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ANTHONY ALDAVE, MD

MD

Ophthalmology Physician

NPI: 1316050578IndividualAccepts Medicare

Specialties, Licenses & Credentials

Ophthalmology PhysicianPrimary

Ophthalmology

Code: 207W00000X

A71201(CA)

CMS Specialties

PrimaryOPHTHALMOLOGY

Education

UNIVERSITY OF TEXAS MEDICAL BRANCH AT GALVESTON

Class of 1996

Research & Publications (20)

Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval.
PMID 19574904·Cornea·2009
8-other
The Boston type I keratoprosthesis: improving outcomes and expanding indications.
PMID 19243830·Ophthalmology·2009
8-other
A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.
PMID 18332318·Arch Ophthalmol·2008
5-case
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.
PMID 17935237·Am J Med Genet A·2007
8-other
Keratoconus is not associated with mutations in COL8A1 and COL8A2.
PMID 17721297·Cornea·2007
8-other
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.
PMID 17667634·Cornea·2007
5-case
Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.
PMID 17558846·Ophthalmic Genet·2007
8-other
A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy.
PMID 17317389·Am J Ophthalmol·2007
5-case
Elucidating the molecular genetic basis of the corneal dystrophies: are we there yet?
PMID 17296893·Arch Ophthalmol·2007
6-review
No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy.
PMID 16936088·Invest Ophthalmol Vis Sci·2006
8-other
Corneal copper deposition associated with chronic lymphocytic leukemia.
PMID 16815276·Am J Ophthalmol·2006
5-case
No VSX1 gene mutations associated with keratoconus.
PMID 16799019·Invest Ophthalmol Vis Sci·2006
8-other
No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition.
PMID 16670477·Cornea·2006
5-case
Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene.
PMID 16541014·Mol Vis·2006
5-case
Analysis of fifteen positional candidate genes for Schnyder crystalline corneal dystrophy.
PMID 16163269·Mol Vis·2005
8-other
A unique corneal dystrophy of Bowman's layer and stroma associated with the Gly623Asp mutation in the transforming growth factor beta-induced (TGFBI) gene.
PMID 15885785·Ophthalmology·2005
5-case
Candidate gene screening for posterior polymorphous dystrophy.
PMID 15725882·Cornea·2005
8-other
Lattice dystrophy-like localized amyloidosis of the cornea secondary to trichiasis.
PMID 15604878·Cornea·2005
5-case
Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.
PMID 15531312·Am J Ophthalmol·2004
5-case
Anterior basement membrane corneal dystrophy and pseudo-unilateral lattice corneal dystrophy in a patient with recurrent corneal erosions.
PMID 15183802·Am J Ophthalmol·2004
5-case

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Via practice · 2 locations total

Address
100 STEIN PLAZA
LOS ANGELES, CA 90095

Locations (2)

Practice Location

100 STEIN PLAZA, LOS ANGELES, CA
(310) 794-7770

Practice Location

200 STEIN PLAZA, LOS ANGELES, CA
(310) 206-7202

Quick Facts

NPI
1316050578
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
2
Years in Practice
30
Publications
20

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