Back to Search
ELISA BERSON, MD
MD
Student in an Organized Health Care Education/Training Program
NPI: 1508568619Individual
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)
Progressive hydroxychloroquine toxicity mimicking low-tension glaucoma after discontinuation of the drug.
PMID 18937815·Acta Ophthalmol·2010
5-case
Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutation.
PMID 19325938·Mol Vis·2009
8-other
A single-base substitution within an intronic repetitive element causes dominant retinitis pigmentosa with reduced penetrance.
PMID 19618371·Hum Mutat·2009
8-other
A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosa.
PMID 19074801·Invest Ophthalmol Vis Sci·2009
8-other
Sessions 3 and 8: pretreatment and biomass recalcitrance: fundamentals and progress.
PMID 19322524·Appl Biochem Biotechnol·2009
8-other
Visual acuity is related to parafoveal retinal thickness in patients with retinitis pigmentosa and macular cysts.
PMID 18552390·Invest Ophthalmol Vis Sci·2008
8-other
Disease course in patients with autosomal recessive retinitis pigmentosa due to the USH2A gene.
PMID 18641288·Invest Ophthalmol Vis Sci·2008
8-other
Insights from retinitis pigmentosa into the roles of isocitrate dehydrogenases in the Krebs cycle.
PMID 18806796·Nat Genet·2008
4-observational
Premature termination codons in PRPF31 cause retinitis pigmentosa via haploinsufficiency due to nonsense-mediated mRNA decay.
PMID 18317597·J Clin Invest·2008
8-other
Disease course of patients with X-linked retinitis pigmentosa due to RPGR gene mutations.
PMID 17325176·Invest Ophthalmol Vis Sci·2007
8-other
Long-term visual prognoses in patients with retinitis pigmentosa: the Ludwig von Sallmann lecture.
PMID 17531222·Exp Eye Res·2007
8-other
Novel mutations in the KCNV2 gene in patients with cone dystrophy and a supernormal rod electroretinogram.
PMID 17896311·Ophthalmic Genet·2007
8-other
Low prevalence of lecithin retinol acyltransferase mutations in patients with Leber congenital amaurosis and autosomal recessive retinitis pigmentosa.
PMID 17438524·Mol Vis·2007
8-other
Natural course of ocular function in pigmented paravenous retinochoroidal atrophy.
PMID 16564825·Am J Ophthalmol·2006
8-other
Mutation screening of the peropsin gene, a retinal pigment epithelium specific rhodopsin homolog, in patients with retinitis pigmentosa and allied diseases.
PMID 17167409·Mol Vis·2006
8-other
Variation in retinitis pigmentosa-11 (PRPF31 or RP11) gene expression between symptomatic and asymptomatic patients with dominant RP11 mutations.
PMID 16708387·Hum Mutat·2006
4-observational
Rod and cone opsin mislocalization in an autopsy eye from a carrier of X-linked retinitis pigmentosa with a Gly436Asp mutation in the RPGR gene.
PMID 16935610·Am J Ophthalmol·2006
8-other
A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosa.
PMID 17167406·Mol Vis·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
- 5323 HARRY HINES BLVD STOP 7200
DALLAS, TX 75390 - Phone
- (214) 648-3111
Quick Facts
- NPI
- 1508568619
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile