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Thierry Maisonobe

Showing results (121-130 of 130) with videos related to

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Brain Communications|August 17, 2021
The wide spectrum of COVID-19 neuropsychiatric complications within a multidisciplinary centreCécile Delorme, Marion Houot, Charlotte Rosso, et al.
Journal of Neurology|July 18, 2020
Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 seraEmilien Delmont, Alexandre Brodovitch, Ludivine Kouton, et al.
Medicine|May 7, 2014
Anti-HMGCR autoantibodies in European patients with autoimmune necrotizing myopathies: inconstant exposure to statinYves Allenbach, Laurent Drouot, Aude Rigolet, et al.
Brain : a Journal of Neurology|August 28, 2024
Dysregulation of muscle cholesterol transport in amyotrophic lateral sclerosisDelphine Sapaly, Flore Cheguillaume, Laure Weill, et al.
Journal of Cachexia, Sarcopenia and Muscle|February 23, 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesiclesLaura Le Gall, William J Duddy, Cecile Martinat, et al.
Brain : a Journal of Neurology|February 11, 2020
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansionAndrea Cortese, Stefano Tozza, Wai Yan Yau, et al.
Cancer Discovery|February 23, 2023
Abatacept/Ruxolitinib and Screening for Concomitant Respiratory Muscle Failure to Mitigate Fatality of Immune-Checkpoint Inhibitor MyocarditisJoe-Elie Salem, Marie Bretagne, Baptiste Abbar, et al.
American Journal of Human Genetics|October 18, 2016
Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar DisorganizationGina L O'Grady, Heather A Best, Tamar E Sztal, et al.
Nature Genetics|May 28, 2020
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
Nature Genetics|May 6, 2020
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
Pageof 13

Showing results (121-130 of 130) with videos related to

Sort By:
Pageof 13
You have reached the last page of results.This site can display upto 130 results.
Brain Communications|August 17, 2021
The wide spectrum of COVID-19 neuropsychiatric complications within a multidisciplinary centreCécile Delorme, Marion Houot, Charlotte Rosso, et al.
Journal of Neurology|July 18, 2020
Antibodies against the node of Ranvier: a real-life evaluation of incidence, clinical features and response to treatment based on a prospective analysis of 1500 seraEmilien Delmont, Alexandre Brodovitch, Ludivine Kouton, et al.
Medicine|May 7, 2014
Anti-HMGCR autoantibodies in European patients with autoimmune necrotizing myopathies: inconstant exposure to statinYves Allenbach, Laurent Drouot, Aude Rigolet, et al.
Brain : a Journal of Neurology|August 28, 2024
Dysregulation of muscle cholesterol transport in amyotrophic lateral sclerosisDelphine Sapaly, Flore Cheguillaume, Laure Weill, et al.
Journal of Cachexia, Sarcopenia and Muscle|February 23, 2022
Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesiclesLaura Le Gall, William J Duddy, Cecile Martinat, et al.
Brain : a Journal of Neurology|February 11, 2020
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome due to RFC1 repeat expansionAndrea Cortese, Stefano Tozza, Wai Yan Yau, et al.
Cancer Discovery|February 23, 2023
Abatacept/Ruxolitinib and Screening for Concomitant Respiratory Muscle Failure to Mitigate Fatality of Immune-Checkpoint Inhibitor MyocarditisJoe-Elie Salem, Marie Bretagne, Baptiste Abbar, et al.
American Journal of Human Genetics|October 18, 2016
Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar DisorganizationGina L O'Grady, Heather A Best, Tamar E Sztal, et al.
Nature Genetics|May 28, 2020
Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
Nature Genetics|May 6, 2020
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetesAndrea Cortese, Yi Zhu, Adriana P Rebelo, et al.
Pageof 13