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Mitochondrion
|
November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity
Virginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Ocular Immunology and Inflammation
|
January 23, 2025
Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic Presentation
Laurie Mourozeau, Virginie Pichon, Aymane Bouzidi, et al.
Mitochondrion
|
July 27, 2010
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation
Christophe Verny, Naig Guegen, Valerie Desquiret, et al.
Brain : a Journal of Neurology
|
November 1, 2022
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands
Aude Rocatcher, Valérie Desquiret-Dumas, Majida Charif, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 13, 2010
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy
Cédric Lamirel, Julien Cassereau, Isabelle Cochereau, et al.
Neuroimage. Clinical
|
March 1, 2020
Neocortical morphometry in Huntington's disease: Indication of the coexistence of abnormal neurodevelopmental and neurodegenerative processes
Jean-Francois Mangin, Denis Rivière, Edouard Duchesnay, et al.
Neurogenetics
|
April 29, 2014
Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification
Gaël Nicolas, Anne-Claire Richard, Cyril Pottier, et al.
Parkinsonism & Related Disorders
|
September 27, 2025
Comparison of tetrabenazine, tiapride and olanzapine in Huntington's disease: a one-year French randomized multicenter study (Neuro-HD)
Katia Youssov, Etienne Audureau, Jérémie Pariente, et al.
Neuropsychologia
|
June 10, 2011
The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's disease
Philippe Allain, Véronique Gaura, Luciano Fasotti, et al.
Journal of Medical Genetics
|
January 16, 2020
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformations
Françoise Bergametti, Geraldine Viot, Christophe Verny, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 92) with videos related to
Sort By:
Page
of 10
Mitochondrion
|
November 11, 2009
Ethambutol-induced optic neuropathy linked to OPA1 mutation and mitochondrial toxicity
Virginie Guillet, Arnaud Chevrollier, Julien Cassereau, et al.
Ocular Immunology and Inflammation
|
January 23, 2025
Two Cases of ROSAH-Like Syndrome Restricted to the Ophthalmologic Presentation
Laurie Mourozeau, Virginie Pichon, Aymane Bouzidi, et al.
Mitochondrion
|
July 27, 2010
Hereditary spastic paraplegia-like disorder due to a mitochondrial ATP6 gene point mutation
Christophe Verny, Naig Guegen, Valerie Desquiret, et al.
Brain : a Journal of Neurology
|
November 1, 2022
The top 10 most frequently involved genes in hereditary optic neuropathies in 2186 probands
Aude Rocatcher, Valérie Desquiret-Dumas, Majida Charif, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 13, 2010
Papilloedema and MRI enhancement of the prechiasmal optic nerve at the acute stage of Leber hereditary optic neuropathy
Cédric Lamirel, Julien Cassereau, Isabelle Cochereau, et al.
Neuroimage. Clinical
|
March 1, 2020
Neocortical morphometry in Huntington's disease: Indication of the coexistence of abnormal neurodevelopmental and neurodegenerative processes
Jean-Francois Mangin, Denis Rivière, Edouard Duchesnay, et al.
Neurogenetics
|
April 29, 2014
Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification
Gaël Nicolas, Anne-Claire Richard, Cyril Pottier, et al.
Parkinsonism & Related Disorders
|
September 27, 2025
Comparison of tetrabenazine, tiapride and olanzapine in Huntington's disease: a one-year French randomized multicenter study (Neuro-HD)
Katia Youssov, Etienne Audureau, Jérémie Pariente, et al.
Neuropsychologia
|
June 10, 2011
The neural substrates of script knowledge deficits as revealed by a PET study in Huntington's disease
Philippe Allain, Véronique Gaura, Luciano Fasotti, et al.
Journal of Medical Genetics
|
January 16, 2020
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformations
Françoise Bergametti, Geraldine Viot, Christophe Verny, et al.
Page
of 10