Hasil Pencarian - Samer Khateb

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  1. 1
    Postoperative Macular Proliferative Vitreoretinopathy: A Case Series and Literature Review

    Postoperative Macular Proliferative Vitreoretinopathy: A Case Series and Literature Review oleh Samer Khateb, Hamzah Aweidah, Michael Halpert, Tareq Jaouni

    Diterbitkan 2021-05-01
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  2. 2
    Disease quiescence in endophthalmitis patients treated with anti-VEGF injections for retinal pathologies

    Disease quiescence in endophthalmitis patients treated with anti-VEGF injections for retinal pathologies oleh Brice Nguedia Vofo, Majd Saada, Antonio Rivera, Sigalit Cohen, Tareq Jaouni, Samer Khateb

    Diterbitkan 2024-02-01
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  3. 3
    Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Termination Codon in <i>FAM161A</i>

    Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Terminat... oleh Avigail Beryozkin, Ananya Samanta, Prakadeeswari Gopalakrishnan, Samer Khateb, Eyal Banin, Dror Sharon, Kerstin Nagel-Wolfrum

    Diterbitkan 2022-03-01
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  4. 4
    Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss.

    Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss. oleh Samer Khateb, Lina Zelinger, Tamar Ben-Yosef, Saul Merin, Ornit Crystal-Shalit, Menachem Gross, Eyal Banin, Dror Sharon

    Diterbitkan 2012-01-01
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  5. 5
    Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype–Phenotype Correlation in 228 Patients

    Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype–Phenotype Correlation in 228 Patients oleh Avigail Beryozkin, Hamzah Aweidah, Roque Daniel Carrero Valenzuela, Myriam Berman, Oscar Iguzquiza, Frans P. M. Cremers, Muhammad Imran Khan, Anand Swaroop, Radgonde Amer, Samer Khateb, Tamar Ben-Yosef, Dror Sharon, Eyal Banin

    Diterbitkan 2021-10-01
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  6. 6
    Genome wide association study and genomic risk prediction of age related macular degeneration in Israel

    Genome wide association study and genomic risk prediction of age related macular degeneration in Israel oleh Michelle Grunin, Daria Triffon, Gala Beykin, Elior Rahmani, Regev Schweiger, Liran Tiosano, Samer Khateb, Shira Hagbi-Levi, Batya Rinsky, Refael Munitz, Thomas W. Winkler, Iris M. Heid, Eran Halperin, Shai Carmi, Itay Chowers

    Diterbitkan 2024-06-01
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