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

Elise Boulanger-Scemama

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
The British Journal of Ophthalmology|December 4, 2016
Size and vitreomacular attachment of primary full-thickness macular holesElise Philippakis, Franck Amouyal, Aude Couturier, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 2013
Intravitreal dexamethasone implant (Ozurdex) for macular edema secondary to retinitis pigmentosaMayer Srour, Giuseppe Querques, Nicolas Leveziel, et al.
Retina (Philadelphia, Pa.)|January 26, 2018
AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY: When Molecular Genetic Testing Helps Clinical DiagnosisElise Boulanger-Scemama, Jose-Alain Sahel, Saddek Mohand-Said, et al.
Ophthalmic Genetics|August 13, 2014
Ophthalmologic impairment during adulthood in central congenital hypoventilation syndrome: a longitudinal cohort analysis of nine patientsElise Boulanger-Scemama, Christine Fardeau, Christian Straus, et al.
American Journal of Ophthalmology|January 7, 2021
Sickle Cell Maculopathy: Microstructural Analysis Using OCTA and Identification of Genetic, Systemic, and Biological Risk FactorsSelim Fares, Sophie Hajjar, Marc Romana, et al.
Human Mutation|April 17, 2018
MERTK mutation update in inherited retinal diseasesIsabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, et al.
American Journal of Ophthalmology|December 20, 2025
Autosomal Recessive Bestrophinopathy - Phenotypic variability, Natural History, and Genotype-phenotype correlationsLorenzo Bianco, Alessio Antropoli, Elise Boulanger-Scemama, et al.
Biomed Research International|February 19, 2015
Targeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophySaid El Shamieh, Elise Boulanger-Scemama, Marie-Elise Lancelot, et al.
International Journal of Molecular Sciences|October 3, 2019
Phenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod DystrophiesElise Boulanger-Scemama, Saddek Mohand-Saïd, Said El Shamieh, et al.
Orphanet Journal of Rare Diseases|June 25, 2015
Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlationElise Boulanger-Scemama, Said El Shamieh, Vanessa Démontant, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
The British Journal of Ophthalmology|December 4, 2016
Size and vitreomacular attachment of primary full-thickness macular holesElise Philippakis, Franck Amouyal, Aude Couturier, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 2013
Intravitreal dexamethasone implant (Ozurdex) for macular edema secondary to retinitis pigmentosaMayer Srour, Giuseppe Querques, Nicolas Leveziel, et al.
Retina (Philadelphia, Pa.)|January 26, 2018
AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY: When Molecular Genetic Testing Helps Clinical DiagnosisElise Boulanger-Scemama, Jose-Alain Sahel, Saddek Mohand-Said, et al.
Ophthalmic Genetics|August 13, 2014
Ophthalmologic impairment during adulthood in central congenital hypoventilation syndrome: a longitudinal cohort analysis of nine patientsElise Boulanger-Scemama, Christine Fardeau, Christian Straus, et al.
American Journal of Ophthalmology|January 7, 2021
Sickle Cell Maculopathy: Microstructural Analysis Using OCTA and Identification of Genetic, Systemic, and Biological Risk FactorsSelim Fares, Sophie Hajjar, Marc Romana, et al.
Human Mutation|April 17, 2018
MERTK mutation update in inherited retinal diseasesIsabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, et al.
American Journal of Ophthalmology|December 20, 2025
Autosomal Recessive Bestrophinopathy - Phenotypic variability, Natural History, and Genotype-phenotype correlationsLorenzo Bianco, Alessio Antropoli, Elise Boulanger-Scemama, et al.
Biomed Research International|February 19, 2015
Targeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophySaid El Shamieh, Elise Boulanger-Scemama, Marie-Elise Lancelot, et al.
International Journal of Molecular Sciences|October 3, 2019
Phenotype Analysis of Retinal Dystrophies in Light of the Underlying Genetic Defects: Application to Cone and Cone-Rod DystrophiesElise Boulanger-Scemama, Saddek Mohand-Saïd, Said El Shamieh, et al.
Orphanet Journal of Rare Diseases|June 25, 2015
Next-generation sequencing applied to a large French cone and cone-rod dystrophy cohort: mutation spectrum and new genotype-phenotype correlationElise Boulanger-Scemama, Said El Shamieh, Vanessa Démontant, et al.
Pageof 2