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American Journal of Ophthalmology
|
April 5, 2002
Effective treatment of ligneous conjunctivitis with topical plasminogen
Patrick Watts, Palanisamy Suresh, Eedy Mezer, et al.
Ophthalmic Genetics
|
April 25, 2007
Attitudes regarding predictive testing for retinitis pigmentosa
Eedy Mezer, Riyana Babul-Hirji, Richard Wise, et al.
Investigative Ophthalmology & Visual Science
|
May 26, 2007
Screening and diagnosis of optic pathway gliomas in children with neurofibromatosis type 1 by using sweep visual evoked potentials
Benjamin C M Chang, Giuseppe Mirabella, Ronit Yagev, et al.
European Journal of Ophthalmology
|
May 28, 2025
Wait times in pediatric ophthalmology clinics: Insights from a tertiary university hospital
Achia Nemet, Asaf Israeli, Tzadok Yona, et al.
Molecular Vision
|
January 6, 2012
Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1
Leah Rizel, Christine Safieh, Stavit A Shalev, et al.
International Ophthalmology
|
July 6, 2023
Is there room for prompt routine ophthalmic examination in neonates with congenital cytomegalovirus (CMV) infection during the neonatal period?
Michael Mimouni, Liron Naftali Ben-Haim, Efrat Naaman, et al.
International Ophthalmology
|
October 14, 2024
An international survey on retinopathy of prematurity practice patterns during the COVID-19 pandemic and lessons for future management
Rachel Shemesh, Michael Chiang, R V Paul Chan, et al.
Archives of Disease in Childhood
|
May 2, 2013
Oral propranolol versus placebo for retinopathy of prematurity: a pilot, randomised, double-blind prospective study
Imad R Makhoul, Ofra Peleg, Benjamin Miller, et al.
Molecular Vision
|
March 2, 2019
A novel intronic mutation of <i>PDE6B</i> is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews
Yasmin Tatour, Jonathan Tamaiev, Shamaly Shamaly, et al.
Scientific Reports
|
September 17, 2020
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations
Avigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 67) with videos related to
Sort By:
Page
of 7
American Journal of Ophthalmology
|
April 5, 2002
Effective treatment of ligneous conjunctivitis with topical plasminogen
Patrick Watts, Palanisamy Suresh, Eedy Mezer, et al.
Ophthalmic Genetics
|
April 25, 2007
Attitudes regarding predictive testing for retinitis pigmentosa
Eedy Mezer, Riyana Babul-Hirji, Richard Wise, et al.
Investigative Ophthalmology & Visual Science
|
May 26, 2007
Screening and diagnosis of optic pathway gliomas in children with neurofibromatosis type 1 by using sweep visual evoked potentials
Benjamin C M Chang, Giuseppe Mirabella, Ronit Yagev, et al.
European Journal of Ophthalmology
|
May 28, 2025
Wait times in pediatric ophthalmology clinics: Insights from a tertiary university hospital
Achia Nemet, Asaf Israeli, Tzadok Yona, et al.
Molecular Vision
|
January 6, 2012
Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1
Leah Rizel, Christine Safieh, Stavit A Shalev, et al.
International Ophthalmology
|
July 6, 2023
Is there room for prompt routine ophthalmic examination in neonates with congenital cytomegalovirus (CMV) infection during the neonatal period?
Michael Mimouni, Liron Naftali Ben-Haim, Efrat Naaman, et al.
International Ophthalmology
|
October 14, 2024
An international survey on retinopathy of prematurity practice patterns during the COVID-19 pandemic and lessons for future management
Rachel Shemesh, Michael Chiang, R V Paul Chan, et al.
Archives of Disease in Childhood
|
May 2, 2013
Oral propranolol versus placebo for retinopathy of prematurity: a pilot, randomised, double-blind prospective study
Imad R Makhoul, Ofra Peleg, Benjamin Miller, et al.
Molecular Vision
|
March 2, 2019
A novel intronic mutation of <i>PDE6B</i> is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews
Yasmin Tatour, Jonathan Tamaiev, Shamaly Shamaly, et al.
Scientific Reports
|
September 17, 2020
Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations
Avigail Beryozkin, Samer Khateb, Carlos Alberto Idrobo-Robalino, et al.
Page
of 7