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Movement Disorders : Official Journal of the Movement Disorder Society
|
February 15, 2024
Stochastic Optical Reconstruction Microscopy Imaging of Multiple System Atrophy Inclusions Suggests Stepwise α-Synuclein Aggregation
Benoît Vovard, Alexia Bodin, Julien Gouju, et al.
Brain : a Journal of Neurology
|
July 6, 2023
Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells
Alexia Bodin, Logan Greibill, Julien Gouju, et al.
Plos One
|
September 15, 2016
Insulin-Like Growth Factor-1 but Not Insulin Predicts Cognitive Decline in Huntington's Disease
Linda Salem, Nadine Saleh, Gaelle Désaméricq, et al.
Brain : a Journal of Neurology
|
September 9, 2006
Phenotype associated with APP duplication in five families
Lucie Cabrejo, Lucie Guyant-Maréchal, Annie Laquerrière, et al.
Annals of Neurology
|
April 21, 2007
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease
Dominique Loiseau, Arnaud Chevrollier, Christophe Verny, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
March 1, 2012
pH as a biomarker of neurodegeneration in Huntington's disease: a translational rodent-human MRS study
Myriam M Chaumeil, Julien Valette, Céline Baligand, et al.
Annals of Neurology
|
May 23, 2008
Hereditary optic neuropathies share a common mitochondrial coupling defect
Arnaud Chevrollier, Virginie Guillet, Dominique Loiseau, et al.
The International Journal of Biochemistry & Cell Biology
|
May 31, 2015
Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency
Géraldine Leman, Naïg Gueguen, Valérie Desquiret-Dumas, et al.
Human Mutation
|
March 26, 2009
Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations
Marc Ferré, Dominique Bonneau, Dan Milea, et al.
Frontiers in Neurology
|
July 24, 2019
International Guidelines for the Treatment of Huntington's Disease
Anne-Catherine Bachoud-Lévi, Joaquim Ferreira, Renaud Massart, et al.
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of 10
Search research articles
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Showing results (61-70 of 92) with videos related to
Sort By:
Page
of 10
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 15, 2024
Stochastic Optical Reconstruction Microscopy Imaging of Multiple System Atrophy Inclusions Suggests Stepwise α-Synuclein Aggregation
Benoît Vovard, Alexia Bodin, Julien Gouju, et al.
Brain : a Journal of Neurology
|
July 6, 2023
Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells
Alexia Bodin, Logan Greibill, Julien Gouju, et al.
Plos One
|
September 15, 2016
Insulin-Like Growth Factor-1 but Not Insulin Predicts Cognitive Decline in Huntington's Disease
Linda Salem, Nadine Saleh, Gaelle Désaméricq, et al.
Brain : a Journal of Neurology
|
September 9, 2006
Phenotype associated with APP duplication in five families
Lucie Cabrejo, Lucie Guyant-Maréchal, Annie Laquerrière, et al.
Annals of Neurology
|
April 21, 2007
Mitochondrial coupling defect in Charcot-Marie-Tooth type 2A disease
Dominique Loiseau, Arnaud Chevrollier, Christophe Verny, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
March 1, 2012
pH as a biomarker of neurodegeneration in Huntington's disease: a translational rodent-human MRS study
Myriam M Chaumeil, Julien Valette, Céline Baligand, et al.
Annals of Neurology
|
May 23, 2008
Hereditary optic neuropathies share a common mitochondrial coupling defect
Arnaud Chevrollier, Virginie Guillet, Dominique Loiseau, et al.
The International Journal of Biochemistry & Cell Biology
|
May 31, 2015
Assembly defects induce oxidative stress in inherited mitochondrial complex I deficiency
Géraldine Leman, Naïg Gueguen, Valérie Desquiret-Dumas, et al.
Human Mutation
|
March 26, 2009
Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations
Marc Ferré, Dominique Bonneau, Dan Milea, et al.
Frontiers in Neurology
|
July 24, 2019
International Guidelines for the Treatment of Huntington's Disease
Anne-Catherine Bachoud-Lévi, Joaquim Ferreira, Renaud Massart, et al.
Page
of 10