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Brain : a Journal of Neurology
|
September 3, 2004
Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines
Simone Beretta, Laura Mattavelli, Gessica Sala, et al.
Disability and Rehabilitation
|
December 9, 2009
The dystonic child treated with deep brain stimulation: ICF reading of a high-tech approach
Elisa Petacchi, Maria Teresa Armellin, Dina Facchin, et al.
Disability and Rehabilitation
|
December 9, 2009
The ICF and labour policies project: the first Italian nation-wide experience of ICF implementation in the Labour Sector
Mario Conclave, Guido Fusaro, Marina Sala, et al.
Frontiers in Neurology
|
August 9, 2020
Brain Magnetic Spectroscopy Imaging and Hereditary Spastic Paraplegia: A Focused Systematic Review on Current Landmarks and Future Perspectives
Marinela Vavla, Domenico Montanaro, Silvia Pizzighello, et al.
Child and Adolescent Psychiatry and Mental Health
|
February 16, 2023
The perceived impact of Covid-19 pandemic on the children with cerebral palsy: the parents' perspective explored within the "6-F words" framework
Silvia Pizzighello, Marianna Uliana, Michela Martinuzzi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 10, 2008
The first Italian family with evidence of pyramidal impairment as phenotypic manifestation of Silver syndrome BSCL2 gene mutation
Gianfranco Cafforio, Rosanna Calabrese, Nicola Morelli, et al.
The Journal of Biological Chemistry
|
December 3, 2008
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels
Anna Maria Porcelli, Alessia Angelin, Anna Ghelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 22, 2025
STOP-HSP.net: An Italian formal registry for clinical trial readiness in hereditary spastic paraplegias
Sara Satolli, Salvatore Rossi, Leonardo Boccuni, et al.
Brain : a Journal of Neurology
|
February 25, 2005
Isolation of transcriptomal changes attributable to LHON mutations and the cybridization process
Steven R Danielson, Valerio Carelli, Guolin Tan, et al.
Journal of Neuroscience Research
|
July 11, 2008
Antioxidants partially restore glutamate transport defect in leber hereditary optic neuropathy cybrids
Gessica Sala, Federica Trombin, Simone Beretta, et al.
Page
of 17
Search research articles
Search
Showing results (71-80 of 163) with videos related to
Sort By:
Page
of 17
Brain : a Journal of Neurology
|
September 3, 2004
Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines
Simone Beretta, Laura Mattavelli, Gessica Sala, et al.
Disability and Rehabilitation
|
December 9, 2009
The dystonic child treated with deep brain stimulation: ICF reading of a high-tech approach
Elisa Petacchi, Maria Teresa Armellin, Dina Facchin, et al.
Disability and Rehabilitation
|
December 9, 2009
The ICF and labour policies project: the first Italian nation-wide experience of ICF implementation in the Labour Sector
Mario Conclave, Guido Fusaro, Marina Sala, et al.
Frontiers in Neurology
|
August 9, 2020
Brain Magnetic Spectroscopy Imaging and Hereditary Spastic Paraplegia: A Focused Systematic Review on Current Landmarks and Future Perspectives
Marinela Vavla, Domenico Montanaro, Silvia Pizzighello, et al.
Child and Adolescent Psychiatry and Mental Health
|
February 16, 2023
The perceived impact of Covid-19 pandemic on the children with cerebral palsy: the parents' perspective explored within the "6-F words" framework
Silvia Pizzighello, Marianna Uliana, Michela Martinuzzi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 10, 2008
The first Italian family with evidence of pyramidal impairment as phenotypic manifestation of Silver syndrome BSCL2 gene mutation
Gianfranco Cafforio, Rosanna Calabrese, Nicola Morelli, et al.
The Journal of Biological Chemistry
|
December 3, 2008
Respiratory complex I dysfunction due to mitochondrial DNA mutations shifts the voltage threshold for opening of the permeability transition pore toward resting levels
Anna Maria Porcelli, Alessia Angelin, Anna Ghelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
February 22, 2025
STOP-HSP.net: An Italian formal registry for clinical trial readiness in hereditary spastic paraplegias
Sara Satolli, Salvatore Rossi, Leonardo Boccuni, et al.
Brain : a Journal of Neurology
|
February 25, 2005
Isolation of transcriptomal changes attributable to LHON mutations and the cybridization process
Steven R Danielson, Valerio Carelli, Guolin Tan, et al.
Journal of Neuroscience Research
|
July 11, 2008
Antioxidants partially restore glutamate transport defect in leber hereditary optic neuropathy cybrids
Gessica Sala, Federica Trombin, Simone Beretta, et al.
Page
of 17