Hadas Newman

Chiasmal cavernoma: a rare cause of acute visual loss improved by prompt surgery.

Nonarteritic anterior ischemic optic neuropathy in a patient with primary acute angle-closure glaucoma.

Intraocular pressure changes in the contralateral eye after topical treatment: does an "ophthalmotonic consensual reaction" exist?

Systemic bevacizumab (Avastin) for exudative retinal detachment secondary to choroidal melanoma.

Subfoveal choroidal melanoma: pretreatment characteristics and response to plaque radiation therapy.

Involvement of CD24 in angiogenesis in a mouse model of oxygen-induced retinopathy.

The prevalence of retinal and optical coherence tomography findings in preeclamptic women.

Visually evoked potentials in a patient with a fyodorov-zuev keratoprosthesis.

Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT).

An intronic deletion in the PROM1 gene leads to autosomal recessive cone-rod dystrophy.

Partial thickness corneal tissue as a patch graft material for prevention of glaucoma drainage device exposure.

Optical Coherence Tomography: An Adjunctive Tool for Differentiating between Choroidal Melanoma and Metastasis.

Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.

Homozygosity for a Recessive Loss-of-Function Mutation of the NRL Gene Is Associated With a Variant of Enhanced S-Cone Syndrome.

Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.

Purification and characterization of human dehydrodolychil diphosphate synthase (DHDDS) overexpressed in E. coli.

Oculopharyngeal Muscular Dystrophy and Inherited Retinal Dystrophy in Bukhara Jews Due to Linked Mutations in the PABPN1 and NRL Genes.