Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Liliana Mizrahi-Meissonnier

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Investigative Ophthalmology & Visual Science|March 12, 2010
Variable retinal phenotypes caused by mutations in the X-linked photopigment gene arrayLiliana Mizrahi-Meissonnier, Saul Merin, Eyal Banin, et al.
American Journal of Ophthalmology|May 29, 2012
Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in DenmarkHanna Bitner, Patrik Schatz, Liliana Mizrahi-Meissonnier, et al.
Investigative Ophthalmology & Visual Science|April 7, 2011
A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive modeHanna Bitner, Liliana Mizrahi-Meissonnier, Gabriel Griefner, et al.
Prenatal Diagnosis|July 24, 2009
Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli familiesAda Rosenmann, Idit Bejarano-Achache, Dalia Eli, et al.
Molecular Vision|May 19, 2012
A tapetal-like fundus reflex in a healthy male: evidence against a role in the pathophysiology of retinal degeneration?Patrik Schatz, Jesper Bregnhøj, Henrik Arvidsson, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like diseaseAnat Beit-Ya'acov, Liliana Mizrahi-Meissonnier, Alexey Obolensky, et al.
Journal of Medical Genetics|May 1, 2014
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndromeSamer Khateb, Lina Zelinger, Liliana Mizrahi-Meissonnier, et al.
American Journal of Medical Genetics. Part A|May 8, 2007
A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosaEyal Banin, Liliana Mizrahi-Meissonnier, Ruhama Neis, et al.
American Journal of Ophthalmology|December 19, 2013
Ocular phenotype analysis of a family with biallelic mutations in the BEST1 geneDror Sharon, Sermed Al-Hamdani, Karl Engelsberg, et al.
Frontiers in Molecular Neuroscience|July 22, 2021
Knockdown of Dehydrodolichyl Diphosphate Synthase in the <i>Drosophila</i> Retina Leads to a Unique Pattern of Retinal DegenerationTal Brandwine, Reut Ifrah, Tzofia Bialistoky, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Investigative Ophthalmology & Visual Science|March 12, 2010
Variable retinal phenotypes caused by mutations in the X-linked photopigment gene arrayLiliana Mizrahi-Meissonnier, Saul Merin, Eyal Banin, et al.
American Journal of Ophthalmology|May 29, 2012
Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in DenmarkHanna Bitner, Patrik Schatz, Liliana Mizrahi-Meissonnier, et al.
Investigative Ophthalmology & Visual Science|April 7, 2011
A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive modeHanna Bitner, Liliana Mizrahi-Meissonnier, Gabriel Griefner, et al.
Prenatal Diagnosis|July 24, 2009
Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli familiesAda Rosenmann, Idit Bejarano-Achache, Dalia Eli, et al.
Molecular Vision|May 19, 2012
A tapetal-like fundus reflex in a healthy male: evidence against a role in the pathophysiology of retinal degeneration?Patrik Schatz, Jesper Bregnhøj, Henrik Arvidsson, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like diseaseAnat Beit-Ya'acov, Liliana Mizrahi-Meissonnier, Alexey Obolensky, et al.
Journal of Medical Genetics|May 1, 2014
A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndromeSamer Khateb, Lina Zelinger, Liliana Mizrahi-Meissonnier, et al.
American Journal of Medical Genetics. Part A|May 8, 2007
A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosaEyal Banin, Liliana Mizrahi-Meissonnier, Ruhama Neis, et al.
American Journal of Ophthalmology|December 19, 2013
Ocular phenotype analysis of a family with biallelic mutations in the BEST1 geneDror Sharon, Sermed Al-Hamdani, Karl Engelsberg, et al.
Frontiers in Molecular Neuroscience|July 22, 2021
Knockdown of Dehydrodolichyl Diphosphate Synthase in the <i>Drosophila</i> Retina Leads to a Unique Pattern of Retinal DegenerationTal Brandwine, Reut Ifrah, Tzofia Bialistoky, et al.
Pageof 2