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Full Name
Benjamin Bakall
Affiliation
University of Arizona College of Medicine
ORCID
Career Start Year
1996
Papers
30
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36249705
A Phase I, Single Ascending Dose Study of GEM103 (Recombinant Human Complement Factor H) in Patients with Geographic Atrophy.
Ophthalmol Sci
2022
30383557
CHOROIDAL NEOVASCULARIZATION IN NORTH CAROLINA MACULAR DYSTROPHY RESPONSIVE TO ANTI-VASCULAR ENDOTHELIAL GROWTH FACTOR THERAPY.
Retin Cases Brief Rep
2021
34895015
Best Vitelliform Macular Dystrophy (BVMD) is a phenocopy of North Carolina Macular Dystrophy (NCMD/MCDR1).
Ophthalmic Genet
2021
34584043
Genes and Gene Therapy in Inherited Retinal Disease.
Int Ophthalmol Clin
2021
34662339
Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis.
PLoS Genet
2021
34185059
Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome.
Invest Ophthalmol Vis Sci
2021
37009588
Retinal Manifestations of Incontinentia Pigmenti: A Case Series of 14 Patients Highlighting the Importance of Intravenous Fluorescein Angiography and the Benefits of Early Laser Photocoagulation.
J Vitreoretin Dis
2020
31067321
Indirect Traumatic Optic Neuropathy in Mild Chronic Traumatic Brain Injury.
Invest Ophthalmol Vis Sci
2019
31100169
Insights into Retinal Development Using Live Imaging in Female Carriers of Choroideremia.
Ophthalmic Surg Lasers Imaging Retina
2019
31047589
Extensive Grouped Congenital Hypertrophy of the Retinal Pigment Epithelium.
Ophthalmol Retina
2018
30021033
Emerging Gene Therapy Treatments for Inherited Retinal Diseases.
Ophthalmic Surg Lasers Imaging Retina
2018
28586915
Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy.
Invest Ophthalmol Vis Sci
2017
28095098
Reduced penetrance in a large Caucasian pedigree with Stickler syndrome.
Ophthalmic Genet
2017
26980447
Treatment of vitamin A deficiency retinopathy with sublingual vitamin A palmitate.
Doc Ophthalmol
2016
26858522
Comparison of microbiology and visual outcomes of patients undergoing small-gauge and 20-gauge vitrectomy for endophthalmitis.
Clin Ophthalmol
2016
25764055
Autosomal Dominant Microcephaly Associated With Congenital Lymphedema and Chorioretinopathy Due to a Novel Mutation in KIF11.
JAMA Ophthalmol
2015
23706500
Aflibercept therapy for exudative age-related macular degeneration resistant to bevacizumab and ranibizumab.
Am J Ophthalmol
2013
23918662
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease.
Hum Mol Genet
2013
23209588
Retinal vessel width measurement at branchings using an improved electric field theory-based graph approach.
PLoS One
2012
18385076
Bestrophin-2 is involved in the generation of intraocular pressure.
Invest Ophthalmol Vis Sci
2008
17477921
Enhanced accumulation of A2E in individuals homozygous or heterozygous for mutations in BEST1 (VMD2).
Exp Eye Res
2007
17872905
Lack of fibulin-3 causes early aging and herniation, but not macular degeneration in mice.
Hum Mol Genet
2007
16282372
Expression of bestrophin-1, the product of the VMD2 gene, modulates voltage-dependent Ca2+ channels in retinal pigment epithelial cells.
FASEB J
2006
15452084
A model of best vitelliform macular dystrophy in rats.
Invest Ophthalmol Vis Sci
2004
12882816
Expression and localization of bestrophin during normal mouse development.
Invest Ophthalmol Vis Sci
2003
11449320
Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene.
Ophthalmic Genet
2001
10617923
Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene.
Ophthalmic Genet
1999
10394929
The mutation spectrum of the bestrophin protein--functional implications.
Hum Genet
1999
9662395
Identification of the gene responsible for Best macular dystrophy.
Nat Genet
1998
8941270
Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism.
Muscle Nerve
1996
1 - 30 of 30
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