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Frontiers in Genetics
|
December 15, 2023
Prominent muscle involvement in a familial form of mitochondrial disease due to a <i>COA8</i> variant
Martina Rimoldi, Francesca Magri, Sara Antognozzi, et al.
Frontiers in Neurology
|
March 19, 2024
Case report: A novel <i>ACTA1</i> variant in a patient with nemaline rods and increased glycogen deposition
Daniela Piga, Martina Rimoldi, Francesca Magri, et al.
Frontiers in Psychology
|
May 1, 2015
Managing chronic pathologies with a stepped mHealth-based approach in clinical psychology and medicine
Gianluca Castelnuovo, Italo Zoppis, Eugenio Santoro, et al.
Annals of Clinical and Translational Neurology
|
April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency
Dario Ronchi, Edoardo Monfrini, Sara Bonato, et al.
Scientific Reports
|
April 14, 2022
Clinical and genetic features of a cohort of patients with MFN2-related neuropathy
Elena Abati, Arianna Manini, Daniele Velardo, et al.
Cells
|
July 6, 2023
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in <i>Phospholamban</i> Gene
Simona Zanotti, Michela Ripolone, Laura Napoli, et al.
BMC Neurology
|
January 18, 2013
POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndrome
Antonella Cheldi, Dario Ronchi, Andreina Bordoni, et al.
Journal of the Neurological Sciences
|
November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction
Stefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Ageing Research Reviews
|
November 16, 2023
Genomic and transcriptomic advances in amyotrophic lateral sclerosis
Mafalda Rizzuti, Luca Sali, Valentina Melzi, et al.
Brain Sciences
|
December 23, 2023
Lafora Disease: A Case Report and Evolving Treatment Advancements
Carola Rita Ferrari Aggradi, Martina Rimoldi, Gloria Romagnoli, et al.
Page
of 29
Search research articles
Search
Showing results (191-200 of 287) with videos related to
Sort By:
Page
of 29
Frontiers in Genetics
|
December 15, 2023
Prominent muscle involvement in a familial form of mitochondrial disease due to a <i>COA8</i> variant
Martina Rimoldi, Francesca Magri, Sara Antognozzi, et al.
Frontiers in Neurology
|
March 19, 2024
Case report: A novel <i>ACTA1</i> variant in a patient with nemaline rods and increased glycogen deposition
Daniela Piga, Martina Rimoldi, Francesca Magri, et al.
Frontiers in Psychology
|
May 1, 2015
Managing chronic pathologies with a stepped mHealth-based approach in clinical psychology and medicine
Gianluca Castelnuovo, Italo Zoppis, Eugenio Santoro, et al.
Annals of Clinical and Translational Neurology
|
April 25, 2020
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency
Dario Ronchi, Edoardo Monfrini, Sara Bonato, et al.
Scientific Reports
|
April 14, 2022
Clinical and genetic features of a cohort of patients with MFN2-related neuropathy
Elena Abati, Arianna Manini, Daniele Velardo, et al.
Cells
|
July 6, 2023
Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in <i>Phospholamban</i> Gene
Simona Zanotti, Michela Ripolone, Laura Napoli, et al.
BMC Neurology
|
January 18, 2013
POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndrome
Antonella Cheldi, Dario Ronchi, Andreina Bordoni, et al.
Journal of the Neurological Sciences
|
November 13, 2008
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction
Stefania Corti, Chiara Donadoni, Dario Ronchi, et al.
Ageing Research Reviews
|
November 16, 2023
Genomic and transcriptomic advances in amyotrophic lateral sclerosis
Mafalda Rizzuti, Luca Sali, Valentina Melzi, et al.
Brain Sciences
|
December 23, 2023
Lafora Disease: A Case Report and Evolving Treatment Advancements
Carola Rita Ferrari Aggradi, Martina Rimoldi, Gloria Romagnoli, et al.
Page
of 29