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Luc Jeanjean

Showing results (11-20 of 16) with videos related to

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Muscle & Nerve|February 14, 2015
Orthoptic and video-oculographic analyses in oculopharyngeal muscular dystrophyDimitri Renard, Adelaide Ferraro, Marie-Celine Lorenzini, et al.
JAMA Neurology|October 24, 2012
Neurologic and vascular abnormalities in Klippel-Trenaunay-Weber syndromeDimitri Renard, Chantal Campello, Guillaume Taieb, et al.
Archives of Neurology|July 16, 2008
Optical coherence tomography in neuromyelitis opticaJérôme de Seze, Frederic Blanc, Luc Jeanjean, et al.
Genes|July 27, 2022
Next-Generation Sequencing Identifies Novel <i>PMPCA</i> Variants in Patients with Late-Onset Dominant Optic AtrophyMajida Charif, Arnaud Chevrollier, Naïg Gueguen, et al.
JAMA Ophthalmology|April 9, 2026
Clinical and Genetic Spectrum of ACO2-Linked Dominant Optic AtrophyCléis Beaulieu, Aymane Bouzidi, Valérie Desquiret-Dumas, et al.
Brain Communications|September 1, 2021
Pathogenic <i>NR2F1</i> variants cause a developmental ocular phenotype recapitulated in a mutant mouse modelNeringa Jurkute, Michele Bertacchi, Gavin Arno, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Muscle & Nerve|February 14, 2015
Orthoptic and video-oculographic analyses in oculopharyngeal muscular dystrophyDimitri Renard, Adelaide Ferraro, Marie-Celine Lorenzini, et al.
JAMA Neurology|October 24, 2012
Neurologic and vascular abnormalities in Klippel-Trenaunay-Weber syndromeDimitri Renard, Chantal Campello, Guillaume Taieb, et al.
Archives of Neurology|July 16, 2008
Optical coherence tomography in neuromyelitis opticaJérôme de Seze, Frederic Blanc, Luc Jeanjean, et al.
Genes|July 27, 2022
Next-Generation Sequencing Identifies Novel <i>PMPCA</i> Variants in Patients with Late-Onset Dominant Optic AtrophyMajida Charif, Arnaud Chevrollier, Naïg Gueguen, et al.
JAMA Ophthalmology|April 9, 2026
Clinical and Genetic Spectrum of ACO2-Linked Dominant Optic AtrophyCléis Beaulieu, Aymane Bouzidi, Valérie Desquiret-Dumas, et al.
Brain Communications|September 1, 2021
Pathogenic <i>NR2F1</i> variants cause a developmental ocular phenotype recapitulated in a mutant mouse modelNeringa Jurkute, Michele Bertacchi, Gavin Arno, et al.
Pageof 2