Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Keri F. Allen"'
Autor:
W T Allison, Louis R. Pasquale, Michael A. Walter, Baojian Fan, Janey L. Wiggs, Tim Footz, David S. Greenfield, Keri F. Allen, Jamie E Craig, Robert Ritch, Gavin J. Neil, Richard K. Parrish, Kevin Linkroum, Kim Nguyen-Phuoc, Ordan J. Lehmann, Adrian Lahola-Chomiak, Shari Javadiyan, Ralf M. Leonhardt
Pigmentary glaucoma (PG) is a common glaucoma subtype that results from release of pigment from the iris, called pigment dispersion syndrome (PDS), and its deposition throughout the anterior chamber of the eye. Although PG has a substantial heritable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33ecf4fc521eac654a26164db4f6c7b2
https://europepmc.org/articles/PMC6452206/
https://europepmc.org/articles/PMC6452206/
Autor:
John F. Payne, W. Lloyd Clark, Beau B. Bruce, Charles C. Wykoff, David M. Brown, Brandon M. Menke, Shawn M. Iverson, Keri F. Allen, David S. Boyer, John A. Wells, David L. Johnson, Matthew Benz, Eric Chen, Richard H. Fish, Rosa Y. Kim, James C. Major, Ronan E. O’Malley, Amy C. Schefler, Ankoor R. Shah, Tien P. Wong, Roger L. Novack, Thomas G. Chu, Firas Rahhal, Homayoun Tabandeh, Richard H. Roe, Pouya N. Dayani, David Liao, Alexander Walsh, Daniel D. Esmaili
Publikováno v:
Ophthalmology. 125(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::504a698d93ad6a66ce5890e19016d724
https://pubmed.ncbi.nlm.nih.gov/29729809
https://pubmed.ncbi.nlm.nih.gov/29729809
Autor:
Eric D, Gaier, Katherine, Boudreault, Isao, Nakata, Maria, Janessian, Philip, Skidd, Elizabeth, DelBono, Keri F, Allen, Louis R, Pasquale, Emily, Place, Dean M, Cestari, Rebecca C, Stacy, Joseph F, Rizzo, Janey L, Wiggs
Publikováno v:
Molecular Vision
Purpose Inherited optic neuropathy is genetically heterogeneous, and genetic testing has an important role in risk assessment and counseling. The purpose of this study is to determine the prevalence and spectrum of mutations in a group of patients re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad8f354792833b02b842d110bc93c977
https://pubmed.ncbi.nlm.nih.gov/28848318
https://pubmed.ncbi.nlm.nih.gov/28848318
Autor:
Francesca Pasutto, Steve Rozen, Keri F. Allen, Terri L. Young, Shahrbanou Javadiyan, Tiger Zhou, Tomokazu Souma, Stuart W. Tompson, Kathryn P. Burdon, Kristina N. Whisenhunt, Simone Finzi, Khanh Nhat Tran-Viet, Shinji Yamaguchi, David A. Mackey, Jing Jin, Dimitar N. Azmanov, Sing Hui Lim, Sebastian Maurer-Stroh, Bethany A. Kloss, Alex W. Hewitt, Jonathan B Ruddle, Janey L. Wiggs, Krishnakumar Kizhatil, Jamie E Craig, Benjamin R. Thomson, Emmanuelle Souzeau, Susan E. Quaggin, Luba Kalaydjieva, Simon W. M. John, Xiaorong Liu, Vachiranee Limviphuvadh, Lucia Mauri, Owen M. Siggs, Tammy L. Yanovitch, Liang Feng
Publikováno v:
The Journal of clinical investigation. 126(7)
Primary congenital glaucoma (PCG) is a devastating eye disease and an important cause of childhood blindness worldwide. In PCG, defects in the anterior chamber aqueous humor outflow structures of the eye result in elevated intraocular pressure (IOP);
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fdc4703ba7fd7930ce3ff130d9e61b1
https://pubmed.ncbi.nlm.nih.gov/27270174
https://pubmed.ncbi.nlm.nih.gov/27270174
Publikováno v:
Transactions of the American Ophthalmological Society. 112
CYP1B1 mutations cause autosomal recessive congenital glaucoma. Disease risk assessment for families with CYP1B1 mutations requires knowledge of the population mutation carrier frequency. The purpose of this study is to determine the CYP1B1 mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4cda4cabbf212e62cb80353409eb057a
https://pubmed.ncbi.nlm.nih.gov/25646030
https://pubmed.ncbi.nlm.nih.gov/25646030
Publikováno v:
Cold Spring Harbor Perspectives in Medicine. 5:a017277
Inherited disorders of the optic nerve significantly impact vision in children and adults. The optic nerve disorders most commonly encountered clinically are glaucoma and primary optic neuropathy including Leber's hereditary optic neuropathy (LHON) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a167876532ce180c932a7fce9e92243c
https://doi.org/10.1101/cshperspect.a017277
https://doi.org/10.1101/cshperspect.a017277