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Marc M Abitbol

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

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Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 14, 2014
Novel insights provided by spectral-domain coherent tomography in pediatric ophthalmologyMarc M Abitbol
Investigative Ophthalmology & Visual Science|February 7, 2015
Networks of genes governing the development of optic and otic vesicles: implications for eye and ear developmentMarc M Abitbol
Investigative Ophthalmology & Visual Science|June 13, 2015
Homozygous Nonsense Mutations in RBP3 Gene Cause Early-Onset Retinal Dystrophies Associated With High MyopiaMarc M Abitbol
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 21, 2019
Requirement of age-dependent normalization of spectral-domain optical coherent tomography parameters in non-human primates for translational studiesMarc M Abitbol
Retina (Philadelphia, Pa.)|June 10, 2021
RETINAL VASCULAR ABNORMALITIES IN CHILDREN WITH NEUROFIBROMATOSIS TYPE 1Romain Touzé, Marc M Abitbol, Dominique Bremond-Gignac, et al.
Investigative Ophthalmology & Visual Science|April 8, 2022
Function of the Retinal Pigment Epithelium in Patients With Neurofibromatosis Type 1Romain Touzé, Marc M Abitbol, Dominique Bremond-Gignac, et al.
Retina (Philadelphia, Pa.)|July 25, 2022
ReplyRomain Touzé, Marc M Abitbol, Dominique Bremond-Gignac, et al.
Molecular Vision|October 26, 2022
Nestin contributes to laser choroidal and retinal neovascularizationSofiane Miloudi, Maud Valensi, Mohamed El Sanharawi, et al.
American Journal of Human Genetics|April 22, 2008
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndromeDaniel F Schorderet, Olivia Nichini, Gaëlle Boisset, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 19, 2019
Sostdc1 is expressed in all major compartments of developing and adult mammalian eyesMaud Valensi, Gabrielle Goldman, Dominique Marchant, et al.
Pageof 1

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

Sort By:
Pageof 1
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 14, 2014
Novel insights provided by spectral-domain coherent tomography in pediatric ophthalmologyMarc M Abitbol
Investigative Ophthalmology & Visual Science|February 7, 2015
Networks of genes governing the development of optic and otic vesicles: implications for eye and ear developmentMarc M Abitbol
Investigative Ophthalmology & Visual Science|June 13, 2015
Homozygous Nonsense Mutations in RBP3 Gene Cause Early-Onset Retinal Dystrophies Associated With High MyopiaMarc M Abitbol
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 21, 2019
Requirement of age-dependent normalization of spectral-domain optical coherent tomography parameters in non-human primates for translational studiesMarc M Abitbol
Retina (Philadelphia, Pa.)|June 10, 2021
RETINAL VASCULAR ABNORMALITIES IN CHILDREN WITH NEUROFIBROMATOSIS TYPE 1Romain Touzé, Marc M Abitbol, Dominique Bremond-Gignac, et al.
Investigative Ophthalmology & Visual Science|April 8, 2022
Function of the Retinal Pigment Epithelium in Patients With Neurofibromatosis Type 1Romain Touzé, Marc M Abitbol, Dominique Bremond-Gignac, et al.
Retina (Philadelphia, Pa.)|July 25, 2022
ReplyRomain Touzé, Marc M Abitbol, Dominique Bremond-Gignac, et al.
Molecular Vision|October 26, 2022
Nestin contributes to laser choroidal and retinal neovascularizationSofiane Miloudi, Maud Valensi, Mohamed El Sanharawi, et al.
American Journal of Human Genetics|April 22, 2008
Mutation in the human homeobox gene NKX5-3 causes an oculo-auricular syndromeDaniel F Schorderet, Olivia Nichini, Gaëlle Boisset, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 19, 2019
Sostdc1 is expressed in all major compartments of developing and adult mammalian eyesMaud Valensi, Gabrielle Goldman, Dominique Marchant, et al.
Pageof 1