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SPENCER JACOBSON, DMD
DMD
Pediatric Dentistry
NPI: 1467149633Individual
Specialties, Licenses & Credentials
Pediatric DentistryPrimary
Dentist — Pediatric Dentistry
Code: 1223P0221X
7019303-9925(UT)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (20)
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.
PMID 19074810·Invest Ophthalmol Vis Sci·2009
8-other
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
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
Quantitative analysis of rest-activity patterns in elderly postoperative patients with delirium: support for a theory of pathologic wakefulness.
PMID 18468312·J Clin Sleep Med·2008
8-other
Co-transplantation of stromal cells interferes with the rejection of allogeneic islet grafts.
PMID 19120298·Ann N Y Acad Sci·2008
7-preclinical
Donepezil: potential neuroprotective and disease-modifying effects.
PMID 18798705·Expert Opin Drug Metab Toxicol·2008
6-review
Survey of vaccine distribution and delivery issues in the USA: from pediatrics to pandemics.
PMID 18377360·Expert Rev Vaccines·2007
6-review
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
An analysis of the pediatric vaccine supply shortage problem.
PMID 17186772·Health Care Manag Sci·2006
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
Chimeric peptide vaccine composed of B- and T-cell epitopes of human T-cell leukemia virus type 1 induces humoral and cellular immune responses and reduces the proviral load in immunized squirrel monkeys (Saimiri sciureus).
PMID 16603536·J Gen Virol·2006
7-preclinical
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration.
PMID 15229190·Hum Mol Genet·2004
4-observational
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination.
PMID 12700176·Hum Mol Genet·2003
8-other
Immunopathogenesis of human T cell lymphotropic virus type I-associated neurologic disease.
PMID 12424696·J Infect Dis·2002
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 575 S 200 E
HEBER CITY, UT 84032 - Phone
- (435) 315-3080
Quick Facts
- NPI
- 1467149633
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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