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Elise Heon

Showing results (11-20 of 87) with videos related to

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Pediatric Radiology|August 13, 2016
The role of MR imaging in investigating isolated pediatric nystagmusVaishnavi Batmanabane, Elise Heon, Tianyang Dai, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 13, 2003
Ocular motility changes after subtenon carboplatin chemotherapy for retinoblastomaAlan Mulvihill, Andrew Budning, Venita Jay, et al.
American Journal of Medical Genetics. Part A|July 26, 2017
Agenesis of the corpus callosum, developmental delay, autism spectrum disorder, facial dysmorphism, and posterior polymorphous corneal dystrophy associated with ZEB1 gene deletionAyeshah Chaudhry, Brian H Chung, Dimitri J Stavropoulos, et al.
Investigative Ophthalmology & Visual Science|January 24, 2013
Intervisit variability of visual parameters in Leber congenital amaurosis caused by RPE65 mutationsAlejandro J Roman, Artur V Cideciyan, Sharon B Schwartz, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastomaAngela Punnett, Ikuko Teshima, Elise Heon, et al.
Investigative Ophthalmology & Visual Science|December 4, 2025
Genetic Spectrum of Negative Electroretinograms in a Predominantly Pediatric Cohort of 177 PatientsKirill Zaslavsky, Anupreet Tumber, Eoghan Millar, et al.
Investigative Ophthalmology & Visual Science|September 13, 2018
Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 YearsArtur V Cideciyan, Jason Charng, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|July 14, 2016
Visual Function and Central Retinal Structure in ChoroideremiaElise Heon, Talal Alabduljalil, David B McGuigan III, et al.
Molecular Vision|June 1, 2006
Further support of the role of CYP1B1 in patients with Peters anomalyAndrea Vincent, Gail Billingsley, Megan Priston, et al.
The New England Journal of Medicine|May 5, 2015
Improvement and decline in vision with gene therapy in childhood blindnessSamuel G Jacobson, Artur V Cideciyan, Alejandro J Roman, et al.
Pageof 9

Showing results (11-20 of 87) with videos related to

Sort By:
Pageof 9
Pediatric Radiology|August 13, 2016
The role of MR imaging in investigating isolated pediatric nystagmusVaishnavi Batmanabane, Elise Heon, Tianyang Dai, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 13, 2003
Ocular motility changes after subtenon carboplatin chemotherapy for retinoblastomaAlan Mulvihill, Andrew Budning, Venita Jay, et al.
American Journal of Medical Genetics. Part A|July 26, 2017
Agenesis of the corpus callosum, developmental delay, autism spectrum disorder, facial dysmorphism, and posterior polymorphous corneal dystrophy associated with ZEB1 gene deletionAyeshah Chaudhry, Brian H Chung, Dimitri J Stavropoulos, et al.
Investigative Ophthalmology & Visual Science|January 24, 2013
Intervisit variability of visual parameters in Leber congenital amaurosis caused by RPE65 mutationsAlejandro J Roman, Artur V Cideciyan, Sharon B Schwartz, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastomaAngela Punnett, Ikuko Teshima, Elise Heon, et al.
Investigative Ophthalmology & Visual Science|December 4, 2025
Genetic Spectrum of Negative Electroretinograms in a Predominantly Pediatric Cohort of 177 PatientsKirill Zaslavsky, Anupreet Tumber, Eoghan Millar, et al.
Investigative Ophthalmology & Visual Science|September 13, 2018
Progression in X-linked Retinitis Pigmentosa Due to ORF15-RPGR Mutations: Assessment of Localized Vision Changes Over 2 YearsArtur V Cideciyan, Jason Charng, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|July 14, 2016
Visual Function and Central Retinal Structure in ChoroideremiaElise Heon, Talal Alabduljalil, David B McGuigan III, et al.
Molecular Vision|June 1, 2006
Further support of the role of CYP1B1 in patients with Peters anomalyAndrea Vincent, Gail Billingsley, Megan Priston, et al.
The New England Journal of Medicine|May 5, 2015
Improvement and decline in vision with gene therapy in childhood blindnessSamuel G Jacobson, Artur V Cideciyan, Alejandro J Roman, et al.
Pageof 9