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TOMAS SANTIAGO ALEMAN MD
MD
Retina Specialist (Ophthalmology) Physician
NPI: 1104110303IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology Physician
Ophthalmology
Code: 207W00000X
MD449388(PA)
Retina Specialist (Ophthalmology) PhysicianPrimary
Ophthalmology — Retina Specialist
Code: 207WX0107X
MD449388(PA)
Education
OTHER
Class of 1988
Research & Publications (20)
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.
PMID 19578027·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
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutations.
PMID 18385078·Invest Ophthalmol Vis Sci·2008
4-observational
Macular pigment and lutein supplementation in ABCA4-associated retinal degenerations.
PMID 17325179·Invest Ophthalmol Vis Sci·2007
8-other
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.
PMID 17898302·Invest Ophthalmol Vis Sci·2007
8-other
Impairment of the transient pupillary light reflex in Rpe65(-/-) mice and humans with leber congenital amaurosis.
PMID 15037595·Invest Ophthalmol Vis Sci·2004
7-preclinical
Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotype.
PMID 12126946·Exp Eye Res·2002
8-other
Augmented rod bipolar cell function in partial receptor loss: an ERG study in P23H rhodopsin transgenic and aging normal rats.
PMID 11587727·Vision Res·2001
4-observational
Macular pigment and lutein supplementation in retinitis pigmentosa and Usher syndrome.
PMID 11431456·Invest Ophthalmol Vis Sci·2001
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
Leber congenital amaurosis caused by Lebercilin (LCA5) mutation: retained photoreceptors adjacent to retinal disorganization.
PMID 19503738·Mol Vis·2009
8-other
ABCA4 disease progression and a proposed strategy for gene therapy.
PMID 19074458·Hum Mol Genet·2009
8-other
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutations.
PMID 19117922·Invest Ophthalmol Vis Sci·2009
8-other
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
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.
PMID 19074810·Invest Ophthalmol Vis Sci·2009
8-other
Vision 1 year after gene therapy for Leber's congenital amaurosis.
PMID 19675341·N Engl J Med·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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3801 FILBERT ST
PHILADELPHIA, PA 19104 - Phone
- (215) 662-8100
Quick Facts
- NPI
- 1104110303
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 38
- Publications
- 20
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