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Author Details
Full Name
Abigail T Fahim
Affiliation
University of Michigan (A.T.F.) ann arbor
ORCID
Career Start Year
2007
Papers
38
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36764426
Static Perimetry in the Rate of Progression in USH2A-related Retinal Degeneration (RUSH2A) Study: Assessment Through 2 Years.
Am J Ophthalmol
2023
37381907
Local progression kinetics of macular atrophy in recessive Stargardt disease.
Ophthalmic Genet
2023
35001204
Real-world outcomes of voretigene neparvovec treatment in pediatric patients with RPE65-associated Leber congenital amaurosis.
Graefes Arch Clin Exp Ophthalmol
2022
35644472
Automated Segmentation of Autofluorescence Lesions in Stargardt Disease.
Ophthalmol Retina
2022
36247208
Clinical and imaging findings of choroideremia in a pediatric patient due to a novel frameshift mutation.
Am J Ophthalmol Case Rep
2022
35882889
Oxidative stress differentially impacts apical and basolateral secretion of angiogenic factors from human iPSC-derived retinal pigment epithelium cells.
Sci Rep
2022
36007554
Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease Severity.
Am J Ophthalmol
2022
32507488
Coats-like Exudative Vitreoretinopathy in Retinitis Pigmentosa: Ocular Manifestations and Treatment Outcomes.
Ophthalmol Retina
2021
33662097
Association of No-Cost Genetic Testing Program Implementation and Patient Characteristics With Access to Genetic Testing for Inherited Retinal Degenerations.
JAMA Ophthalmol
2021
34185059
Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome.
Invest Ophthalmol Vis Sci
2021
33309692
The Michigan Vision-Related Anxiety Questionnaire: A Psychosocial Outcomes Measure for Inherited Retinal Degenerations.
Am J Ophthalmol
2021
32858027
The Michigan Retinal Degeneration Questionnaire: A Patient-Reported Outcome Instrument for Inherited Retinal Degenerations.
Am J Ophthalmol
2021
32566799
Rapid visual field constriction in a patient with retinitis pigmentosa and pituitary adenoma.
Am J Ophthalmol Case Rep
2020
31953110
X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa.
Ophthalmol Retina
2020
33133772
The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline.
Transl Vis Sci Technol
2020
32832209
Advancing Clinical Trials for Inherited Retinal Diseases: Recommendations from the Second Monaciano Symposium.
Transl Vis Sci Technol
2020
32865341
Genetic testing for inherited retinal degenerations: Triumphs and tribulations.
Am J Med Genet C Semin Med Genet
2020
32299429
Autoimmune retinopathy associated with monoclonal gammopathy of undetermined significance: a case report.
BMC Ophthalmol
2020
32400255
Cystoid macular edema precipitated by altitude in a patient with X-linked retinitis pigmentosa.
Ophthalmic Genet
2020
30979730
Detailed clinical characterisation, unique features and natural history of autosomal recessive <i>RDH12</i>-associated retinal degeneration.
Br J Ophthalmol
2019
31884613
Natural History and Genotype-Phenotype Correlations in RDH12-Associated Retinal Degeneration.
Adv Exp Med Biol
2019
28848025
Bullous X linked retinoschisis: clinical features and prognosis.
Br J Ophthalmol
2018
30234647
Retinitis pigmentosa: recent advances and future directions in diagnosis and management.
Curr Opin Pediatr
2018
30526558
Contrast sensitivity deficits in patients with mutation-proven inherited retinal degenerations.
BMC Ophthalmol
2018
28726568
Double hyperautofluorescent ring on fundus autofluorescence in ABCA4.
Ophthalmic Genet
2018
29038010
Peripheral Visual Fields in ABCA4 Stargardt Disease and Correlation With Disease Extent on Ultra-widefield Fundus Autofluorescence.
Am J Ophthalmol
2017
28348004
Peripheral fundus findings in X-linked retinoschisis.
Br J Ophthalmol
2017
27316272
Comparison of ophthalmic training in 6 English-speaking countries.
Can J Ophthalmol
2016
26427428
The Role of X-Chromosome Inactivation in Retinal Development and Disease.
Adv Exp Med Biol
2016
25375273
Understanding the adverse effects of ocriplasmin - reply.
JAMA Ophthalmol
2015
25996428
Acute ocriplasmin retinopathy.
Retina
2015
24577241
Acute panretinal structural and functional abnormalities after intravitreous ocriplasmin injection.
JAMA Ophthalmol
2014
24739995
Lateral geniculate lesions causing reversible blindness in a pre-eclamptic patient with a variant of posterior reversible encephalopathy syndrome.
J Neuroophthalmol
2014
23972307
Diagnostic fundus autofluorescence patterns in achromatopsia.
Am J Ophthalmol
2013
22183348
Polymorphic variation of RPGRIP1L and IQCB1 as modifiers of X-linked retinitis pigmentosa caused by mutations in RPGR.
Adv Exp Med Biol
2012
21857984
Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations.
PLoS One
2011
18774162
Transgenic overexpression of a stable Plasminogen Activator Inhibitor-1 variant.
Thromb Res
2009
18046404
A dual-Ca2+-sensor model for neurotransmitter release in a central synapse.
Nature
2007
1 - 38 of 38
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