Karen Hendler

Jerusalem, JM, Israel

Last Updated: 09/26/2026

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Found 27 publications

ANTI-VEGF THERAPY SWITCHING RETINAL DISEASES: Characterizing Clinical Manifestations and Common Involved Genes: ERRATUM.

ANTI-VEGF THERAPY SWITCHING RETINAL DISEASES: Characterizing Clinical Manifestations and Common Involved Genes: ERRATUM.

Journal: Retina (Philadelphia, Pa.)

Published: June 25, 2026

EARLY ONSET INHERITED RETINAL DISEASES Characterizing Clinical Manifestations and Common Involved Genes: Erratum.

EARLY ONSET INHERITED RETINAL DISEASES Characterizing Clinical Manifestations and Common Involved Genes: Erratum.

Journal: Retina (Philadelphia, Pa.)

Published: June 25, 2026

Early Onset Inherited Retinal Diseases: Characterizing Clinical Manifestations and Common Involved Genes.

Early Onset Inherited Retinal Diseases: Characterizing Clinical Manifestations and Common Involved Genes.

Journal: Retina (Philadelphia, Pa.)

Published: January 06, 2026

ANTI-VEGF THERAPY SWITCHING RETINAL DISEASES: Characterizing Clinical Manifestations and Common Involved Genes.

ANTI-VEGF THERAPY SWITCHING RETINAL DISEASES: Characterizing Clinical Manifestations and Common Involved Genes.

Journal: Retina (Philadelphia, Pa.)

Published: January 06, 2026

Exploring the role of low-dose atropine in myopia management in children with inherited retinal diseases.

Exploring the role of low-dose atropine in myopia management in children with inherited retinal diseases.

Journal: Optometry and vision science : official publication of the American Academy of Optometry

Published: December 25, 2025

Natural course of refractive errors in early onset inherited retinal diseases.

Natural course of refractive errors in early onset inherited retinal diseases.

Journal: Eye (London, England)

Published: March 06, 2025

The importance of genetic counselling and testing in inherited eye diseases: A population-based retrospective study.

The importance of genetic counselling and testing in inherited eye diseases: A population-based retrospective study.

Journal: PloS one

Published: June 16, 2024

Nystagmus in infancy: causes, characteristics and main tools for diagnosis.

Nystagmus in infancy: causes, characteristics and main tools for diagnosis.

Journal: Eye (London, England)

Published: June 09, 2024

Genetics of bilateral pediatric cataract in the Israeli and Palestinian populations.

Genetics of bilateral pediatric cataract in the Israeli and Palestinian populations.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: February 15, 2024

The prevalence of autism among children with albinism.

The prevalence of autism among children with albinism.

Journal: European journal of ophthalmology

Published: October 03, 2023

Visual acuity improvement in children with albinism beyond the first decade of life.

Visual acuity improvement in children with albinism beyond the first decade of life.

Journal: PloS one

Published: July 30, 2023

Whole exome sequencing of 491 individuals with inherited retinal diseases reveals a large spectrum of variants and identification of novel candidate genes.

Whole exome sequencing of 491 individuals with inherited retinal diseases reveals a large spectrum of variants and identification of novel candidate genes.

Journal: Journal of medical genetics

Published: June 27, 2023

Showing 1-12 of 27

Last Updated: 09/26/2026