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Monique Cordonnier

Showing results (1-10 of 14) with videos related to

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Comprehensive Ophthalmology Update|May 20, 2006
Screening for refractive errors in childrenMonique Cordonnier
Acta Neurologica Belgica|March 12, 2013
Neuro-ophthalmological emergencies: which ocular signs or symptoms for which diseases?Monique Cordonnier, Christian Van Nechel
Translational Vision Science & Technology|April 13, 2022
Evaluation of the Blinq Vision Screener in the Detection of Amblyopia and Strabismus in ChildrenArnaud Devlieger, Abdelhakim Youssfi, Monique Cordonnier
American Journal of Medical Genetics. Part A|November 20, 2004
Congenital stationary night blindness: report of an autosomal recessive family and linkage analysisMarc J Abramowicz, Pascale Ribai, Monique Cordonnier
European Journal of Ophthalmology|November 4, 2020
Post-surgical left oculomotor nerve neuromyotonia: Cause or coincidence?Cédric Ballez, Laurent Deleu, Alionka Bostan, et al.
AJNR. American Journal of Neuroradiology|October 27, 2004
An unusual cause of visual loss: involvement of bilateral lateral geniculate bodiesPierre R Lefèbvre, Monique Cordonnier, Danielle Balériaux, et al.
Acta Neurologica Belgica|May 20, 2017
Sixth cranial nerve neuromyotonia mimicking intermittent Duane syndrome type II: case reportAurélie Taylor, Hatice Buruklar, Christian Van Nechel, et al.
BMJ Case Reports|September 21, 2011
Optic neuropathy, renal failure and pulmonary sarcoidosis in a 50-year-old man: where is the link?Laurence Buisseret, Nacima Kisma, Annick Massart, et al.
Molecular Vision|July 21, 2012
TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophyJulie Désir, Frauke Coppieters, Nicole Van Regemorter, et al.
Ophthalmic Genetics|March 18, 2020
Three cases of molecularly confirmed Knobloch syndromeIrina Balikova, Nuri Serdal Sanak, Depasse Fanny, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Comprehensive Ophthalmology Update|May 20, 2006
Screening for refractive errors in childrenMonique Cordonnier
Acta Neurologica Belgica|March 12, 2013
Neuro-ophthalmological emergencies: which ocular signs or symptoms for which diseases?Monique Cordonnier, Christian Van Nechel
Translational Vision Science & Technology|April 13, 2022
Evaluation of the Blinq Vision Screener in the Detection of Amblyopia and Strabismus in ChildrenArnaud Devlieger, Abdelhakim Youssfi, Monique Cordonnier
American Journal of Medical Genetics. Part A|November 20, 2004
Congenital stationary night blindness: report of an autosomal recessive family and linkage analysisMarc J Abramowicz, Pascale Ribai, Monique Cordonnier
European Journal of Ophthalmology|November 4, 2020
Post-surgical left oculomotor nerve neuromyotonia: Cause or coincidence?Cédric Ballez, Laurent Deleu, Alionka Bostan, et al.
AJNR. American Journal of Neuroradiology|October 27, 2004
An unusual cause of visual loss: involvement of bilateral lateral geniculate bodiesPierre R Lefèbvre, Monique Cordonnier, Danielle Balériaux, et al.
Acta Neurologica Belgica|May 20, 2017
Sixth cranial nerve neuromyotonia mimicking intermittent Duane syndrome type II: case reportAurélie Taylor, Hatice Buruklar, Christian Van Nechel, et al.
BMJ Case Reports|September 21, 2011
Optic neuropathy, renal failure and pulmonary sarcoidosis in a 50-year-old man: where is the link?Laurence Buisseret, Nacima Kisma, Annick Massart, et al.
Molecular Vision|July 21, 2012
TMEM126A mutation in a Moroccan family with autosomal recessive optic atrophyJulie Désir, Frauke Coppieters, Nicole Van Regemorter, et al.
Ophthalmic Genetics|March 18, 2020
Three cases of molecularly confirmed Knobloch syndromeIrina Balikova, Nuri Serdal Sanak, Depasse Fanny, et al.
Pageof 2