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Thierry Maisonobe

Showing results (51-60 of 130) with videos related to

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Journal of Neurology|February 3, 2011
Mononeuropathy multiplex associated with acute parvovirus B19 infection: characteristics, treatment and outcomeTimothée Lenglet, Julien Haroche, Aurélie Schnuriger, et al.
Muscle & Nerve|January 23, 2025
Electrophysiological Abnormalities in Finger Extension Weakness and DOwnbeat Nystagmus Motor Neuron Disease: Three New Patients and Review of the LiteratureJulian Theuriet, Emilien Bernard, Nathalie Guy, et al.
Journal of the Peripheral Nervous System : JPNS|May 20, 2024
A previously unreported NARS1 variant causes dominant distal hereditary motor neuropathy in a French familyJulian Theuriet, Sheila Marte, Arnaud Isapof, et al.
Brain : a Journal of Neurology|February 4, 2006
Shared blood and muscle CD8+ T-cell expansions in inclusion body myositisDalia Dimitri, Olivier Benveniste, Odile Dubourg, et al.
Cardiology|June 29, 2006
Cardiomyopathy related to antimalarial therapy with illustrative case reportNathalie Costedoat-Chalumeau, Jean-Sebastien Hulot, Zahir Amoura, et al.
Journal of Neurology|May 25, 2017
Clinicopathological features of multiple mononeuropathy associated with systemic lupus erythematosus: a multicenter studyElodie Rivière, Fleur Cohen Aubart, Thierry Maisonobe, et al.
Brain : a Journal of Neurology|July 23, 2015
Anti-Jo-1 antibody-positive patients show a characteristic necrotizing perifascicular myositisLénaig Mescam-Mancini, Yves Allenbach, Baptiste Hervier, et al.
The Oncologist|October 17, 2019
Guillain-Barré Syndrome During Platinum-Based Chemotherapy: A Case Series and Review of the LiteratureEvangelia Pappa, Giulia Berzero, Bastien Herlin, et al.
Archives of Neurology|April 23, 2003
Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 geneNazha Birouk, Hamid Azzedine, Odile Dubourg, et al.
Neuromuscular Disorders : NMD|July 10, 2021
Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT diseaseRocio-Nur Villar-Quiles, Van Thuy Le, Sarah Leonard-Louis, et al.
Pageof 13

Showing results (51-60 of 130) with videos related to

Sort By:
Pageof 13
Journal of Neurology|February 3, 2011
Mononeuropathy multiplex associated with acute parvovirus B19 infection: characteristics, treatment and outcomeTimothée Lenglet, Julien Haroche, Aurélie Schnuriger, et al.
Muscle & Nerve|January 23, 2025
Electrophysiological Abnormalities in Finger Extension Weakness and DOwnbeat Nystagmus Motor Neuron Disease: Three New Patients and Review of the LiteratureJulian Theuriet, Emilien Bernard, Nathalie Guy, et al.
Journal of the Peripheral Nervous System : JPNS|May 20, 2024
A previously unreported NARS1 variant causes dominant distal hereditary motor neuropathy in a French familyJulian Theuriet, Sheila Marte, Arnaud Isapof, et al.
Brain : a Journal of Neurology|February 4, 2006
Shared blood and muscle CD8+ T-cell expansions in inclusion body myositisDalia Dimitri, Olivier Benveniste, Odile Dubourg, et al.
Cardiology|June 29, 2006
Cardiomyopathy related to antimalarial therapy with illustrative case reportNathalie Costedoat-Chalumeau, Jean-Sebastien Hulot, Zahir Amoura, et al.
Journal of Neurology|May 25, 2017
Clinicopathological features of multiple mononeuropathy associated with systemic lupus erythematosus: a multicenter studyElodie Rivière, Fleur Cohen Aubart, Thierry Maisonobe, et al.
Brain : a Journal of Neurology|July 23, 2015
Anti-Jo-1 antibody-positive patients show a characteristic necrotizing perifascicular myositisLénaig Mescam-Mancini, Yves Allenbach, Baptiste Hervier, et al.
The Oncologist|October 17, 2019
Guillain-Barré Syndrome During Platinum-Based Chemotherapy: A Case Series and Review of the LiteratureEvangelia Pappa, Giulia Berzero, Bastien Herlin, et al.
Archives of Neurology|April 23, 2003
Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 geneNazha Birouk, Hamid Azzedine, Odile Dubourg, et al.
Neuromuscular Disorders : NMD|July 10, 2021
Leukoencephalopathy and conduction blocks in PLEKHG5-associated intermediate CMT diseaseRocio-Nur Villar-Quiles, Van Thuy Le, Sarah Leonard-Louis, et al.
Pageof 13