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Cecilia Marelli

Showing results (1-10 of 62) with videos related to

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Orphanet Journal of Rare Diseases|March 18, 2016
The P42 peptide and Peptide-based therapies for Huntington's diseaseCecilia Marelli, Florence Maschat
Journal of Neurology, Neurosurgery, and Psychiatry|August 29, 2018
Spinal cord involvement in adult-onset metabolic and genetic diseasesCecilia Marelli, Ettore Salsano, Letterio S Politi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Clinical and neuropsychological correlates in two brothers with pantothenate kinase-associated neurodegenerationCecilia Marelli, Sylvie Piacentini, Barbara Garavaglia, et al.
Molecular Genetics and Metabolism|February 13, 2025
The ELOVL proteins: Very and ultra long-chain fatty acids at the crossroads between metabolic and neurodegenerative disordersEnza Ferrero, Frédéric M Vaz, David Cheillan, et al.
JAMA Neurology|August 15, 2022
Adult-Onset Genetic Central Nervous System Disorders Masquerading as Acquired Neuroinflammatory Disorders: A ReviewXavier Ayrignac, Clarisse Carra-Dallière, Cecilia Marelli, et al.
Archives of Neurology|March 7, 2012
A serine synthesis defect presenting with a Charcot-Marie-Tooth-like polyneuropathyAurélie Méneret, Elsa Wiame, Cecilia Marelli, et al.
Journal of Alzheimer'S Disease : JAD|January 13, 2016
Limiting Factors of Brain Donation in Neurodegenerative Diseases: The Example of French Memory ClinicsRaphael Le Bouc, Cecilia Marelli, Emilie Beaufils, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2008
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndromeGiacomina Rossi, Cecilia Marelli, Laura Farina, et al.
Neurology. Genetics|June 15, 2026
Blood Neurofilament Light Chain and Glial Fibrillary Acidic Protein as Candidate Biomarkers in <i>CSF1R</i>-Related DisorderXavier Ayrignac, Cecilia Marelli, Sylvain Lehmann, et al.
Movement Disorders Clinical Practice|February 5, 2019
Cerebral Iron Accumulation Is Not a Major Feature of <i>FA2H</i>/SPG35Cecilia Marelli, Mustafa A Salih, Karine Nguyen, et al.
Pageof 7

Showing results (1-10 of 62) with videos related to

Sort By:
Pageof 7
Orphanet Journal of Rare Diseases|March 18, 2016
The P42 peptide and Peptide-based therapies for Huntington's diseaseCecilia Marelli, Florence Maschat
Journal of Neurology, Neurosurgery, and Psychiatry|August 29, 2018
Spinal cord involvement in adult-onset metabolic and genetic diseasesCecilia Marelli, Ettore Salsano, Letterio S Politi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Clinical and neuropsychological correlates in two brothers with pantothenate kinase-associated neurodegenerationCecilia Marelli, Sylvie Piacentini, Barbara Garavaglia, et al.
Molecular Genetics and Metabolism|February 13, 2025
The ELOVL proteins: Very and ultra long-chain fatty acids at the crossroads between metabolic and neurodegenerative disordersEnza Ferrero, Frédéric M Vaz, David Cheillan, et al.
JAMA Neurology|August 15, 2022
Adult-Onset Genetic Central Nervous System Disorders Masquerading as Acquired Neuroinflammatory Disorders: A ReviewXavier Ayrignac, Clarisse Carra-Dallière, Cecilia Marelli, et al.
Archives of Neurology|March 7, 2012
A serine synthesis defect presenting with a Charcot-Marie-Tooth-like polyneuropathyAurélie Méneret, Elsa Wiame, Cecilia Marelli, et al.
Journal of Alzheimer'S Disease : JAD|January 13, 2016
Limiting Factors of Brain Donation in Neurodegenerative Diseases: The Example of French Memory ClinicsRaphael Le Bouc, Cecilia Marelli, Emilie Beaufils, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 1, 2008
The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndromeGiacomina Rossi, Cecilia Marelli, Laura Farina, et al.
Neurology. Genetics|June 15, 2026
Blood Neurofilament Light Chain and Glial Fibrillary Acidic Protein as Candidate Biomarkers in <i>CSF1R</i>-Related DisorderXavier Ayrignac, Cecilia Marelli, Sylvain Lehmann, et al.
Movement Disorders Clinical Practice|February 5, 2019
Cerebral Iron Accumulation Is Not a Major Feature of <i>FA2H</i>/SPG35Cecilia Marelli, Mustafa A Salih, Karine Nguyen, et al.
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