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ERIC WINDSOR, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1699359901Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Vision 1 year after gene therapy for Leber's congenital amaurosis.
PMID 19675341·N Engl J Med·2009
5-case
Human RPE65 gene therapy for Leber congenital amaurosis: persistence of early visual improvements and safety at 1 year.
PMID 19583479·Hum Gene Ther·2009
3-trial
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·Invest Ophthalmol Vis Sci·2009
8-other
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.
PMID 19503738·Mol Vis·2009
8-other
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutations.
PMID 19117922·Invest Ophthalmol Vis Sci·2009
8-other
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.
PMID 19074810·Invest Ophthalmol Vis Sci·2009
8-other
ABCA4 disease progression and a proposed strategy for gene therapy.
PMID 19074458·Hum Mol Genet·2009
8-other
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic wavelets.
PMID 18704120·Eye (Lond)·2009
5-case
Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.
PMID 18281613·Invest Ophthalmol Vis Sci·2008
8-other
Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutations.
PMID 18539930·Invest Ophthalmol Vis Sci·2008
8-other
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations.
PMID 18385078·Invest Ophthalmol Vis Sci·2008
4-observational
Human gene therapy for RPE65 isomerase deficiency activates the retinoid cycle of vision but with slow rod kinetics.
PMID 18809924·Proc Natl Acad Sci U S A·2008
3-trial
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.
PMID 17898302·Invest Ophthalmol Vis Sci·2007
8-other
Human cone photoreceptor dependence on RPE65 isomerase.
PMID 17848510·Proc Natl Acad Sci U S A·2007
7-preclinical
Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis.
PMID 17554762·Hum Mutat·2007
7-preclinical
Macular pigment and lutein supplementation in ABCA4-associated retinal degenerations.
PMID 17325179·Invest Ophthalmol Vis Sci·2007
8-other
RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expression.
PMID 17197551·Invest Ophthalmol Vis Sci·2007
8-other
Retinal disease expression in Bardet-Biedl syndrome-1 (BBS1) is a spectrum from maculopathy to retina-wide degeneration.
PMID 17065520·Invest Ophthalmol Vis Sci·2006
8-other
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutations.
PMID 16936131·Invest Ophthalmol Vis Sci·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 450 CLARKSON AVENUE, MSC 30, DEPARTMENT OF ORTHOPAEDIC SURGERY
BROOKLYN, NY 11203 - Phone
- (718) 270-2045
Quick Facts
- NPI
- 1699359901
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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