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Retina (Philadelphia, Pa.)
|
September 21, 2022
Reply
Hadas Newman, Ido Perlman, Eran Pras, et al.
Retina (Philadelphia, Pa.)
|
March 7, 2022
THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus
Hadas Newman, Ido Perlman, Eran Pras, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy
Daniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
Ophthalmology
|
December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects
Adva Kimchi, Samer Khateb, Rong Wen, 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.
American Journal of Human Genetics
|
November 5, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss
Prasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
American Journal of Human Genetics
|
September 3, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss
Prasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
Retina (Philadelphia, Pa.)
|
August 9, 2021
UVEITIS AFTER THE BNT162b2 mRNA VACCINATION AGAINST SARS-CoV-2 INFECTION: A Possible Association
Tamar Rabinovitch, Yael Ben-Arie-Weintrob, Tamar Hareuveni-Blum, et al.
Harefuah
|
February 20, 2019
[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES]
Dror Sharon, Tamar Ben-Yosef, Eran Pras, et al.
Genes
|
June 27, 2024
Genetic and Clinical Analyses of the <i>KIZ</i>-c.226C>T Variant Resulting in a Dual Mutational Mechanism
Yogapriya Sundaresan, Antonio Rivera, Alexey Obolensky, et al.
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Search research articles
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Showing results (21-30 of 37) with videos related to
Sort By:
Page
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Retina (Philadelphia, Pa.)
|
September 21, 2022
Reply
Hadas Newman, Ido Perlman, Eran Pras, et al.
Retina (Philadelphia, Pa.)
|
March 7, 2022
THE TARGET SIGN: A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5-Related Fundus Albipunctatus
Hadas Newman, Ido Perlman, Eran Pras, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy
Daniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
Ophthalmology
|
December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects
Adva Kimchi, Samer Khateb, Rong Wen, 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.
American Journal of Human Genetics
|
November 5, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss
Prasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
American Journal of Human Genetics
|
September 3, 2016
Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss
Prasanthi Namburi, Rinki Ratnapriya, Samer Khateb, et al.
Retina (Philadelphia, Pa.)
|
August 9, 2021
UVEITIS AFTER THE BNT162b2 mRNA VACCINATION AGAINST SARS-CoV-2 INFECTION: A Possible Association
Tamar Rabinovitch, Yael Ben-Arie-Weintrob, Tamar Hareuveni-Blum, et al.
Harefuah
|
February 20, 2019
[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES]
Dror Sharon, Tamar Ben-Yosef, Eran Pras, et al.
Genes
|
June 27, 2024
Genetic and Clinical Analyses of the <i>KIZ</i>-c.226C>T Variant Resulting in a Dual Mutational Mechanism
Yogapriya Sundaresan, Antonio Rivera, Alexey Obolensky, et al.
Page
of 4