Practice: Anthony J. Aldave, MD
Back to Jules Stein Eye Institute

 

 
100 Stein Plaza, UCLA
Los Angeles, CA 90095-7002
Phone: (310) 206-7202
Fax: (310) 794-7906

Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.
An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutation.
Keratoconus is not associated with mutations in COL8A1 and COL8A2.
Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.
Ocular surface toxicity associated with topical interferon alpha-2b.
Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.
Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20.
A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy.
Elucidating the molecular genetic basis of the corneal dystrophies: are we there yet?
Amniotic membrane transplantation with anterior stromal micropuncture for treatment of painful bullous keratopathy in eyes with poor visual potential.
No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy.
Corneal copper deposition associated with chronic lymphocytic leukemia.
No VSX1 gene mutations associated with keratoconus.
No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition.
Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene.
Analysis of fifteen positional candidate genes for Schnyder crystalline corneal dystrophy.
Late calcific deposition on the hydrophilic acrylic MemoryLens.
A unique corneal dystrophy of Bowman's layer and stroma associated with the Gly623Asp mutation in the transforming growth factor beta-infuced (TGFBI) gene.
Primary graft failure associated with epithelial downgrowth: a case report.
No pathogenic mutations identified in the COL8A2 gene or four positional candidate genes in patients with posterior polymorphous corneal dystrophy.
Management of prominent iris vascular tufts causing recurrent spontaneous hyphema.
Candidate gene screening for posterior polymorphous dystrophy.
VSX1 mutation and corneal dystrophies.
Epithelial downgrowth following surgery for congenital glaucoma.
Lattice dystrophy-like localized amyloidosis of the cornea secondary to trichiasis.
Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.
Drug-induced corneal complications.
Macular hemorrhage after laser in situ keratomileusis (LASIK) with femtosecond laser flap creation.
The usefulness of buccal swabs for mutation screening in patients with suspected corneal dystrophies.
Anterior basement membrane corneal dystrophy and pseudo-unilateral lattice corneal dystrophy in a patient with recurrent corneal erosions.
Novel mutations in the carbohydrate sulfotransferase gene (CHST6) in American patients with macular corneal dystrophy.
Novel mutations in the CHST6 gene associated with macular corneal dystrophy in southern India.
Atypical vortex pattern of corneal deposits in granular corneal dystrophy.
Spontaneous corneal hydrops and perforation in both eyes of a patient with pellucid marginal degeneration.
Histopathological analysis of the cornea after laser in situ keratomileusis.
Peripheral keratitis associated with erythema elevatum diutinum.
Spontaneous corneal hydrops and perforation in keratoconus and pellucid marginal degeneration.
A novel technique for harvesting keratolimbal allografts from corneoscleral buttons.
Central discoid corneal dystrophy.
Examination of affected relatives and molecular genetic analysis are best means to differentiate between early granular and combined granular-lattice corneal dystrophies.
Late-onset traumatic flap dislocation and diffuse lamellar inflammation after laser in situ keratomileusis.
Ocular bungee cord injuries.
Advances in the management of lower eyelid retraction.
Ocular syphilis.
The molecular genetics of Bowman's layer dystrophies.
Bungee cord-associated ocular trauma.
Congenital corneal opacification in De Barsy syndrome.
The role of glaucoma therapy in the need for repeat penetrating keratoplasty.
Treatment strategies for postoperative Propionibacterium acnes endophthalmitis.
Surgical excision of selected amblyogenic periorbital capillary hemangiomas.
Ocular manifestations of immunologic and rheumatologic inflammatory disorders.
The eye and the eosinophil.