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Patrizia Amati-Bonneau

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 20, 2026
Melas mimicking hydrocephalusMatthieu Labriffe, Patrizia Amati-Bonneau, Marco Spinazzi
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|April 18, 2025
Toxic ethambuthol-induced optic neuropathy in a patient with OPA1 mutationClaire Meyniel, Patrizia Amati-Bonneau, Pascal Reynier, et al.
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.
Journal of Inherited Metabolic Disease|November 27, 2024
Uncommon case of mitochondrial disease: Mild amyotrophy of the legs and symmetrical lipomatosis of the armsLeslie Bercu, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, 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.
The British Journal of Ophthalmology|August 3, 2010
Never too old to harbour a young man's disease?Sylvia Giraudet, Cédric Lamirel, Patrizia Amati-Bonneau, 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.
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.
Pageof 11

Showing results (1-10 of 105) with videos related to

Sort By:
Pageof 11
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 20, 2026
Melas mimicking hydrocephalusMatthieu Labriffe, Patrizia Amati-Bonneau, Marco Spinazzi
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|April 18, 2025
Toxic ethambuthol-induced optic neuropathy in a patient with OPA1 mutationClaire Meyniel, Patrizia Amati-Bonneau, Pascal Reynier, et al.
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.
Journal of Inherited Metabolic Disease|November 27, 2024
Uncommon case of mitochondrial disease: Mild amyotrophy of the legs and symmetrical lipomatosis of the armsLeslie Bercu, Patrizia Amati-Bonneau, Valérie Desquiret-Dumas, 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.
The British Journal of Ophthalmology|August 3, 2010
Never too old to harbour a young man's disease?Sylvia Giraudet, Cédric Lamirel, Patrizia Amati-Bonneau, 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.
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.
Pageof 11