Zobrazeno 1 - 10
of 283
pro vyhledávání: '"John H, Fingert"'
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 34, Iss , Pp 102020- (2024)
Purpose: To report a case of unsuccessful transscleral cyclophotocoagulation in a patient with OCA1A tyrosinase-negative oculocutaneous albinism. Observations: A 35-year-old Asian female with molecularly diagnosed OCA1A (tyrosinase-negative) oculocut
Externí odkaz:
https://doaj.org/article/29d9b779a1b44a909389bbe7436c5f91
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 29, Iss , Pp 101811- (2023)
Purpose: Alpha-gal syndrome (AGS) is an allergy to non-primate mammalian carbohydrate (galactose-alpha-1,3-galactose) which may cause anaphylaxis. Allergic patients must avoid ophthalmic drugs containing animal-derived ingredients. Observations: We r
Externí odkaz:
https://doaj.org/article/6c70fce31e424290a93e0c2cd2aed45c
Autor:
Carly van der Heide, Wes Goar, Kacie J. Meyer, Wallace L. M. Alward, Erin A. Boese, Nathan C. Sears, Ben R. Roos, Young H. Kwon, Adam P. DeLuca, Owen M. Siggs, Claudia Gonzaga-Jauregui, Val C. Sheffield, Kai Wang, Edwin M. Stone, Robert F. Mullins, Michael G. Anderson, Bao Jian Fan, Robert Ritch, Jamie E. Craig, Janey L. Wiggs, Todd E. Scheetz, John H. Fingert
Publikováno v:
BMC Genomics, Vol 22, Iss 1, Pp 1-12 (2021)
Abstract Background Glaucoma is a leading cause of visual disability and blindness. Release of iris pigment within the eye, pigment dispersion syndrome (PDS), can lead to one type of glaucoma known as pigmentary glaucoma. PDS has a genetic component,
Externí odkaz:
https://doaj.org/article/ce7f241b20c8405bb3d1d6a9635ffb16
Autor:
Joshua Hagedorn, Armin Avdic, Michael J. Schnieders, Benjamin R. Roos, Young H. Kwon, Arlene V. Drack, Erin A. Boese, John H. Fingert
Publikováno v:
BMC Ophthalmology, Vol 20, Iss 1, Pp 1-6 (2020)
Abstract Background Nanophthalmos has a significant genetic background and disease-causing mutations have been recently been reported in the myelin regulatory factor (MYRF) gene. We report clinical features in a patient with nanophthalmos and a Thr51
Externí odkaz:
https://doaj.org/article/a773c18c5d8f47cd81a2c7d263d78637
Autor:
Eileen S. Hwang, Denise J. Morgan, Katie L. Pennington, Leah A. Owen, John H. Fingert, Paul S. Bernstein, Margaret M. DeAngelis
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background We performed clinical and genetic characterization of a family with cavitary optic disc anomaly (CODA), an autosomal dominant condition that causes vision loss due to adult-onset maculopathy in the majority of cases. CODA is chara
Externí odkaz:
https://doaj.org/article/61cbe8d37a374580b439f92c0555cc3b
Autor:
Elliott H. Sohn, MD, Ian C. Han, MD, Benjamin R. Roos, BS, Benjamin Faga, BS, Meagan A. Luse, BS, Elaine M. Binkley, MD, H. Culver Boldt, MD, James C. Folk, MD, Stephen R. Russell, MD, Robert F. Mullins, PhD, John H. Fingert, MD, PhD, Edwin M. Stone, MD, PhD, Todd E. Scheetz, PhD
Publikováno v:
Ophthalmology Science, Vol 1, Iss 1, Pp 100002- (2021)
Purpose: To evaluate the first association specific to exudative age-related macular degeneration (AMD) located near the matrix metalloproteinase 9 (MMP9) gene. Design: Genetic association study. Participants: One thousand seven hundred twelve patien
Externí odkaz:
https://doaj.org/article/e464e9fd67834a58a547928b16aa7e00
Autor:
Natalie A. Afshari, Robert P. Igo, Nathan J. Morris, Dwight Stambolian, Shiwani Sharma, V. Lakshmi Pulagam, Steven Dunn, John F. Stamler, Barbara J. Truitt, Jacqueline Rimmler, Abraham Kuot, Christopher R. Croasdale, Xuejun Qin, Kathryn P. Burdon, S. Amer Riazuddin, Richard Mills, Sonja Klebe, Mollie A. Minear, Jiagang Zhao, Elmer Balajonda, George O. Rosenwasser, Keith H Baratz, V. Vinod Mootha, Sanjay V. Patel, Simon G. Gregory, Joan E. Bailey-Wilson, Marianne O. Price, Francis W. Price, Jamie E. Craig, John H. Fingert, John D. Gottsch, Anthony J. Aldave, Gordon K. Klintworth, Jonathan H. Lass, Yi-Ju Li, Sudha K. Iyengar
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-8 (2017)
Fuchs endothelial corneal dystrophy (FECD) is one of the most common reasons for corneal transplantation, and is known to cluster in families. Here, the authors discover new genetic loci associated with FECD with sex-specific effects and implications
Externí odkaz:
https://doaj.org/article/d1c65f3362014583bd22c5188abefc76
Autor:
Aminatta Z. Tejan-Kamara, Erin A. Boese, Andrew Pouw, Nathan C. Sears, Ben R. Roos, Edwin M. Stone, Todd, E. Scheetz, John H. Fingert
Publikováno v:
Ophthalmology Glaucoma.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9da9e5024ff6d70a6bd8ad1befd7730
https://doi.org/10.1016/j.ogla.2023.05.006
https://doi.org/10.1016/j.ogla.2023.05.006
Autor:
Andrew E. Pouw, Mark A. Greiner, Razek G. Coussa, Chunhua Jiao, Ian C. Han, Jessica M. Skeie, John H. Fingert, Robert F. Mullins, Elliott H. Sohn
Publikováno v:
Cells, Vol 10, Iss 3, p 687 (2021)
The extracellular matrix (ECM) plays a crucial role in all parts of the eye, from maintaining clarity and hydration of the cornea and vitreous to regulating angiogenesis, intraocular pressure maintenance, and vascular signaling. This review focuses o
Externí odkaz:
https://doaj.org/article/db438ca7772a4f05b2fe1a0596a72c79
Autor:
Inas F. Aboobakar, Tyler G. Kinzy, Yan Zhao, Baojian Fan, Louis R. Pasquale, Ayub Qassim, Antonia Kolovos, Joshua M. Schmidt, Jamie E. Craig, Jessica N. Cooke Bailey, Janey L. Wiggs, R. Rand Allingham, Murray Brilliant, Donald L. Budenz, John H. Fingert, Douglas Gaasterland, Teresa Gaasterland, Jonathan L. Haines, Michael A. Hauser, Richard K. Lee, Paul R. Lichter, Yutao Liu, Syoko Moroi, Jonathan Myers, Margaret Pericak-Vance, Anthony Realini, Doug Rhee, Julia E. Richards, Robert Ritch, Joel S. Schuman, William K. Scott, Kuldev Singh, Arthur J. Sit, Douglas Vollrath, Robert N. Weinreb, Gadi Wollstein, Donald J. Zack
Publikováno v:
Ophthalmology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50b0c1b32aaf70a4c50e834dbdee11c4
https://doi.org/10.1016/j.ophtha.2023.02.018
https://doi.org/10.1016/j.ophtha.2023.02.018