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DAVID SHARON, MD
MD
Hematology & Oncology Physician
NPI: 1730299041Individual
Specialties, Licenses & Credentials
Hematology & Oncology PhysicianPrimary
Internal Medicine — Hematology & Oncology
Code: 207RH0003X
25MA04046800(NJ)
Research & Publications (20)
Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice.
PMID 19409519·Am J Hum Genet·2009
7-preclinical
Naming a phantom - the quest to find the identity of Ulluchu, an unidentified ceremonial plant of the Moche culture in Northern Peru.
PMID 19335907·J Ethnobiol Ethnomed·2009
8-other
The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients.
PMID 19273793·Arch Ophthalmol·2009
8-other
Shadows of the colonial past--diverging plant use in Northern Peru and Southern Ecuador.
PMID 19187546·J Ethnobiol Ethnomed·2009
8-other
Lenalidomide and rituximab in Waldenstrom's macroglobulinemia.
PMID 19118065·Clin Cancer Res·2009
3-trial
Mapping the signal-to-noise-ratios of cortical sources in magnetoencephalography and electroencephalography.
PMID 18465745·Hum Brain Mapp·2009
8-other
Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi Jews.
PMID 18452394·Genet Test·2008
7-preclinical
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia.
PMID 18334930·Mol Vis·2008
8-other
Microarray-based gene expression analysis during retinal maturation of albino rats.
PMID 18286297·Graefes Arch Clin Exp Ophthalmol·2008
7-preclinical
Health for sale: the medicinal plant markets in Trujillo and Chiclayo, Northern Peru.
PMID 18070350·J Ethnobiol Ethnomed·2007
8-other
A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.
PMID 18055789·Invest Ophthalmol Vis Sci·2007
8-other
Toddler-parent psychotherapy increases secure attachment between toddlers and mothers who have experienced major depressive disorder.
PMID 17962683·Evid Based Ment Health·2007
8-other
Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like disease.
PMID 17724221·Invest Ophthalmol Vis Sci·2007
8-other
Multicenter clinical trial of bortezomib in relapsed/refractory Waldenstrom's macroglobulinemia: results of WMCTG Trial 03-248.
PMID 17545538·Clin Cancer Res·2007
3-trial
The advantage of combining MEG and EEG: comparison to fMRI in focally stimulated visual cortex.
PMID 17532230·Neuroimage·2007
4-observational
A complex expression pattern of Pax6 in the pigeon retina.
PMID 17525177·Invest Ophthalmol Vis Sci·2007
7-preclinical
A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa.
PMID 17480003·Am J Med Genet A·2007
8-other
Novel USH2A mutations in Israeli patients with retinitis pigmentosa and Usher syndrome type 2.
PMID 17296898·Arch Ophthalmol·2007
8-other
Traditional medicinal plant use in Northern Peru: tracking two thousand years of healing culture.
PMID 17090303·J Ethnobiol Ethnomed·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
- 100 STATE ROUTE 36, SUITE 1B
WEST LONG BRANCH, NJ 07764 - Phone
- (732) 222-1711
Quick Facts
- NPI
- 1730299041
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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