Back to Search
CAMILLE BOON, M.D.
M.D.
Obstetrics & Gynecology Physician
NPI: 1932377512IndividualAccepts Medicare
Specialties, Licenses & Credentials
Obstetrics & Gynecology PhysicianPrimary
Obstetrics & Gynecology
Code: 207V00000X
M8545(TX)
CMS Specialties
PrimaryOBSTETRICS/GYNECOLOGY
Education
BAYLOR COLLEGE OF MEDICINE
Class of 2004
Research & Publications (20)
Clinical and molecular genetic analysis of best vitelliform macular dystrophy.
PMID 19357557·Retina·2009
8-other
The spectrum of phenotypes caused by variants in the CFH gene.
PMID 19297022·Mol Immunol·2009
6-review
Role of iron and hydroperoxides in the degradation of lycopene in oil-in-water emulsions.
PMID 19265448·J Agric Food Chem·2009
8-other
Co-regulation of Xanthomonas campestris virulence by quorum sensing and a novel two-component regulatory system RavS/RavR.
PMID 19220743·Mol Microbiol·2009
8-other
Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entity.
PMID 19540988·Am J Ophthalmol·2009
8-other
The spectrum of ocular phenotypes caused by mutations in the BEST1 gene.
PMID 19375515·Prog Retin Eye Res·2009
6-review
Near-infrared reflectance imaging of neovascular age-related macular degeneration.
PMID 19641931·Graefes Arch Clin Exp Ophthalmol·2009
4-observational
Factors affecting lycopene oxidation in oil-in-water emulsions.
PMID 18237137·J Agric Food Chem·2008
8-other
A novel DSF-like signal from Burkholderia cenocepacia interferes with Candida albicans morphological transition.
PMID 18049456·ISME J·2008
8-other
Half-molar sodium-lactate solution has a beneficial effect in patients after coronary artery bypass grafting.
PMID 18563389·Intensive Care Med·2008
2-rct
Recombinase-based reporter system and antisense technology to study gene expression and essentiality in hypoxic nonreplicating mycobacteria.
PMID 18544099·FEMS Microbiol Lett·2008
8-other
[Fundus autofluorescence in patients with inherited retinal diseases : patterns of fluorescence at two different wavelengths].
PMID 18415102·Ophthalmologe·2008
4-observational
The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene.
PMID 18328765·Prog Retin Eye Res·2008
6-review
Basal laminar drusen caused by compound heterozygous variants in the CFH gene.
PMID 18252232·Am J Hum Genet·2008
4-observational
Clinical and genetic heterogeneity in multifocal vitelliform dystrophy.
PMID 17698758·Arch Ophthalmol·2007
8-other
Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus.
PMID 17504850·Br J Ophthalmol·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
- 929 GESSNER RD, SUITE 2150
HOUSTON, TX 77024 - Phone
- (713) 935-9791
Quick Facts
- NPI
- 1932377512
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 22
- Publications
- 20
Are you this provider?
Claim Your Profile