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Matthieu Labriffe
Patrizia Amati-Bonneau
Marco Spinazzi

Showing results (1-10 of 156) with videos related to

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Current Opinion in Neurology|November 17, 2009
Genetically determined optic neuropathiesDan Milea, Patrizia Amati-Bonneau, Pascal Reynier, et al.
Human Mutation|April 16, 2005
eOPA1: an online database for OPA1 mutationsMarc Ferré, Patrizia Amati-Bonneau, Yves Tourmen, et al.
American Journal of Ophthalmology|December 4, 2003
The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 genePatrizia Amati-Bonneau, Sylvie Odent, Christelle Derrien, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|July 7, 2018
Retinal Neuronal Loss in Visually Asymptomatic Patients With Myoclonic Epilepsy With Ragged-Red FibersRaymond P Najjar, Pascal Reynier, Angélique Caignard, et al.
Orphanet Journal of Rare Diseases|July 11, 2012
Dominant optic atrophyGuy Lenaers, Christian Hamel, Cécile Delettre, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|May 14, 2020
Normal and pathological imaging of the hippocampus in geriatric patientsDamien Combes, Jean-Yves Tanguy, Cédric Annweiler, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|September 27, 2019
[Normal and pathological hippocampal imaging in geriatric patients]Damien Combes, Jean-Yves Tanguy, Cédric Annweiler, et al.
Seminars in Cell & Developmental Biology|August 10, 2016
PARL: The mitochondrial rhomboid proteaseMarco Spinazzi, Bart De Strooper
Neurobiology of Disease|April 26, 2026
Analysis of mitochondrial DNA heteroplasmy in sporadic ALS suggests technical limitations rather than disease associationPhilippe Codron, Valérie Desquiret, Delphine Prunier, et al.
BMC Medical Genetics|July 22, 2009
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA backgroundDenis Pierron, Marc Ferré, Christophe Rocher, et al.
Pageof 16

Showing results (1-10 of 156) with videos related to

Sort By:
Pageof 16
Current Opinion in Neurology|November 17, 2009
Genetically determined optic neuropathiesDan Milea, Patrizia Amati-Bonneau, Pascal Reynier, et al.
Human Mutation|April 16, 2005
eOPA1: an online database for OPA1 mutationsMarc Ferré, Patrizia Amati-Bonneau, Yves Tourmen, et al.
American Journal of Ophthalmology|December 4, 2003
The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 genePatrizia Amati-Bonneau, Sylvie Odent, Christelle Derrien, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|July 7, 2018
Retinal Neuronal Loss in Visually Asymptomatic Patients With Myoclonic Epilepsy With Ragged-Red FibersRaymond P Najjar, Pascal Reynier, Angélique Caignard, et al.
Orphanet Journal of Rare Diseases|July 11, 2012
Dominant optic atrophyGuy Lenaers, Christian Hamel, Cécile Delettre, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|May 14, 2020
Normal and pathological imaging of the hippocampus in geriatric patientsDamien Combes, Jean-Yves Tanguy, Cédric Annweiler, et al.
Geriatrie Et Psychologie Neuropsychiatrie Du Vieillissement|September 27, 2019
[Normal and pathological hippocampal imaging in geriatric patients]Damien Combes, Jean-Yves Tanguy, Cédric Annweiler, et al.
Seminars in Cell & Developmental Biology|August 10, 2016
PARL: The mitochondrial rhomboid proteaseMarco Spinazzi, Bart De Strooper
Neurobiology of Disease|April 26, 2026
Analysis of mitochondrial DNA heteroplasmy in sporadic ALS suggests technical limitations rather than disease associationPhilippe Codron, Valérie Desquiret, Delphine Prunier, et al.
BMC Medical Genetics|July 22, 2009
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA backgroundDenis Pierron, Marc Ferré, Christophe Rocher, et al.
Pageof 16