Visually Evoked Potentials in a Patient with a Fyodorov-Zuev Keratoprosthesis

por Schwartz, Roy, Barak, Adiel, Newman, Hadas
Publicado 2015

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

por Spierer, Oriel, Waisbourd, Michael, Golan, Yitzhak, Newman, Hadas, Rachmiel, Rony
Publicado 2016

An intronic deletion in the PROM1 gene leads to autosomal recessive cone-rod dystrophy

por Eidinger, Osnat, Leibu, Rina, Newman, Hadas, Rizel, Leah, Perlman, Ido, Ben-Yosef, Tamar
Publicado 2015

Optical Coherence Tomography: An Adjunctive Tool for Differentiating between Choroidal Melanoma and Metastasis

por Vishnevskia-Dai, Vicktoria, Zur, Dinah, Yaacobi, Shiran, Moroz, Iris, Newman, Hadas, Neudorfer, Meira
Publicado 2016

Structural Characterization of Full-Length Human Dehydrodolichyl Diphosphate Synthase Using an Integrative Computational and Experimental Approach

por Lisnyansky Bar-El, Michal, Lee, Su Youn, Ki, Ah Young, Kapelushnik, Noa, Loewenstein, Anat, Chung, Ka Young, Schneidman-Duhovny, Dina, Giladi, Moshe, Newman, Hadas, Haitin, Yoni
Publicado 2019

Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy

por Ben Ner, Daniel, Sher, Ifat, Hamburg, Amit, Mhajna, Mohamad O, Chibel, Ron, Derazne, Estela, Sharvit-Ginon, Inbal, Pras, Eran, Newman, Hadas, Levy, Jaime, Khateb, Samer, Sharon, Dror, Rotenstreich, Ygal
Publicado 2019

Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations

por Beryozkin, Avigail, Khateb, Samer, Idrobo-Robalino, Carlos Alberto, Khan, Muhammad Imran, Cremers, Frans P. M., Obolensky, Alexey, Hanany, Mor, Mezer, Eedy, Chowers, Itay, Newman, Hadas, Ben-Yosef, Tamar, Sharon, Dror, Banin, Eyal
Publicado 2020

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

por Haer-Wigman, Lonneke, Newman, Hadas, Leibu, Rina, Bax, Nathalie M., Baris, Hagit N, Rizel, Leah, Banin, Eyal, Massarweh, Amir, Roosing, Susanne, Lefeber, Dirk J., Zonneveld-Vrieling, Marijke N., Isakov, Ofer, Shomron, Noam, Sharon, Dror, Den Hollander, Anneke I., Hoyng, Carel B., Cremers, Frans P.M., Ben-Yosef, Tamar
Publicado 2015

Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry

por Ben Yosef, Tamar, Banin, Eyal, Chervinsky, Elana, Shalev, Stavit A., Leibu, Rina, Mezer, Eedy, Rotenstreich, Ygal, Goldenberg-Cohen, Nitza, Weiss, Shirel, Khan, Muhammad Imran, Panneman, Daan M., Hitti-Malin, Rebekkah J., Weiner, Chen, Roosing, Susanne, Cremers, Frans P. M., Pras, Eran, Zur, Dinah, Newman, Hadas, Deitch, Iris, Sharon, Dror, Ehrenberg, Miriam
Publicado 2023