doi.org/10.1097/icb.0000000000001155
Publikováno v:
Ophthalmology Retina. 5:918-927
Purpose To highlight recognizable patterns of subretinal fibrosis in enhanced S-cone syndrome (ESCS). Design Retrospective case series. Participants Forty-seven patients with subretinal fibrosis identified from 101 patients with clinically diagnosed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fec22f3f576f7fd9a505d5cc4fff3dae
https://doi.org/10.1016/j.oret.2021.03.014
https://doi.org/10.1016/j.oret.2021.03.014
Publikováno v:
Ophthalmic Genetics. 42:204-208
Background: Gyrate atrophy of the choroid and retina (GA) is a rare autosomal recessive disorder characterized by nyctalopia, myopia, sharply demarcated expanding peripheral chorioretinal atrophic ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f6f3080093e683eb0a98385fa2aef9c
https://doi.org/10.1080/13816810.2020.1843185
https://doi.org/10.1080/13816810.2020.1843185
Publikováno v:
Documenta Ophthalmologica. 142:239-245
To describe the stages of development and natural course of a full-thickness macular hole (FTMH) in a patient with enhanced S-cone syndrome (ESCS). This study reported the serial ophthalmologic examinations and macular spectral-domain optical coheren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f138c332e3dfee1c9a7d48c6b2f5e9cc
https://doi.org/10.1007/s10633-020-09787-8
https://doi.org/10.1007/s10633-020-09787-8
Publikováno v:
RETINAL Cases & Brief Reports. 14:203-210
PURPOSE: To describe a specific cone-rod dystrophy phenotype in a family with the homozygous c.1429G>A; p.Gly477Arg mutation in CRB1. The detailed phenotype of subjects with this specific mutation has not been described previously. METHODS: Clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d462bd638c98b2a49acd3a72a98e8bb
https://doi.org/10.1097/icb.0000000000000654
https://doi.org/10.1097/icb.0000000000000654
Publikováno v:
Journal of ophthalmic inflammation and infection. 12(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c188f02cc654b11439605dc85b451c4
https://pubmed.ncbi.nlm.nih.gov/35522341
https://pubmed.ncbi.nlm.nih.gov/35522341
Autor:
Abdullah S. Al-Kharashi, Ahmed M. Abu El-Asrar, Emad B. Abboud, Bandar Alamro, Fowzan S. Alkuraya, Ramadan Alturki, Rana Helaby, Niema Ibrahim, Bandar Al Ghamdi, Hisham Alkuraya, Nisha Patel, Mohammed D. Alotaibi, Sawsan R. Nowilaty, Abdulrahman Al-Hussaini, Sulaiman M. Alsulaiman, Amani Elshaer, Zainab Almasseri, Hamad Al-Zaidan, Naif A.M. Almontashiri, Wafaa Eyaid
Publikováno v:
Clinical Genetics. 97:447-456
Retinal arterial macroaneurysms with supravalvular pulmonic stenosis (RAMSVPS), also known as Familial Retinal Arterial Macroaneurysms (FRAM) syndrome, is a very rare multisystem disorder. Here, we present a case series comprising ophthalmologic and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::131e77cfe46d6a6dea26638ff5239fcd
https://doi.org/10.1111/cge.13676
https://doi.org/10.1111/cge.13676