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Robert K Koenekoop

Showing results (51-60 of 122) with videos related to

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JAMA Ophthalmology|February 16, 2013
Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290J Jason McAnany, Mohamed A Genead, Saloni Walia, et al.
European Child & Adolescent Psychiatry|August 3, 2014
Correlates, stability and predictors of borderline personality disorder among previously suicidal youthBrian Greenfield, Melissa Henry, Eric Lis, et al.
Molecular Vision|April 28, 2021
Noncoding mutation in <i>RPGRIP1</i> contributes to inherited retinal degenerationsGang Zou, Tao Zhang, Xuesen Cheng, et al.
Human Molecular Genetics|February 25, 2016
Mutations in POMGNT1 cause non-syndromic retinitis pigmentosaMingchu Xu, Takeyuki Yamada, Zixi Sun, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosisSuzanne Yzer, Gerald A Fishman, Julie Racine, et al.
Pharmacogenetics and Genomics|October 2, 2015
A genetic variant in NRP1 is associated with worse response to ranibizumab treatment in neovascular age-related macular degenerationLaura Lorés-Motta, Freekje van Asten, Philipp S Muether, et al.
Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Journal of Medical Genetics|April 17, 2014
A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular colobomaMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Lancet (London, England)|July 18, 2014
Oral 9-cis retinoid for childhood blindness due to Leber congenital amaurosis caused by RPE65 or LRAT mutations: an open-label phase 1b trialRobert K Koenekoop, Ruifang Sui, Juliana Sallum, et al.
Investigative Ophthalmology & Visual Science|May 11, 2013
Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosaQing Fu, Feng Wang, Hui Wang, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
JAMA Ophthalmology|February 16, 2013
Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290J Jason McAnany, Mohamed A Genead, Saloni Walia, et al.
European Child & Adolescent Psychiatry|August 3, 2014
Correlates, stability and predictors of borderline personality disorder among previously suicidal youthBrian Greenfield, Melissa Henry, Eric Lis, et al.
Molecular Vision|April 28, 2021
Noncoding mutation in <i>RPGRIP1</i> contributes to inherited retinal degenerationsGang Zou, Tao Zhang, Xuesen Cheng, et al.
Human Molecular Genetics|February 25, 2016
Mutations in POMGNT1 cause non-syndromic retinitis pigmentosaMingchu Xu, Takeyuki Yamada, Zixi Sun, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
CRB1 heterozygotes with regional retinal dysfunction: implications for genetic testing of leber congenital amaurosisSuzanne Yzer, Gerald A Fishman, Julie Racine, et al.
Pharmacogenetics and Genomics|October 2, 2015
A genetic variant in NRP1 is associated with worse response to ranibizumab treatment in neovascular age-related macular degenerationLaura Lorés-Motta, Freekje van Asten, Philipp S Muether, et al.
Ophthalmology|January 19, 2010
Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosaSaloni Walia, Gerald A Fishman, Samuel G Jacobson, et al.
Journal of Medical Genetics|April 17, 2014
A missense mutation in the splicing factor gene DHX38 is associated with early-onset retinitis pigmentosa with macular colobomaMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Lancet (London, England)|July 18, 2014
Oral 9-cis retinoid for childhood blindness due to Leber congenital amaurosis caused by RPE65 or LRAT mutations: an open-label phase 1b trialRobert K Koenekoop, Ruifang Sui, Juliana Sallum, et al.
Investigative Ophthalmology & Visual Science|May 11, 2013
Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosaQing Fu, Feng Wang, Hui Wang, et al.
Pageof 13