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C Desnuelle

Showing results (71-80 of 118) with videos related to

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Journal of Medical Genetics|July 17, 2008
Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patientsL Davidovic, S Sacconi, E G Bechara, et al.
Presse Medicale (Paris, France : 1983)|March 3, 1990
[An unusual association of myasthenia and T8 lymphoid leukemia]G Kaplanski, C Desnuelle, J R Harle, et al.
Genomics|September 23, 1997
Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 geneV Paquis-Flucklinger, S Santucci-Darmanin, R Paul, et al.
Revue Neurologique|January 1, 1991
[Slowly progressive myopathy with accumulation of tubular aggregates]D Figarella-Branger, J F Pellissier, A M Perez-Castillo, et al.
Revue Neurologique|January 14, 2014
[Efficacy of autologous peripheral blood stem cell transplantation (auto-PBSCT) on the neuropathic manifestations in POEMS syndrome]S Gronier, E Delmont, L Legros, et al.
La Revue De Medecine Interne|September 1, 1992
[Ptosis and asthenia manifesting a mitochondrial myopathy]P Disdier, J R Harlé, D Figarella-Branger, et al.
Revue Neurologique|April 18, 2026
Treatment pathway, healthcare resource utilization and direct cost of ALS in France: A nationwide claims database studyC Desnuelle, P Couratier, P Corcia, et al.
The American Journal of Medicine|February 1, 1992
Polymyalgia rheumatica and mitochondrial myopathy: clinicopathologic and biochemical studies in five casesJ R Harle, J F Pellissier, C Desnuelle, et al.
Revue Neurologique|January 1, 1991
[Anomaly in the neurotransmitter amino acids in amyotrophic lateral sclerosis: a therapeutic application]O Blin, C Desnuelle, C Guelton, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu|January 1, 1997
[Detection and prevalence of mitochondrial genome mutations in diabetes]V Paquis-Flucklinger, B Vialettes, B Canivet, et al.
Pageof 12

Showing results (71-80 of 118) with videos related to

Sort By:
Pageof 12
Journal of Medical Genetics|July 17, 2008
Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patientsL Davidovic, S Sacconi, E G Bechara, et al.
Presse Medicale (Paris, France : 1983)|March 3, 1990
[An unusual association of myasthenia and T8 lymphoid leukemia]G Kaplanski, C Desnuelle, J R Harle, et al.
Genomics|September 23, 1997
Cloning and expression analysis of a meiosis-specific MutS homolog: the human MSH4 geneV Paquis-Flucklinger, S Santucci-Darmanin, R Paul, et al.
Revue Neurologique|January 1, 1991
[Slowly progressive myopathy with accumulation of tubular aggregates]D Figarella-Branger, J F Pellissier, A M Perez-Castillo, et al.
Revue Neurologique|January 14, 2014
[Efficacy of autologous peripheral blood stem cell transplantation (auto-PBSCT) on the neuropathic manifestations in POEMS syndrome]S Gronier, E Delmont, L Legros, et al.
La Revue De Medecine Interne|September 1, 1992
[Ptosis and asthenia manifesting a mitochondrial myopathy]P Disdier, J R Harlé, D Figarella-Branger, et al.
Revue Neurologique|April 18, 2026
Treatment pathway, healthcare resource utilization and direct cost of ALS in France: A nationwide claims database studyC Desnuelle, P Couratier, P Corcia, et al.
The American Journal of Medicine|February 1, 1992
Polymyalgia rheumatica and mitochondrial myopathy: clinicopathologic and biochemical studies in five casesJ R Harle, J F Pellissier, C Desnuelle, et al.
Revue Neurologique|January 1, 1991
[Anomaly in the neurotransmitter amino acids in amyotrophic lateral sclerosis: a therapeutic application]O Blin, C Desnuelle, C Guelton, et al.
Journees Annuelles De Diabetologie De L'Hotel-Dieu|January 1, 1997
[Detection and prevalence of mitochondrial genome mutations in diabetes]V Paquis-Flucklinger, B Vialettes, B Canivet, et al.
Pageof 12