Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ashley López-Cañizares"'
Autor:
Ashley López-Cañizares, Hasenin Al-khersan, Maria P. Fernandez, Benjamin R. Lin, Lediana Goduni, Audina M. Berrocal
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 27:100-102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e125c6c6fa061f5b3e843338bfb7c0eb
https://doi.org/10.1016/j.jaapos.2022.11.007
https://doi.org/10.1016/j.jaapos.2022.11.007
Autor:
Mariana Abi Karam, Arjun Sharma, Ashley Lopez-Canizares, Piero Carletti, Elizabeth A. Vanner, Audina M. Berrocal, Ta Chen Chang
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-6 (2024)
Abstract We conducted a retrospective review of patients (
Externí odkaz:
https://doaj.org/article/42d97a10645747d4a61a3786309ae9de
Autor:
Hasenin Al-khersan, Jesse Sengillo, Kenneth C. Fan, Ashley López-Cañizares, Natasha F.S. da Cruz, Nimesh A. Patel, Audina M. Berrocal
Publikováno v:
Ophthalmology Retina.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cc4265e1f55445a519b8371a04e761a2
https://doi.org/10.1016/j.oret.2023.02.005
https://doi.org/10.1016/j.oret.2023.02.005
Publikováno v:
Ophthalmic genetics.
Familial exudative vitreoretinopathy (FEVR) is a rare inherited disease characterized by abnormal retinal angiogenesis that leads to incomplete vascularization of the peripheral retina and ischemia. The disease demonstrates complex genetics and can b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23beec9e5c94ae43f73bc89a24981ef3
https://pubmed.ncbi.nlm.nih.gov/36444989
https://pubmed.ncbi.nlm.nih.gov/36444989
Autor:
Ashley López-Cañizares, Natasha Ferreira Santos da Cruz, Hasenin Al-khersan, Audina Maria Berrocal
Publikováno v:
Journal of VitreoRetinal Diseases. :247412642311732
Purpose: To present 2 cases of premature newborns with hyperbilirubinemia and retinopathy of prematurity (ROP) who could not be examined properly to assess for disease progression because of vitreous opacification in the setting of an icteric vitreou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::390f5e90172c0feeeb94d836e83c54c1
https://doi.org/10.1177/24741264231173206
https://doi.org/10.1177/24741264231173206
Autor:
Ashley López-Cañizares, Maria P. Fernandez, Hasenin Al-Khersan, Piero Carletti, Monica S Arroyo, Maria C Fernandez-Ruiz, Audina M Berrocal
Publikováno v:
Ophthalmic genetics. 43(4)
Coats plus syndrome or cerebroretinal microangiopathy with calcifications and cysts (CMCC) is an exceedingly rare autosomal recessive disorder that predominantly affects the microvasculature in the retina, brain, bones, and gastrointestinal system. U
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bf835fb80063281a412ef37388a0321
https://pubmed.ncbi.nlm.nih.gov/35416114
https://pubmed.ncbi.nlm.nih.gov/35416114
Publikováno v:
American Journal of Ophthalmology. 237:e1-e2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbbd1a7b2daaf2955232f469530e68f6
https://doi.org/10.1016/j.ajo.2021.12.013
https://doi.org/10.1016/j.ajo.2021.12.013
Autor:
Şengül Özdek, Ece Özdemir Zeydanlı, Caroline Baumal, Sandra Hoyek, Nimesh Patel, Audina Berrocal, Ashley Lopez-Cañizares, Hasenin Al-Khersan, Shunji Kusaka, Fukutaro Mano, Subhadra Jalali, Domenico Lepore, Solmaz Akar
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 53, Iss 1, Pp 44-57 (2023)
Avascular peripheral retina in an infant is a common characteristic of numerous pediatric retinal vascular disorders and often presents a diagnostic challenge to the clinician. In this review, key features of each disease in the differential diagnosi
Externí odkaz:
https://doaj.org/article/e34fe9325ef44aa3aafbd00b9fd0c6c0