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Author Details
Full Name
Byron L Lam
Affiliation
Bascom Palmer Eye Institute
ORCID
Career Start Year
1986
Papers
274
H Index
44
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36000786
Severe Vision Loss and Optic Disc Edema Associated With GAD-65 Antibody Positive Miller Fisher Syndrome.
J Neuroophthalmol
2024
37716450
Leber Hereditary Optic Neuropathy Gene Therapy: Longitudinal Relationships Among Visual Function and Anatomical Measures.
Am J Ophthalmol
2024
37575054
Choroideremia presenting as vision loss secondary to choroidal neovascularization.
Ophthalmic Genet
2024
36757689
Changes in Retinal Sensitivity Associated With Cotoretigene Toliparvovec in X-Linked Retinitis Pigmentosa With RPGR Gene Variations.
JAMA Ophthalmol
2023
37629325
Current Assistive Devices Usage and Recommendations for a Future Artificial Vision Prosthesis among Patients with Severe Visual Impairment Due to Inherited Retinal Diseases.
J Clin Med
2023
37521805
Bilateral exudative retinal detachments after subretinal gene therapy with voretigene neparvovec-rzyl for RPE65 Leber Congenital Amaurosis.
Am J Ophthalmol Case Rep
2023
37284436
Sirolimus Induced Toxic Optic Neuropathy.
Int Med Case Rep J
2023
37404515
Thrombosed orbital varix of the inferior ophthalmic vein: A rare cause of acute unilateral proptosis.
Surg Neurol Int
2023
37197702
Phase I NT-501 Ciliary Neurotrophic Factor Implant Trial for Primary Open-Angle Glaucoma: Safety, Neuroprotection, and Neuroenhancement.
Ophthalmol Sci
2023
36965511
When my green eye turns brown: transient monocular heterochromia and vision loss due to uveitis-glaucoma-hyphema syndrome.
Can J Ophthalmol
2023
34001730
Cavernous Malformation of the Optic Nerve and Chiasm: Prompt Suspicion and Surgery Matter.
J Neuroophthalmol
2022
35377395
Association of Maintenance Intravenous Immunoglobulin With Prevention of Relapse in Adult Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.
JAMA Neurol
2022
35344016
The Relationship Between Stage of Leber's Hereditary Optic Neuropathy and Pattern Electroretinogram Latency.
Transl Vis Sci Technol
2022
35483032
SWEPT-SOURCE OPTICAL COHERENCE TOMOGRAPHY DETECTION OF BRUCH MEMBRANE AND CHORIOCAPILLARIS ABNORMALITIES IN SORSBY MACULAR DYSTROPHY.
Retina
2022
36388727
RNA-based therapies in inherited retinal diseases.
Ther Adv Ophthalmol
2022
35034620
Bilateral visual acuity decline in males with choroideremia: a pooled, cross-sectional meta-analysis.
BMC Ophthalmol
2022
35271811
Leber Hereditary Optic Neuropathy Gene Therapy: Adverse Events and Visual Acuity Results of All Patient Groups.
Am J Ophthalmol
2022
34896323
Visual Acuity, Retinal Morphology, and Patients' Perceptions after Voretigene Neparovec-rzyl Therapy for RPE65-Associated Retinal Disease.
Ophthalmol Retina
2022
34039936
Review of Genotype-Phenotype Correlations in Usher Syndrome.
Ear Hear
2022
32441142
Non-invasive Assessment of Central Retinal Artery Pressure: Age and Posture-dependent Changes.
Curr Eye Res
2021
33595255
LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS-SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED: A Review.
Retina
2021
33510950
Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia.
Transl Vis Sci Technol
2021
33920085
Usher Syndrome in the Inner Ear: Etiologies and Advances in Gene Therapy.
Int J Mol Sci
2021
35036631
Metastatic paraganglioma presenting as ajunctional scotoma.
Am J Ophthalmol Case Rep
2021
35002221
Analysis of Socioeconomic Factors Affecting Follow-Up in a Glaucoma Screening Program.
Clin Ophthalmol
2021
34906171
Genetic testing and diagnosis of inherited retinal diseases.
Orphanet J Rare Dis
2021
34584056
Choroideremia Gene Therapy.
Int Ophthalmol Clin
2021
34223797
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome.
Ophthalmic Genet
2021
34185059
Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome.
Invest Ophthalmol Vis Sci
2021
34154722
En Face Widefield OCT Angiography of MEK Inhibitor-Associated Retinopathy.
Ophthalmology
2021
34111268
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure.
Transl Vis Sci Technol
2021
33242498
Efficacy of Visual Retraining in the Hemianopic Field after Stroke: Results of a Randomized Clinical Trial.
Ophthalmology
2021
33471812
Multimorbidity patterns and their relationship to mortality in the US older adult population.
PLoS One
2021
32956221
Erdheim-Chester Disease Presenting With Diplopia: A Challenging Diagnosis With Effective Treatment.
J Neuroophthalmol
2021
31568904
Imaging Characteristics of a Hypervascular Pituitary Spindle Cell Oncocytoma on Magnetic Resonance Imaging and Digital Subtraction Angiography.
World Neurosurg
2020
32105300
Patterns of Chronic Conditions and Their Association With Visual Impairment and Health Care Use.
JAMA Ophthalmol
2020
33262662
Sixth Cranial Nerve Palsy as the Presenting Sign of Metastatic Cholangiocarcinoma.
Int Med Case Rep J
2020
32875146
Malignant optic nerve glioma in a young woman with 7 year follow up without recurrence.
Am J Ophthalmol Case Rep
2020
32955497
Electroretinogram Recording for Infants and Children under Anesthesia to Achieve Optimal Dark Adaptation and International Standards.
J Vis Exp
2020
32554760
Steroid-sparing maintenance immunotherapy for MOG-IgG associated disorder.
Neurology
2020
32360766
Chronic condition patterns in the US population and their association with health related quality of life.
Prev Med
2020
32244898
A2E Distribution in RPE Granules in Human Eyes.
Molecules
2020
32108519
Interocular Symmetry of Foveal Cone Topography in Congenital Achromatopsia.
Curr Eye Res
2020
32124668
X-linked peripheral retinoschisis without macular involvement: a case series with <i>RS1</i> genetic confirmation.
Ophthalmic Genet
2020
28426632
Intraoperative Use of Microscope-Integrated Optical Coherence Tomography for Subretinal Gene Therapy Delivery.
Retina
2019
31645983
A founder deletion in the <i>TRPM1</i> gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews.
Hum Genome Var
2019
30240725
Choroideremia Gene Therapy Phase 2 Clinical Trial: 24-Month Results.
Am J Ophthalmol
2019
31335483
Surgical Technique for Subretinal Gene Therapy in Humans with Inherited Retinal Degeneration.
Retina
2019
31145438
Successes and Challenges of Retinal Implants for Profound Visual Loss From Outer Retinal Degeneration.
JAMA Ophthalmol
2019
30297337
Macular spatial distribution of preserved autofluorescence in patients with choroideremia.
Br J Ophthalmol
2019
1 - 50 of 274
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Lee M Jampol
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Robert Ritch
Einhorn Clinical Research Center, New York Eye and Ear Infirmary of Mount Sinai
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row(s) 1 - 30 of 30
Collaborators
David J Lee
University of Miami Miller School of Medicine.
Co-authored papers
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Co-authored papers
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Co-authored papers
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Giovanni Gregori
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Samuel G Jacobson
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Co-authored papers
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Richard G Weleber
Casey Eye Institute, Oregon Health & Science University
Co-authored papers
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Val C Sheffield
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Co-authored papers
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Philip J Rosenfeld
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Joseph Carroll
Medical College of Wisconsin Eye Institute
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Michel Michaelides
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Bonnielin K Swenor
Johns Hopkins Disability Health Research Center, Johns Hopkins University
Co-authored papers
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Sheila K West
Wilmer Eye Institute, Johns Hopkins University (S.W.
Co-authored papers
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Andrew R Webster
Institute of Ophthalmology, University College London
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Robert F Mullins
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Michael B Gorin
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