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Plos One
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April 13, 2011
Altered dopamine and serotonin metabolism in motorically asymptomatic R6/2 mice
Fanny Mochel, Brandon Durant, Alexandra Durr, et al.
Archives of Neurology
|
February 16, 2011
Validation of plasma branched chain amino acids as biomarkers in Huntington disease
Fanny 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 genes
Fanny 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 diseases
Gilles 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 overview
Àngels 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 biotin
Elisabeth 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 clinicians
Jean-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 decisions
Antonius Wiehler, Francesca Branzoli, Isaac Adanyeguh, et al.
Muscle & Nerve
|
January 27, 2021
Demyelinating motor neuropathy associated with a homozygous GPT2 pathogenic variant
Lyse 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 mechanism
Marie Coutelier, Fanny Mochel, Jean-Marie Saudubray, et al.
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of 18
Search research articles
Search
Showing results (21-30 of 172) with videos related to
Sort By:
Page
of 18
Plos One
|
April 13, 2011
Altered dopamine and serotonin metabolism in motorically asymptomatic R6/2 mice
Fanny Mochel, Brandon Durant, Alexandra Durr, et al.
Archives of Neurology
|
February 16, 2011
Validation of plasma branched chain amino acids as biomarkers in Huntington disease
Fanny 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 genes
Fanny 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 diseases
Gilles 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 overview
Àngels 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 biotin
Elisabeth 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 clinicians
Jean-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 decisions
Antonius Wiehler, Francesca Branzoli, Isaac Adanyeguh, et al.
Muscle & Nerve
|
January 27, 2021
Demyelinating motor neuropathy associated with a homozygous GPT2 pathogenic variant
Lyse 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 mechanism
Marie Coutelier, Fanny Mochel, Jean-Marie Saudubray, et al.
Page
of 18