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Benoît Funalot

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Medecine Sciences : M/S|October 9, 2010
[Charcot-Marie-Tooth (CMT) disease: an update]Jean-Michel Vallat, Benoît Funalot
Acta Neuropathologica|February 5, 2011
Nerve biopsy: requirements for diagnosis and clinical valueJean-Michel Vallat, Benoît Funalot, Laurent Magy
Current Opinion in Neurology|August 16, 2013
The various Charcot-Marie-Tooth diseasesJean-Michel Vallat, Stéphane Mathis, Benoît Funalot
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 28, 2014
Characterization of Endoneurial Fibroblast-like Cells from Human and Rat Peripheral NervesLaurence Richard, Nicolas Védrenne, Jean-Michel Vallat, et al.
Bulletin De L'Academie Nationale De Medecine|July 3, 2013
[Familial amyloidotic polyneuropathies]Jean-Michel Vallat, Benoît Funalot, Frédéric Faugeras, et al.
Presse Medicale (Paris, France : 1983)|March 31, 2009
[Hereditary peripheral neuropathies]Jean-Michel Vallat, Mériem Tazir, Judith Calvo, et al.
AME Case Reports|April 13, 2026
Adult case of 17β-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency due to the p. Arg130Cys mutation of the <i>HSD17B10</i> gene: case reportAlyaa Khodawrdi, Chadia Mekki, Ariane Lunati-Rozie, et al.
Frontiers in Neurology|June 9, 2025
Clinical and cognitive assessment in Friedreich ataxia clinical trials: a reviewÁlvaro Darriba, Arnold Munnich, Pedro Cardoso-Leite, et al.
Bulletin De L'Academie Nationale De Medecine|September 2, 2009
[Ultrastructural lesions of axonal mitochondria in patients with childhood-onset Charcot-Marie-Tooth disease due to MFN2 mutations]Benoît Funalot, Corinne Magdelaine, Franck Sturtz, et al.
Genetic Testing|January 27, 2007
Genetic screening for two LRRK2 mutations in French patients with idiopathic Parkinson's diseaseBenoît Funalot, William C Nichols, Jordi Pérez-Tur, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Medecine Sciences : M/S|October 9, 2010
[Charcot-Marie-Tooth (CMT) disease: an update]Jean-Michel Vallat, Benoît Funalot
Acta Neuropathologica|February 5, 2011
Nerve biopsy: requirements for diagnosis and clinical valueJean-Michel Vallat, Benoît Funalot, Laurent Magy
Current Opinion in Neurology|August 16, 2013
The various Charcot-Marie-Tooth diseasesJean-Michel Vallat, Stéphane Mathis, Benoît Funalot
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|March 28, 2014
Characterization of Endoneurial Fibroblast-like Cells from Human and Rat Peripheral NervesLaurence Richard, Nicolas Védrenne, Jean-Michel Vallat, et al.
Bulletin De L'Academie Nationale De Medecine|July 3, 2013
[Familial amyloidotic polyneuropathies]Jean-Michel Vallat, Benoît Funalot, Frédéric Faugeras, et al.
Presse Medicale (Paris, France : 1983)|March 31, 2009
[Hereditary peripheral neuropathies]Jean-Michel Vallat, Mériem Tazir, Judith Calvo, et al.
AME Case Reports|April 13, 2026
Adult case of 17β-hydroxysteroid dehydrogenase type 10 (HSD10) deficiency due to the p. Arg130Cys mutation of the <i>HSD17B10</i> gene: case reportAlyaa Khodawrdi, Chadia Mekki, Ariane Lunati-Rozie, et al.
Frontiers in Neurology|June 9, 2025
Clinical and cognitive assessment in Friedreich ataxia clinical trials: a reviewÁlvaro Darriba, Arnold Munnich, Pedro Cardoso-Leite, et al.
Bulletin De L'Academie Nationale De Medecine|September 2, 2009
[Ultrastructural lesions of axonal mitochondria in patients with childhood-onset Charcot-Marie-Tooth disease due to MFN2 mutations]Benoît Funalot, Corinne Magdelaine, Franck Sturtz, et al.
Genetic Testing|January 27, 2007
Genetic screening for two LRRK2 mutations in French patients with idiopathic Parkinson's diseaseBenoît Funalot, William C Nichols, Jordi Pérez-Tur, et al.
Pageof 5