Zobrazeno 1 - 10
of 431
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
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
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:
Morgan D. Basta, Svetlana Petruk, Ross Summer, Joel Rosenbloom, Peter J. Wermuth, Edward Macarak, Alex V. Levin, Alexander Mazo, Janice L. Walker
Publikováno v:
iScience, Vol 26, Iss 5, Pp 106570- (2023)
Summary: Cell reprogramming to a myofibroblast responsible for the pathological accumulation of extracellular matrix is fundamental to the onset of fibrosis. Here, we explored how condensed chromatin structure marked by H3K72me3 becomes modified to a
Externí odkaz:
https://doaj.org/article/ba372bd90ff342b6bee429d1eaefaafa
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:
Onochie Okoye, Jenina Capasso, Sarina M. Kopinsky, Louise Amlie‐Wolf, Alex V. Levin, Adele Schneider
Publikováno v:
American Journal of Medical Genetics Part A.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f334e527fc0b87e9a087d8817c915b2
https://doi.org/10.1002/ajmg.a.63239
https://doi.org/10.1002/ajmg.a.63239
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
Publikováno v:
American Journal of Medical Genetics Part A.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f36c4e98f513e2a5a7e00142d5b410a
https://doi.org/10.1002/ajmg.a.63191
https://doi.org/10.1002/ajmg.a.63191
Autor:
Amani Albakri, Phattrawan Pisuchpen, Jenina E. Capasso, Adele Schneider, Sarina Kopinsky, Tom Glaser, John P.‐W. Chiang, Anamaria Akapito Yomai, Donna McNear, Alex V. Levin
Publikováno v:
American journal of medical genetics. Part AREFERENCES.
The purpose of this article is to determine the cause of Leber congenital amaurosis (LCA) in Chuuk state, Federated States of Micronesia (FSM). In this prospective observational case series, five patients with early-onset vision loss were examined in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1eab36af6e18ed09ed7fed2d84538d4c
https://pubmed.ncbi.nlm.nih.gov/36595661
https://pubmed.ncbi.nlm.nih.gov/36595661