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Fanny Mochel

Showing results (11-20 of 172) with videos related to

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The Journal of Clinical Investigation|February 3, 2011
Energy deficit in Huntington disease: why it mattersFanny Mochel, Ronald G Haller
Journal of Inherited Metabolic Disease|June 10, 2006
Anaplerotic diet therapy in inherited metabolic disease: therapeutic potentialCharles R Roe, Fanny Mochel
Frontiers in Neuroscience|March 18, 2020
Lipids in the Physiopathology of Hereditary Spastic ParaplegiasFrédéric Darios, Fanny Mochel, Giovanni Stevanin
Frontline Gastroenterology|September 2, 2022
Commentary to Aby <i>et al</i>: serum ammonia use - unnecessary, frequent and costlyJohannes Häberle, James Nurse, Fanny Mochel
Clinics and Research in Hepatology and Gastroenterology|February 19, 2019
Domino liver transplantation: the risk of disease recurrenceFiloména Conti, Fanny Mochel, Yvon Calmus
Journal of Inherited Metabolic Disease|September 21, 2014
An overview of inborn errors of complex lipid biosynthesis and remodellingFoudil Lamari, Fanny Mochel, Jean-Marie Saudubray
Neuron|February 22, 2019
Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular TherapiesMatthis Synofzik, Hélène Puccio, Fanny Mochel, et al.
Current Opinion in Neurology|July 14, 2020
MRI of neurodegeneration with brain iron accumulationStéphane Lehéricy, Emmanuel Roze, Cyril Goizet, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2024
Comment to: "Randomized Phase 3 Study of Triheptanoin for Glut1 Deficiency Syndrome-Associated Paroxysmal Movement Disorders"Emmanuel Roze, Aurélie Méneret, Elodie Hainque, et al.
Frontiers in Molecular Biosciences|August 16, 2024
Innovative tree-based method for sampling molecular conformations: exploring the ATP-binding cassette subfamily D member 1 (ABCD1) transporter as a case studyThomas Haschka, Foudil Lamari, Fanny Mochel, et al.
Pageof 18

Showing results (11-20 of 172) with videos related to

Sort By:
Pageof 18
The Journal of Clinical Investigation|February 3, 2011
Energy deficit in Huntington disease: why it mattersFanny Mochel, Ronald G Haller
Journal of Inherited Metabolic Disease|June 10, 2006
Anaplerotic diet therapy in inherited metabolic disease: therapeutic potentialCharles R Roe, Fanny Mochel
Frontiers in Neuroscience|March 18, 2020
Lipids in the Physiopathology of Hereditary Spastic ParaplegiasFrédéric Darios, Fanny Mochel, Giovanni Stevanin
Frontline Gastroenterology|September 2, 2022
Commentary to Aby <i>et al</i>: serum ammonia use - unnecessary, frequent and costlyJohannes Häberle, James Nurse, Fanny Mochel
Clinics and Research in Hepatology and Gastroenterology|February 19, 2019
Domino liver transplantation: the risk of disease recurrenceFiloména Conti, Fanny Mochel, Yvon Calmus
Journal of Inherited Metabolic Disease|September 21, 2014
An overview of inborn errors of complex lipid biosynthesis and remodellingFoudil Lamari, Fanny Mochel, Jean-Marie Saudubray
Neuron|February 22, 2019
Autosomal Recessive Cerebellar Ataxias: Paving the Way toward Targeted Molecular TherapiesMatthis Synofzik, Hélène Puccio, Fanny Mochel, et al.
Current Opinion in Neurology|July 14, 2020
MRI of neurodegeneration with brain iron accumulationStéphane Lehéricy, Emmanuel Roze, Cyril Goizet, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2024
Comment to: "Randomized Phase 3 Study of Triheptanoin for Glut1 Deficiency Syndrome-Associated Paroxysmal Movement Disorders"Emmanuel Roze, Aurélie Méneret, Elodie Hainque, et al.
Frontiers in Molecular Biosciences|August 16, 2024
Innovative tree-based method for sampling molecular conformations: exploring the ATP-binding cassette subfamily D member 1 (ABCD1) transporter as a case studyThomas Haschka, Foudil Lamari, Fanny Mochel, et al.
Pageof 18