Back to Search
SARA JACOBSON, M.D.
M.D.
Pediatrics Physician
NPI: 1861450785Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
227551(MA)
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
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutations.
PMID 16936131·Invest Ophthalmol Vis Sci·2006
8-other
Safety of recombinant adeno-associated virus type 2-RPE65 vector delivered by ocular subretinal injection.
PMID 16644289·Mol Ther·2006
7-preclinical
Identifying photoreceptors in blind eyes caused by RPE65 mutations: Prerequisite for human gene therapy success.
PMID 15837919·Proc Natl Acad Sci U S A·2005
7-preclinical
Focused cervical exploration for primary hyperparathyroidism without intraoperative parathyroid hormone monitoring or use of the gamma probe.
PMID 15490069·World J Surg·2004
8-other
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration.
PMID 15229190·Hum Mol Genet·2004
4-observational
Molecular requirements for gene expression mediated by targeted histone acetyltransferases.
PMID 15199156·Mol Cell Biol·2004
8-other
Psychiatric perspectives on headache and facial pain.
PMID 15025016·Otolaryngol Clin North Am·2003
6-review
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination.
PMID 12700176·Hum Mol Genet·2003
8-other
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophy.
PMID 11879143·Arch Ophthalmol·2002
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
- 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
Are you this provider?
Claim Your Profile