Zobrazeno 1 - 10
of 398
pro vyhledávání: '"Alex V Levin"'
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 13, Iss 4, Pp 500-504 (2023)
The anterior segment dysgeneses are a broad group of heterogeneous disorders characterized by developmental abnormalities of the anterior segment of the eye, including primary congenital aphakia, Peters sequence, aniridia, and Axenfeld–Rieger spect
Externí odkaz:
https://doaj.org/article/1adacfcb899847a9b379ddc7047fe7d0
Autor:
Diego I Paredes, Lorena M Haefeli, Onochie Okoye, Jenina E Capasso, Celeste Wyman, Vikas Khetan, Alex V Levin
Publikováno v:
Oman Journal of Ophthalmology, Vol 16, Iss 1, Pp 1-3 (2023)
Externí odkaz:
https://doaj.org/article/20342352dd914e939aea0cdd8bb704f5
Autor:
Wadakarn Wuthisiri, Yu-Hung Lai, Jenina Capasso, Martin Blidner, David Salz, Erik Kruger, Alex V Levin
Publikováno v:
Taiwan Journal of Ophthalmology, Vol 7, Iss 3, Pp 172-176 (2017)
Visual loss in systemic lupus erythematosus (SLE) due to autoimmune retinopathy (AIR) is rare and easily misdiagnosed as hydroxychloroquine retinopathy. We report the rare clinical presentation of severe visual loss in a patient with SLE due to nonpa
Externí odkaz:
https://doaj.org/article/3d766ed105464429bf65e19a9e57fca5
Autor:
Thales A. C De Guimarães, Jenina E Capasso, Nicholas R Bello, Nutsuchar Wangtiraumnuay, Michelle D Lingao, Wadakarn Wuthisiri, Yu-Hung Lai, Erica S Johnson, Mario Zanolli, Vikas Khetan, Renu Bajaj, Zi-Xuan Wang, Stephen C Peiper, Alex V Levin
Publikováno v:
The Pan-American Journal of Ophthalmology, Vol 3, Iss 1, Pp 10-10 (2021)
Introduction: The etiologies of congenital and developmental cataracts are diverse. Most are not syndromic and have no identifiable cause, thus creating a diagnostic dilemma. We investigated the utility of chromosomal microarray in identifying the et
Externí odkaz:
https://doaj.org/article/fd3b63abdfa047ddbf7c19b4cde36fc1
Autor:
Vikas Khetan, Mario Zanolli, Jenina Capasso, Nanette Zale Refice, Kimberley Neeley, Alex V Levin
Publikováno v:
Indian Journal of Ophthalmology, Vol 64, Iss 5, Pp 399-402 (2016)
In this communication, we report the case of a four year old boy who presented with reduced vision in the right eye. He had visual acuity of light perception right eye and 6/12 in the left eye and anterior segment examination was normal. Fundus exami
Externí odkaz:
https://doaj.org/article/05aaaa3dab364a80b8702b5a59e24bf1
Autor:
Hang Pham, Michelle D Lingao, Anuradha Ganesh, Jenina E Capasso, Rosanne Keep, Karthikeyan A Sadagopan, Alex V Levin
Publikováno v:
Oman Journal of Ophthalmology, Vol 9, Iss 1, Pp 49-51 (2016)
Organophosphates have rarely been reported to cause various ocular sequelae including retinal degeneration. Retinal manifestations have been rarely reported and poorly characterized. We describe a case of a 76-year-old man with vision loss beginning
Externí odkaz:
https://doaj.org/article/36308fee02d245f5a0d21de7d359aecc
Publikováno v:
Oman Journal of Ophthalmology, Vol 5, Iss 3, Pp 144-149 (2012)
The eye has played a major role in human genomics including gene therapy. It is the fourth most common organ system after integument (skin, hair and nails), nervous system, and musculoskeletal system to be involved in genetic disorders. The eye is in
Externí odkaz:
https://doaj.org/article/19514062d5694c58b90e1e57ae92147d
Publikováno v:
Oman Journal of Ophthalmology, Vol 6, Iss 3, Pp 203-205 (2013)
The purpose of this study is to describe transient macular cysts in an infant and correlate their occurrence with normal development events. A newborn Caucasian girl presented with a protruding corneal mass in her left eye at birth. She underwent a c
Externí odkaz:
https://doaj.org/article/083c61b20bfd4765860df171cc700c41
Autor:
Alex V Levin
Publikováno v:
Oman Journal of Ophthalmology, Vol 3, Iss 2, Pp 49-50 (2010)
Externí odkaz:
https://doaj.org/article/0000793345fe4ce6a80a6be04f29a003
Highly Commended by the BMA Medical Book Awards for Surgical Specialties!Many serious, potentially blinding eye disorders have a genetic basis. Currently, there are relatively few ocular geneticists in the world, yet inherited eye disease is one of t
