Uveitis after the BNT162b2 mRNA vaccination against SARS-CoV-2 infection: a possible association

…, B Shaer, V Vishnevskia-Dai, S Shulman, H Newman… - Retina, 2021 - journals.lww.com
Purpose: To describe uveitis cases after the BNT162b2 mRNA SARS-CoV-2 vaccination.
Methods: This is a multicenter, retrospective study. Vaccine-related uveitis diagnosis was …

A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)

…, OS Birk, M Ehrenberg, R Leibu, H Newman… - Human …, 2020 - Wiley Online Library
Inherited retinal diseases (IRDs) cause visual loss due to dysfunction or progressive
degeneration of photoreceptors. These diseases show marked phenotypic and genetic …

Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics

…, MD Mena, I Meunier, R Miller, H Newman… - Genetics in …, 2020 - nature.com
Purpose Missing heritability in human diseases represents a major challenge, and this is
particularly true for ABCA4-associated Stargardt disease (STGD1). We aimed to elucidate the …

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

L Haer-Wigman, H Newman, R Leibu… - Human molecular …, 2015 - academic.oup.com
Retinitis pigmentosa (RP), the most common form of inherited retinal degeneration, is
clinically and genetically heterogeneous and can appear as syndromic or non-syndromic. …

[PDF][PDF] Bi-allelic truncating mutations in CEP78, encoding centrosomal protein 78, cause cone-rod degeneration with sensorineural hearing loss

…, E Pras, T Ben-Yosef, H Newman… - The American Journal of …, 2016 - cell.com
Inherited retinal diseases (IRDs) are a diverse group of genetically and clinically heterogeneous
retinal abnormalities. The present study was designed to identify genetic defects in …

Nonsyndromic retinitis pigmentosa in the Ashkenazi Jewish population: genetic and clinical aspects

…, E Pras, SG Jacobson, T Ben-Yosef, H Newman… - Ophthalmology, 2018 - Elsevier
Purpose To analyze the genetic and clinical findings in retinitis pigmentosa (RP) patients of
Ashkenazi Jewish (AJ) descent, aiming to identify genotype–phenotype correlations. Design …

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

M Neudorfer, O Spierer, M Goder, H Newman, S Barak… - Retina, 2014 - journals.lww.com
Purpose: To evaluate retinal and optical coherence tomography findings and establish their
prevalence in preeclamptic women. Methods: Twenty-seven preeclamptic women who …

Home use of binocular dichoptic video content device for treatment of amblyopia: a pilot study

D Mezad-Koursh, A Rosenblatt, H Newman… - Journal of American …, 2018 - Elsevier
Purpose To evaluate the efficacy of the BinoVision home system as measured by improvement
of visual acuity in the patient's amblyopic eye. Methods An open-label prospective pilot-…

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

O Spierer, M Waisbourd, Y Golan, H Newman… - BMC …, 2016 - Springer
Background To protect from erosion of the tube in glaucoma drainage device (GDD), the
tube is covered by a biologic tissue which is roofed by the conjunctiva. Sclera, pericardium, …

[HTML][HTML] Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry

…, FPM Cremers, E Pras, D Zur, H Newman… - Molecular …, 2023 - ncbi.nlm.nih.gov
Purpose This study sought to describe the phenotype frequency and genetic basis of inherited
retinal diseases (IRDs) among a nationwide cohort of Israeli Jewish patients of Ethiopian …