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SARA JACOBSON, M.D.
M.D.
Pediatrics Physician
NPI: 1861450785Individual
Specialties, Licenses & Credentials
Research & Publications (20)
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
Photoreceptor layer topography in children with leber congenital amaurosis caused by RPE65 mutations.
PMID 18539930·Invest Ophthalmol Vis Sci·2008
8-other
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
PMID 18463160·Hum Mol Genet·2008
7-preclinical
Pyoderma gangrenosum following tattoo placement in a patient with acute myelogenous leukemia.
PMID 18273727·J Dermatolog Treat·2008
5-case
Human cone photoreceptor dependence on RPE65 isomerase.
PMID 17848510·Proc Natl Acad Sci U S A·2007
7-preclinical
Leber congenital amaurosis caused by an RPGRIP1 mutation shows treatment potential.
PMID 17306875·Ophthalmology·2007
5-case
RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expression.
PMID 17197551·Invest Ophthalmol Vis Sci·2007
8-other
Safety in nonhuman primates of ocular AAV2-RPE65, a candidate treatment for blindness in Leber congenital amaurosis.
PMID 16942444·Hum Gene Ther·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
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Contact & Hours
- Address
- 105 MILLBURY ST
AUBURN, MA 01501 - Phone
- (508) 832-9691
Quick Facts
- NPI
- 1861450785
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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