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Hadas Newman

Showing results (21-30 of 37) with videos related to

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Retina (Philadelphia, Pa.)|September 21, 2022
ReplyHadas 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 AlbipunctatusHadas Newman, Ido Perlman, Eran Pras, et al.
Clinical Ophthalmology (Auckland, N.Z.)|March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophyDaniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
Ophthalmology|December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical AspectsAdva 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 mutationsAvigail 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 LossPrasanthi 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 LossPrasanthi 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 AssociationTamar 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 MechanismYogapriya Sundaresan, Antonio Rivera, Alexey Obolensky, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Retina (Philadelphia, Pa.)|September 21, 2022
ReplyHadas 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 AlbipunctatusHadas Newman, Ido Perlman, Eran Pras, et al.
Clinical Ophthalmology (Auckland, N.Z.)|March 19, 2019
Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophyDaniel Ben Ner, Ifat Sher, Amit Hamburg, et al.
Ophthalmology|December 26, 2017
Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical AspectsAdva 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 mutationsAvigail 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 LossPrasanthi 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 LossPrasanthi 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 AssociationTamar 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 MechanismYogapriya Sundaresan, Antonio Rivera, Alexey Obolensky, et al.
Pageof 4