Zobrazeno 1 - 10
of 303
pro vyhledávání: '"Byron L. Lam"'
Autor:
Neil Dogra, Bryan V. Redmond, Selena Lilley, Brent A. Johnson, Byron L. Lam, Madhura Tamhankar, Steven E. Feldon, Berkeley Fahrenthold, Jingyi Yang, Krystel R. Huxlin, Matthew R. Cavanaugh
Publikováno v:
Brain and Behavior, Vol 14, Iss 7, Pp n/a-n/a (2024)
Background/objectives Stroke damage to the primary visual cortex induces large, homonymous visual field defects that impair daily living. Here, we asked if vision‐related quality of life (VR‐QoL) is impacted by time since stroke. Subjects/methods
Externí odkaz:
https://doaj.org/article/fb0d09891f53462ebe31e363bff10ac9
Autor:
Alcina K. Lidder, Stephanie Choi, Yasha S. Modi, Scott E. Brodie, Janet L. Davis, Ninel Z. Gregori, Byron L. Lam
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 32, Iss , Pp 101879- (2023)
Purpose: To report panuveitis with exudative retinal detachments in a healthy 27-year-old woman with biallelic mutations in the RPE65 gene, who underwent bilateral sequential gene therapy with subretinal administration of voretigene neparvovec-rzyl.
Externí odkaz:
https://doaj.org/article/05675087d50e47d2afc8f087a3df93aa
Autor:
Jeffrey L. Goldberg, MD, PhD, Gala Beykin, MD, Kellie R. Satterfield, MD, Mariana Nuñez, MD, Byron L. Lam, MD, Thomas A. Albini, MD
Publikováno v:
Ophthalmology Science, Vol 3, Iss 3, Pp 100298- (2023)
Purpose: To assess the safety and efficacy of a ciliary neurotrophic factor (CNTF) intraocular implant on neuroprotection and neuroenhancement in glaucoma. Design: Open-label, prospective, phase I clinical trial. Participants: A total of 11 participa
Externí odkaz:
https://doaj.org/article/fa60a287ea4c44debc2a1ecc822aaf44
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 16, p 5283 (2023)
Patients with inherited retinal diseases (IRDs) utilize various adaptive techniques and devices designed to assist them with activities of daily living (ADLs). The purpose of this study was to assess the assistive devices used by patients with IRDs,
Externí odkaz:
https://doaj.org/article/c021d6a15d5641bdbd8468084cdcb082
Bilateral visual acuity decline in males with choroideremia: a pooled, cross-sectional meta-analysis
Publikováno v:
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background Choroideremia is a rare inherited retinal disease that leads to blindness. Visual acuity (VA) is a key outcome measure in choroideremia treatment studies, but VA decline rates change with age. An accurate understanding of the natu
Externí odkaz:
https://doaj.org/article/bb7f5a30ed944b959b10182f1d5d5b4b
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Inherited retinal diseases (IRDs) are a diverse group of degenerative diseases of the retina that can lead to significant reduction in vision and blindness. Because of the considerable phenotypic overlap among IRDs, genetic testing is a crit
Externí odkaz:
https://doaj.org/article/09140c70eb264a5a81b1f593ce4048e3
Autor:
Aniz Girach, Isabelle Audo, David G. Birch, Rachel M. Huckfeldt, Byron L. Lam, Bart P. Leroy, Michel Michaelides, Stephen R. Russell, Juliana M.F. Sallum, Katarina Stingl, Stephen H. Tsang, Paul Yang
Publikováno v:
Therapeutic Advances in Ophthalmology, Vol 14 (2022)
Inherited retinal diseases (IRDs) are a genetically and phenotypically heterogeneous group of genetic eye disorders. There are more than 300 disease entities, and together this group of disorders affects millions of people globally and is a frequent
Externí odkaz:
https://doaj.org/article/226aab6d39cd48b586763105aaa823da
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 25, Iss , Pp 101253- (2022)
Purpose: To report a unique case of metastatic paraganglioma presenting as a junctional scotoma. Observations: A 38-year-old Caucasian man with a history of abdominal paraganglioma presented with minimally blurred vision 20/25 visual acuity in the le
Externí odkaz:
https://doaj.org/article/93237df0786f49bc9e269ad4d42032e8
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 19, Iss , Pp 100862- (2020)
Purpose: To report diagnostic and management challenges of a case of WHO Grade III glioma of the optic nerve occurring in an unusually young patient with more than 7 years of survival without recurrence. Observations: An 18-year-old woman reported ra
Externí odkaz:
https://doaj.org/article/675df60b9e764ec7a314158bece952a4
Autor:
Evan M. de Joya, Brett M. Colbert, Pei-Ciao Tang, Byron L. Lam, Jun Yang, Susan H. Blanton, Derek M. Dykxhoorn, Xuezhong Liu
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 8, p 3910 (2021)
Hearing loss is the most common sensory disorder with ~466 million people worldwide affected, representing about 5% of the population. A substantial portion of hearing loss is genetic. Hearing loss can either be non-syndromic, if hearing loss is the
Externí odkaz:
https://doaj.org/article/c4c22776b7b64411855d3c2dc8faf365