Zobrazeno 1 - 10
of 38
pro vyhledávání: '"S. Shaya"'
Autor:
R. D. Sawaya, T. El Zahran, S. Mrad, C. Abdul Massih, S. Shaya, M. Makki, H. Tamim, M. Majdalani
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background It is not yet known how antibiotics may affect Serious Bacterial Infections (SBI). Our aim is to describe the presentation, management, and serious bacterial infections (SBI) of febrile children on or off antibiotics. Methods Retr
Externí odkaz:
https://doaj.org/article/50daa07856374b3db9cf6352bb40ee10
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 27, Iss , Pp 101633- (2022)
Externí odkaz:
https://doaj.org/article/b02dfccddf524afca94a8461c3d5ef4f
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::058c25586d974ff9a27b6e4cb13931f9
https://doi.org/10.1177/24741264221120490
https://doi.org/10.1177/24741264221120490
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e207d2167adc41e54d4461c1bdcd31d
https://doi.org/10.1097/iae.0000000000003611
https://doi.org/10.1097/iae.0000000000003611
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bacc7bee9496d77ecb89d159050417d5
https://doi.org/10.1016/j.oret.2022.02.003
https://doi.org/10.1016/j.oret.2022.02.003
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e3abebd25a447f12054174b72230c7b
https://doi.org/10.1080/13816810.2021.2010771
https://doi.org/10.1080/13816810.2021.2010771
Akademický článek
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Autor:
L. Sadozai, S. Shaya, P. Coste, E. Le Roux, C. Guillot, P. Boizeau, O. Bourdon, S. Prot-Labarthe
Publikováno v:
Le Pharmacien Clinicien. 57:e28-e29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3555d0b35b05b65911bdb4a9eea9d83b
https://doi.org/10.1016/j.phacli.2022.10.413
https://doi.org/10.1016/j.phacli.2022.10.413
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