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Fanny Mochel

Showing results (21-30 of 172) with videos related to

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Plos One|April 13, 2011
Altered dopamine and serotonin metabolism in motorically asymptomatic R6/2 miceFanny Mochel, Brandon Durant, Alexandra Durr, et al.
Archives of Neurology|February 16, 2011
Validation of plasma branched chain amino acids as biomarkers in Huntington diseaseFanny Mochel, Sandra Benaich, Daniel Rabier, et al.
European Journal of Medical Genetics|January 16, 2008
Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genesFanny Mochel, Chantal Missirian, Rachel Reynaud, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|March 10, 2017
Imaging and spectroscopic approaches to probe brain energy metabolism dysregulation in neurodegenerative diseasesGilles Bonvento, Julien Valette, Julien Flament, et al.
Journal of Inherited Metabolic Disease|November 22, 2014
The clinical spectrum of inherited diseases involved in the synthesis and remodeling of complex lipids. A tentative overviewÀngels Garcia-Cazorla, Fanny Mochel, Foudil Lamari, et al.
Neurology|April 28, 2019
Severe transient myopathy in a patient with progressive multiple sclerosis and high-dose biotinElisabeth Maillart, Fanny Mochel, Cécile Acquaviva, et al.
Journal of Inherited Metabolic Disease|March 19, 2019
Proposal for a simplified classification of IMD based on a pathophysiological approach: A practical guide for cliniciansJean-Marie Saudubray, Fanny Mochel, Foudil Lamari, et al.
Current Biology : CB|August 12, 2022
A neuro-metabolic account of why daylong cognitive work alters the control of economic decisionsAntonius Wiehler, Francesca Branzoli, Isaac Adanyeguh, et al.
Muscle & Nerve|January 27, 2021
Demyelinating motor neuropathy associated with a homozygous GPT2 pathogenic variantLyse Ruaud, Boris Keren, Rabab Debs, et al.
Brain : a Journal of Neurology|August 23, 2015
Reply: ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanismMarie Coutelier, Fanny Mochel, Jean-Marie Saudubray, et al.
Pageof 18

Showing results (21-30 of 172) with videos related to

Sort By:
Pageof 18
Plos One|April 13, 2011
Altered dopamine and serotonin metabolism in motorically asymptomatic R6/2 miceFanny Mochel, Brandon Durant, Alexandra Durr, et al.
Archives of Neurology|February 16, 2011
Validation of plasma branched chain amino acids as biomarkers in Huntington diseaseFanny Mochel, Sandra Benaich, Daniel Rabier, et al.
European Journal of Medical Genetics|January 16, 2008
Normal intelligence and social interactions in a male patient despite the deletion of NLGN4X and the VCX genesFanny Mochel, Chantal Missirian, Rachel Reynaud, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|March 10, 2017
Imaging and spectroscopic approaches to probe brain energy metabolism dysregulation in neurodegenerative diseasesGilles Bonvento, Julien Valette, Julien Flament, et al.
Journal of Inherited Metabolic Disease|November 22, 2014
The clinical spectrum of inherited diseases involved in the synthesis and remodeling of complex lipids. A tentative overviewÀngels Garcia-Cazorla, Fanny Mochel, Foudil Lamari, et al.
Neurology|April 28, 2019
Severe transient myopathy in a patient with progressive multiple sclerosis and high-dose biotinElisabeth Maillart, Fanny Mochel, Cécile Acquaviva, et al.
Journal of Inherited Metabolic Disease|March 19, 2019
Proposal for a simplified classification of IMD based on a pathophysiological approach: A practical guide for cliniciansJean-Marie Saudubray, Fanny Mochel, Foudil Lamari, et al.
Current Biology : CB|August 12, 2022
A neuro-metabolic account of why daylong cognitive work alters the control of economic decisionsAntonius Wiehler, Francesca Branzoli, Isaac Adanyeguh, et al.
Muscle & Nerve|January 27, 2021
Demyelinating motor neuropathy associated with a homozygous GPT2 pathogenic variantLyse Ruaud, Boris Keren, Rabab Debs, et al.
Brain : a Journal of Neurology|August 23, 2015
Reply: ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanismMarie Coutelier, Fanny Mochel, Jean-Marie Saudubray, et al.
Pageof 18