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TERESA ALEMAN, PHARMD
PHARMD
Pharmacist
NPI: 1578984159Individual
Specialties, Licenses & Credentials
PharmacistPrimary
Pharmacist
Code: 183500000X
31467(FL)
Research & Publications (20)
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutations.
PMID 19117922·Invest Ophthalmol Vis Sci·2009
8-other
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic wavelets.
PMID 18704120·Eye (Lond)·2009
5-case
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.
PMID 19503738·Mol Vis·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
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·Invest Ophthalmol Vis Sci·2009
8-other
Harmonin in the murine retina and the retinal phenotypes of Ush1c-mutant mice and human USH1C.
PMID 19324851·Invest Ophthalmol Vis Sci·2009
7-preclinical
Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate.
PMID 19339306·Hum Mol Genet·2009
7-preclinical
ABCA4 disease progression and a proposed strategy for gene therapy.
PMID 19074458·Hum Mol Genet·2009
8-other
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
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
PMID 18463160·Hum Mol Genet·2008
7-preclinical
Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutations.
PMID 18539930·Invest Ophthalmol Vis Sci·2008
8-other
Treatment of leber congenital amaurosis due to RPE65 mutations by ocular subretinal injection of adeno-associated virus gene vector: short-term results of a phase I trial.
PMID 18774912·Hum Gene Ther·2008
3-trial
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
Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene.
PMID 18281613·Invest Ophthalmol Vis Sci·2008
8-other
Full-field stimulus testing (FST) to quantify visual perception in severely blind candidates for treatment trials.
PMID 17664667·Physiol Meas·2007
8-other
Human cone photoreceptor dependence on RPE65 isomerase.
PMID 17848510·Proc Natl Acad Sci U S A·2007
7-preclinical
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.
PMID 17898302·Invest Ophthalmol Vis Sci·2007
8-other
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosis.
PMID 17960108·Mol Vis·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 6201 N SUNCOAST BLVD
CRYSTAL RIVER, FL 34428 - Phone
- (352) 795-8360
Quick Facts
- NPI
- 1578984159
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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