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DEBRA SHARON, PH.D.
PH.D.
Clinical Psychologist
NPI: 1104950286Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
PSY 8908(CA)
Research & Publications (20)
The advantage of combining MEG and EEG: comparison to fMRI in focally stimulated visual cortex.
PMID 17532230·Neuroimage·2007
4-observational
Shared mutations in NR2E3 in enhanced S-cone syndrome, Goldmann-Favre syndrome, and many cases of clumped pigmentary retinal degeneration.
PMID 12963616·Arch Ophthalmol·2003
8-other
RP2 and RPGR mutations and clinical correlations in patients with X-linked retinitis pigmentosa.
PMID 14564670·Am J Hum Genet·2003
8-other
Profile of the genes expressed in the human peripheral retina, macula, and retinal pigment epithelium determined through serial analysis of gene expression (SAGE).
PMID 11756676·Proc Natl Acad Sci U S A·2002
4-observational
Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases.
PMID 12037007·Invest Ophthalmol Vis Sci·2002
4-observational
Patients' violence towards the staff in psychiatric institutions--a professional and ethical dilemma.
PMID 11289642·Med Law·2000
8-other
X-linked retinitis pigmentosa: mutation spectrum of the RPGR and RP2 genes and correlation with visual function.
PMID 10937588·Invest Ophthalmol Vis Sci·2000
8-other
The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients.
PMID 19273793·Arch Ophthalmol·2009
8-other
Mapping the signal-to-noise-ratios of cortical sources in magnetoencephalography and electroencephalography.
PMID 18465745·Hum Brain Mapp·2009
8-other
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
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
Lenalidomide and rituximab in Waldenstrom's macroglobulinemia.
PMID 19118065·Clin Cancer Res·2009
3-trial
Shadows of the colonial past--diverging plant use in Northern Peru and Southern Ecuador.
PMID 19187546·J Ethnobiol Ethnomed·2009
8-other
Microarray-based gene expression analysis during retinal maturation of albino rats.
PMID 18286297·Graefes Arch Clin Exp Ophthalmol·2008
7-preclinical
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia.
PMID 18334930·Mol Vis·2008
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 complex expression pattern of Pax6 in the pigeon retina.
PMID 17525177·Invest Ophthalmol Vis Sci·2007
7-preclinical
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
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
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
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 6455 COLDWATER CANYON AVE
NORTH HOLLYWOOD, CA 91606 - Phone
- (818) 623-6340
Quick Facts
- NPI
- 1104950286
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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