Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Fadi S. Shaya"'
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 27, Iss , Pp 101633- (2022)
Externí odkaz:
https://doaj.org/article/b02dfccddf524afca94a8461c3d5ef4f
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 15, Iss , Pp - (2019)
Purpose: To highlight the striking similarities between the lesions of congenital toxoplasmosis (CT) and North Carolina Macular Dystrophy (NCMD) using multimodal imaging including spectral domain optical coherence tomography (SD-OCT). Observations: W
Externí odkaz:
https://doaj.org/article/38cdb92a8584490eb293adcf8cf7636c
Publikováno v:
Journal of VitreoRetinal Diseases. 7:109-115
Purpose: To report the results of a nonsurgical approach to repair macular holes (MHs). Methods: A retrospective chart review of consecutive patients with MHs from 2018 to 2021 was performed. Topical therapy consisted of a steroidal agent, a nonstero
Autor:
Kent W. Small, Caroline A. Tawfik, Nitin Udar, Uma Udar, Jessica Avetisjan, Lamia A. El-aidy, Fadi S. Shaya
Publikováno v:
Retina. 42:2379-2387
Autor:
Kent W. Small, Robert Wiggins, Nitin Udar, Rosemary Silva-Garcia, Jessica Avetisjan, Andrea Vincent, Fadi S. Shaya
Publikováno v:
Ophthalmology Retina. 6:512-519
The phenotype of North Carolina macular dystrophy (NCMD) is highly variable and remains poorly appreciated and understood, often causing misdiagnoses in isolated cases. One of the features of NCMD is the general lack of progression despite its origin
Autor:
Kent W. Small, Stijn Van de Sompele, Jessica Avetisjan, Nitin Udar, Steven Agemy, Elfride De Baere, Fadi S. Shaya
Publikováno v:
JOURNAL OF VITREORETINAL DISEASES
Purpose:To clinically and molecularly study a newly found family with North Carolina macular dystrophy (NCMD/MCDR1) from Mexico.Methods:This retrospective study comprised 6 members of a 3-generation Mexican family with NCMD. Clinical ophthalmic exami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d800469665fa9512561f13909d4510da
https://hdl.handle.net/1854/LU-01GTHEVYCZYEWACGEMQGN894GE
https://hdl.handle.net/1854/LU-01GTHEVYCZYEWACGEMQGN894GE
Autor:
Kent W. Small, Lee M. Jampol, Benjamin Bakall, Leslie Small, Robert Wiggins, Steven Agemy, Nitin Udar, Jessica Avetisjan, Andrea Vincent, Fadi S. Shaya
Publikováno v:
Ophthalmic Genetics. 43:307-317
North Carolina Macular Dystrophy (NCMD) and Best Vitelliform Macular Dystrophy (BVMD) are rare autosomal dominant macular dystrophies. Both BVMD and NCMD have markedly variable expressivity. In some individuals, it can be difficult to differentiate b
Autor:
Stijn Van de Sompele, Kent W. Small, Munevver Burcu Cicekdal, Víctor López Soriano, Eva D’haene, Fadi S. Shaya, Steven Agemy, Thijs Van der Snickt, Alfredo Dueñas Rey, Toon Rosseel, Mattias Van Heetvelde, Sarah Vergult, Irina Balikova, Arthur A. Bergen, Camiel J. F. Boon, Julie De Zaeytijd, Chris F. Inglehearn, Bohdan Kousal, Bart P. Leroy, Carlo Rivolta, Veronika Vaclavik, Jenneke van den Ende, Mary J. van Schooneveld, José Luis Gómez-Skarmeta, Juan J. Tena, Juan R. Martinez-Morales, Petra Liskova, Kris Vleminckx, Elfride De Baere
North Carolina macular dystrophy (NCMD) is a rare autosomal dominant disease affecting macular development. The disease is caused by non-coding single nucleotide variants (SNVs) in two hotspot regions near PRDM13 and by duplications in two distinct c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79feee9e3f4666cf8b923858f2090fe3
https://doi.org/10.1101/2022.03.08.481329
https://doi.org/10.1101/2022.03.08.481329
Autor:
Kent W, Small, Stijn, Van de Sompele, Karen, Nuytemans, Andrea, Vincent, Ozge Ozalp, Yuregir, Emine, Ciloglu, Cahfer, Sariyildiz, Toon, Rosseel, Jessica, Avetisjan, Nitin, Udar, Jeffery M, Vance, Margaret A, Pericak-Vance, Elfride, De Baere, Fadi S, Shaya
Publikováno v:
Molecular Vision
Purpose To clinically and molecularly investigate a new family with North Carolina macular dystrophy (NCMD) from Turkey, a previously unreported geographic origin for this phenotype. Methods Clinical ophthalmic examinations, including fundus imaging
Autor:
Jennifer I. Lim, Adam R. Glassman, Lloyd Paul Aiello, Usha Chakravarthy, Christina J. Flaxel, Lawrence J. Singerman, Richard F. Spaide, Daniel B. Roth, Lloyd P. Aiello, Jorge G. Arroyo, Sophie J. Bakri, Charlie C. Barr, Caroline R. Baumal, Kevin J. Blinder, Nauman Chaudhry, Victor Chong, Albert O. Edwards, Allan Hunter, Michael J. Elman, Michel E. Farah, Gary Fish, Alfonso Giovannini, Frank G. Holz, Rahul N. Khurana, Gregg T. Kokame, H. Richard McDonald, Stephan Michels, Roger L. Gary Novack, Maurizio Battaglia Parodi, Carl D. Regillo, Kent W. Small, Fadi S. Shaya, Rickard F. Spaide, Giovani Staurenghi, Jennifer Sun, Demetrios Vavvas, Charles Wykoff, Lucy H.Y. Young
Publikováno v:
Ophthalmology. Retina. 1(5)
Purpose To assess anatomic and visual outcomes of ocriplasmin use for symptomatic vitreomacular adhesion (VMA). Design Retrospective chart review. Methods Macula Society members were surveyed online to collect data on ocriplasmin for symptomatic VMA.