Anat Blumenfeld

Recombinant Human Amelogenin Protein Enhances Tendon‐To‐Bone Healing in a Rat Rotator Cuff Tear Model

Amelogenin Null Mice Develop Osteoarthritis, While Its Application Mitigates Disease Phenotypes in a Rat Model

Best Disease: Global Mutations Review, Genotype–Phenotype Correlation, and Prevalence Analysis in the Israeli Population

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

Regeneration of injured articular cartilage using the recombinant human amelogenin protein

The prevalence of autism among children with albinism

The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism: Similarities and Differences

Childhood visual impairment and blindness: 5-year data from a tertiary low vision center in Israel

A deep intronic substitution in <i>CNGB3</i> is one of the major causes of achromatopsia among Jewish patients.

Regeneration of grade 3 ankle sprain, using the recombinant human amelogenin protein (rHAM⁺) in a rat model

Tuftelin Is Required for NGF-Induced Differentiation of PC12 Cells

Tuftelin's involvement in embryonic development

Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli population

Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population

Skeletal ligament healing using the recombinant human amelogenin protein

Retinitis pigmentosa caused by mutations in the ciliary <i><scp>MAK</scp></i> gene is relatively mild and is not associated with apparent extra‐ocular features