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Isabelle Meunier

Showing results (51-60 of 148) with videos related to

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Ophthalmic Genetics|February 18, 2016
Pattern dystrophy in a female carrier of RP2 mutationDina Misky, Tremeur Guillaumie, Corinne Baudoin, et al.
Scientific Reports|May 31, 2018
The effect of PTC124 on choroideremia fibroblasts and iPSC-derived RPE raises considerations for therapySimona Torriano, Nejla Erkilic, David Baux, et al.
The Journal of Infectious Diseases|February 23, 2010
Assessment of the efficacy of commercially available and candidate vaccines against a pandemic H1N1 2009 virusGary P Kobinger, Isabelle Meunier, Ami Patel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 22, 2020
Late-onset riboflavin transporter deficiency: a treatable mimic of various motor neuropathy aetiologiesChristophe Carreau, Charline Benoit, Guido Ahle, et al.
International Journal of Molecular Sciences|June 19, 2024
Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated RetinopathyZelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, et al.
Plos Pathogens|April 15, 2017
RIPK3 interacts with MAVS to regulate type I IFN-mediated immunity to Influenza A virus infectionJeffrey Downey, Erwan Pernet, François Coulombe, et al.
European Journal of Ophthalmology|May 31, 2011
Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome geneSalah Mohamed Cherif Titah, Isabelle Meunier, Catherine Blanchet, et al.
Scientific Reports|October 17, 2020
Clinical and functional analyses of AIPL1 variants reveal mechanisms of pathogenicity linked to different forms of retinal degenerationAlmudena Sacristan-Reviriego, Hoang Mai Le, Michalis Georgiou, et al.
Ophthalmology|January 29, 2011
Systematic screening of BEST1 and PRPH2 in juvenile and adult vitelliform macular dystrophies: a rationale for molecular analysisIsabelle Meunier, Audrey Sénéchal, Claire-Marie Dhaenens, et al.
American Journal of Ophthalmology|February 3, 2009
Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entityChristian P Hamel, Isabelle Meunier, Carl Arndt, et al.
Pageof 15

Showing results (51-60 of 148) with videos related to

Sort By:
Pageof 15
Ophthalmic Genetics|February 18, 2016
Pattern dystrophy in a female carrier of RP2 mutationDina Misky, Tremeur Guillaumie, Corinne Baudoin, et al.
Scientific Reports|May 31, 2018
The effect of PTC124 on choroideremia fibroblasts and iPSC-derived RPE raises considerations for therapySimona Torriano, Nejla Erkilic, David Baux, et al.
The Journal of Infectious Diseases|February 23, 2010
Assessment of the efficacy of commercially available and candidate vaccines against a pandemic H1N1 2009 virusGary P Kobinger, Isabelle Meunier, Ami Patel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 22, 2020
Late-onset riboflavin transporter deficiency: a treatable mimic of various motor neuropathy aetiologiesChristophe Carreau, Charline Benoit, Guido Ahle, et al.
International Journal of Molecular Sciences|June 19, 2024
Novel and Recurrent Copy Number Variants in <i>ABCA4</i>-Associated RetinopathyZelia Corradi, Claire-Marie Dhaenens, Olivier Grunewald, et al.
Plos Pathogens|April 15, 2017
RIPK3 interacts with MAVS to regulate type I IFN-mediated immunity to Influenza A virus infectionJeffrey Downey, Erwan Pernet, François Coulombe, et al.
European Journal of Ophthalmology|May 31, 2011
Cataract as a phenotypic marker for a mutation in WFS1, the Wolfram syndrome geneSalah Mohamed Cherif Titah, Isabelle Meunier, Catherine Blanchet, et al.
Scientific Reports|October 17, 2020
Clinical and functional analyses of AIPL1 variants reveal mechanisms of pathogenicity linked to different forms of retinal degenerationAlmudena Sacristan-Reviriego, Hoang Mai Le, Michalis Georgiou, et al.
Ophthalmology|January 29, 2011
Systematic screening of BEST1 and PRPH2 in juvenile and adult vitelliform macular dystrophies: a rationale for molecular analysisIsabelle Meunier, Audrey Sénéchal, Claire-Marie Dhaenens, et al.
American Journal of Ophthalmology|February 3, 2009
Extensive macular atrophy with pseudodrusen-like appearance: a new clinical entityChristian P Hamel, Isabelle Meunier, Carl Arndt, et al.
Pageof 15