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DAVID SAPERSTEIN, DO
DO
Body Imaging Physician
NPI: 1992876973IndividualAccepts Medicare
Specialties, Licenses & Credentials
Body Imaging PhysicianPrimary
Radiology — Body Imaging
Code: 2085B0100X
20A4197(CA)
CMS Specialties
PrimaryINTERVENTIONAL RADIOLOGY
Education
CHICAGO COLLEGE OF OSTEOPATHY
Class of 1968
Research & Publications (20)
Challenges in the identification of cobalamin-deficiency polyneuropathy.
PMID 12975298·Arch Neurol·2003
8-other
Current concepts and controversy in chronic inflammatory demyelinating polyneuropathy.
PMID 12507413·Curr Neurol Neurosci Rep·2003
6-review
Peripheral Neuropathy Due to Cobalamin Deficiency.
PMID 11931726·Curr Treat Options Neurol·2002
8-other
Clinical spectrum of chronic acquired demyelinating polyneuropathies.
PMID 11353415·Muscle Nerve·2001
6-review
Motor neuron presentation of an ulnar neuropathy and Riche-Cannieu anastomosis.
PMID 10746189·Electromyogr Clin Neurophysiol·2000
5-case
Effects of long-term administration of 9-cis-retinyl acetate on visual function in mice.
PMID 18708622·Invest Ophthalmol Vis Sci·2009
7-preclinical
Phenotypic variability due to a novel Glu292Lys variation in exon 8 of the BEST1 gene causing best macular dystrophy.
PMID 19597114·Arch Ophthalmol·2009
8-other
A novel, efficient, randomized selection trial comparing combinations of drug therapy for ALS.
PMID 18608093·Amyotroph Lateral Scler·2008
3-trial
Impact of retinal disease-associated RPE65 mutations on retinoid isomerization.
PMID 18722466·Biochemistry·2008
7-preclinical
Combination treatment with reduced-fluence photodynamic therapy and intravitreal injection of triamcinolone for subfoveal choroidal neovascularization in macular degeneration.
PMID 18536593·Retina·2008
8-other
Novel RDH12 mutations associated with Leber congenital amaurosis and cone-rod dystrophy: biochemical and clinical evaluations.
PMID 17512964·Vision Res·2007
8-other
Adenoviral vector-delivered pigment epithelium-derived factor for neovascular age-related macular degeneration: results of a phase I clinical trial.
PMID 16454650·Hum Gene Ther·2006
3-trial
Autosomal recessive retinitis pigmentosa and E150K mutation in the opsin gene.
PMID 16737970·J Biol Chem·2006
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
- 9961 SIERRA AVE
FONTANA, CA 92335 - Phone
- (909) 427-3910
Quick Facts
- NPI
- 1992876973
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 58
- Publications
- 20
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