Lista de obras -

An Ashkenazi Jewish founder mutation in CACNA1F causes retinal phenotype in both hemizygous males and heterozygous female carriers

scientific article published on 25 October 2019

Bilateral iridociliary T-cell lymphoma.

artículo científico publicado en 2002

Botulinum toxin in the treatment of strabismus. A review of its use and effects

artículo científico publicado en 2007

Chiari 1 malformation presenting as strabismus.

artículo científico publicado en 2006

Combined Occurrence of Autosomal Dominant Aniridia and Autosomal Recessive Albinism in Several Members of a Family

artículo científico publicado en 2015

Does postmenopausal hormone replacement therapy affect intraocular pressure?

artículo científico publicado en 2005

Expression and activation of toll-like receptor 3 and toll-like receptor 4 on human corneal epithelial and conjunctival fibroblasts.

artículo científico publicado en 2014

Forty years of changing indications in penetrating keratoplasty in Israel

artículo científico publicado en 2005

Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism

artículo científico publicado en 2021

Graded Anderson procedure for correcting abnormal head posture in infantile nystagmus

scientific article published on 25 March 2019

Injury induced by chemical warfare agents: characterization and treatment of ocular tissues exposed to nitrogen mustard.

artículo científico publicado en 2003

Lateral orbitotomy in the management of challenging exotropia

scientific article published on July 2009

Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease

scientific article published on 30 August 2018

Nitric oxide secretion in human conjunctival fibroblasts is inhibited by alpha linolenic acid.

artículo científico publicado en 2015

Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease

artículo científico publicado en 2018

Prevalence and factors related to visual impairments in children with bilateral cataract following surgery and the potential need for education and rehabilitation services

artículo científico publicado en 2022

Prevalence of Strabismus Among Children With Neurofibromatosis Type 1 Disease With and Without Optic Pathway Glioma

artículo científico publicado en 2018

Progressive Visual Loss Without Retinal Detachment in Stickler Syndrome: An Uncommon and Novel Presentation

scientific article published on 01 December 2020

Red-Tinted Contact Lenses May Improve Quality of Life in Retinal Diseases.

artículo científico publicado en 2015

Refractive profile in oculocutaneous albinism and its correlation with final visual outcome

scientific article published on 01 December 2011

Strabismus surgery outcome among children and young adults with Down syndrome

artículo científico publicado en 2010

TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations

scientific article published on 19 August 2019

The effect of hormone therapy on the risk for age-related maculopathy in postmenopausal women

artículo científico publicado en 2004

The learning effect in visual field testing of healthy subjects using frequency doubling technology

artículo científico publicado en 2002

Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children

artículo científico publicado en 2020

When pediatric acute acquired comitant esotropia is not caused by a neurological disease

artículo científico publicado en 2020

Lista de obras de

An Ashkenazi Jewish founder mutation in CACNA1F causes retinal phenotype in both hemizygous males and heterozygous female carriers

Bilateral iridociliary T-cell lymphoma.

Botulinum toxin in the treatment of strabismus. A review of its use and effects

Chiari 1 malformation presenting as strabismus.

Combined Occurrence of Autosomal Dominant Aniridia and Autosomal Recessive Albinism in Several Members of a Family

Does postmenopausal hormone replacement therapy affect intraocular pressure?

Expression and activation of toll-like receptor 3 and toll-like receptor 4 on human corneal epithelial and conjunctival fibroblasts.

Forty years of changing indications in penetrating keratoplasty in Israel

Genetic causes of nystagmus, foveal hypoplasia and subnormal visual acuity- other than albinism

Graded Anderson procedure for correcting abnormal head posture in infantile nystagmus

Injury induced by chemical warfare agents: characterization and treatment of ocular tissues exposed to nitrogen mustard.

Lateral orbitotomy in the management of challenging exotropia

Mild aniridia phenotype: an under-recognized diagnosis of a severe inherited ocular disease

Nitric oxide secretion in human conjunctival fibroblasts is inhibited by alpha linolenic acid.

Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease

Prevalence and factors related to visual impairments in children with bilateral cataract following surgery and the potential need for education and rehabilitation services

Prevalence of Strabismus Among Children With Neurofibromatosis Type 1 Disease With and Without Optic Pathway Glioma

Progressive Visual Loss Without Retinal Detachment in Stickler Syndrome: An Uncommon and Novel Presentation

Red-Tinted Contact Lenses May Improve Quality of Life in Retinal Diseases.

Refractive profile in oculocutaneous albinism and its correlation with final visual outcome

Strabismus surgery outcome among children and young adults with Down syndrome

TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations

The effect of hormone therapy on the risk for age-related maculopathy in postmenopausal women

The learning effect in visual field testing of healthy subjects using frequency doubling technology

Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children

When pediatric acute acquired comitant esotropia is not caused by a neurological disease