Back to Search
MARTIN ABITBOL, M.D.
M.D.
Pediatrics Physician
NPI: 1356532162Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
ME107178(FL)
Research & Publications (20)
CX3CR1+ CD115+ CD135+ common macrophage/DC precursors and the role of CX3CR1 in their response to inflammation.
PMID 19273628·J Exp Med·2009
7-preclinical
Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes.
PMID 19129173·Hum Mol Genet·2009
7-preclinical
Morphologic and electroretinographic phenotype of SR-BI knockout mice after a long-term atherogenic diet.
PMID 19420333·Invest Ophthalmol Vis Sci·2009
7-preclinical
Expression of 8-oxoguanine DNA glycosylase (Ogg1) in mouse retina.
PMID 19503746·Mol Vis·2009
7-preclinical
Sirt1 involvement in rd10 mouse retinal degeneration.
PMID 19407027·Invest Ophthalmol Vis Sci·2009
7-preclinical
Analysis of partner of inscuteable (mPins) expression in the developing mouse eye.
PMID 19122831·Mol Vis·2008
7-preclinical
Reduction of brain metastases in plasminogen activator inhibitor-1-deficient mice with transgenic ocular tumors.
PMID 18753414·Carcinogenesis·2008
7-preclinical
ETS-1 and ETS-2 are upregulated in a transgenic mouse model of pigmented ocular neoplasm.
PMID 18958307·Mol Vis·2008
7-preclinical
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndrome.
PMID 18423520·Am J Hum Genet·2008
7-preclinical
Differential regulation of Dlg1, Scrib, and Lgl1 expression in a transgenic mouse model of ocular cancer.
PMID 19098995·Mol Vis·2008
7-preclinical
The RNA-binding protein Musashi-1 is produced in the developing and adult mouse eye.
PMID 17768378·Mol Vis·2007
7-preclinical
Novel human pathological mutations. Gene symbol: FZD4. Disease: familial exudative vitreoretinopathy.
PMID 17879448·Hum Genet·2007
8-other
A large genomic deletion in the PDHX gene caused by the retrotranspositional insertion of a full-length LINE-1 element.
PMID 17152059·Hum Mutat·2007
8-other
New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy.
PMID 17287362·J Med Genet·2007
8-other
Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
PMID 17417613·Mol Vis·2007
8-other
A gene transfer comparative study of HSA-conjugated antiangiogenic factors in a transgenic mouse model of metastatic ocular cancer.
PMID 17082795·Cancer Gene Ther·2007
7-preclinical
Increased plasma transferrin, altered body iron distribution, and microcytic hypochromic anemia in ferrochelatase-deficient mice.
PMID 17003376·Blood·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 9981 S HEALTHPARK DR
FORT MYERS, FL 33908 - Phone
- (239) 343-5651
Quick Facts
- NPI
- 1356532162
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile