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Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
December 13, 2025
Low-dose combination of ultramicronized palmitoylethanolamide and docosahexaenoic acid on neurosteroid and neuroinflammatory dysregulation in autism spectrum disorders
Fabiana Filogamo, Fabrizio Maria Liguori, Giovanna La Rana, et al.
Biomolecules
|
August 26, 2022
The Beneficial Effects of Ultramicronized Palmitoylethanolamide in the Management of Neuropathic Pain and Associated Mood Disorders Induced by Paclitaxel in Mice
Claudia Cristiano, Carmen Avagliano, Mariarosaria Cuozzo, et al.
Neuroreport
|
February 22, 2008
Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume
Antonio Cerasa, Maria C Gioia, Angelo Labate, et al.
International Journal of Molecular Sciences
|
November 23, 2018
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis
Nicoletta Nuzziello, Laura Vilardo, Paride Pelucchi, et al.
Brain Sciences
|
June 26, 2026
Longitudinal Transcriptomic Analysis Reveals Systemic Effects of Risdiplam in Adults with Spinal Muscular Atrophy
Maria Liguori, Arianna Consiglio, Eustachio D'Errico, et al.
Plos One
|
August 8, 2014
Proteomic profiling in multiple sclerosis clinical courses reveals potential biomarkers of neurodegeneration
Maria Liguori, Antonio Qualtieri, Carla Tortorella, et al.
Brain and Cognition
|
August 25, 2009
Neurofunctional correlates of personality traits in relapsing-remitting multiple sclerosis: an fMRI study
Maria C Gioia, Antonio Cerasa, Paola Valentino, et al.
Brain : a Journal of Neurology
|
May 8, 2009
Neurobiological mechanisms underlying emotional processing in relapsing-remitting multiple sclerosis
Luca Passamonti, Antonio Cerasa, Maria Liguori, et al.
Journal of Neurology
|
January 22, 2008
A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation
Maria Liguori, Antonella La Russa, Ida Manna, et al.
Human Genetics
|
October 21, 2010
Gene symbol: NOTCH3. Disease: CADASIL
Carmine Ungaro, Teresa Sprovieri, Francesca Luisa Conforti, et al.
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Search research articles
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Showing results (11-20 of 66) with videos related to
Sort By:
Page
of 7
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
December 13, 2025
Low-dose combination of ultramicronized palmitoylethanolamide and docosahexaenoic acid on neurosteroid and neuroinflammatory dysregulation in autism spectrum disorders
Fabiana Filogamo, Fabrizio Maria Liguori, Giovanna La Rana, et al.
Biomolecules
|
August 26, 2022
The Beneficial Effects of Ultramicronized Palmitoylethanolamide in the Management of Neuropathic Pain and Associated Mood Disorders Induced by Paclitaxel in Mice
Claudia Cristiano, Carmen Avagliano, Mariarosaria Cuozzo, et al.
Neuroreport
|
February 22, 2008
Impact of catechol-O-methyltransferase Val(108/158) Met genotype on hippocampal and prefrontal gray matter volume
Antonio Cerasa, Maria C Gioia, Angelo Labate, et al.
International Journal of Molecular Sciences
|
November 23, 2018
Investigating the Role of MicroRNA and Transcription Factor Co-regulatory Networks in Multiple Sclerosis Pathogenesis
Nicoletta Nuzziello, Laura Vilardo, Paride Pelucchi, et al.
Brain Sciences
|
June 26, 2026
Longitudinal Transcriptomic Analysis Reveals Systemic Effects of Risdiplam in Adults with Spinal Muscular Atrophy
Maria Liguori, Arianna Consiglio, Eustachio D'Errico, et al.
Plos One
|
August 8, 2014
Proteomic profiling in multiple sclerosis clinical courses reveals potential biomarkers of neurodegeneration
Maria Liguori, Antonio Qualtieri, Carla Tortorella, et al.
Brain and Cognition
|
August 25, 2009
Neurofunctional correlates of personality traits in relapsing-remitting multiple sclerosis: an fMRI study
Maria C Gioia, Antonio Cerasa, Paola Valentino, et al.
Brain : a Journal of Neurology
|
May 8, 2009
Neurobiological mechanisms underlying emotional processing in relapsing-remitting multiple sclerosis
Luca Passamonti, Antonio Cerasa, Maria Liguori, et al.
Journal of Neurology
|
January 22, 2008
A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation
Maria Liguori, Antonella La Russa, Ida Manna, et al.
Human Genetics
|
October 21, 2010
Gene symbol: NOTCH3. Disease: CADASIL
Carmine Ungaro, Teresa Sprovieri, Francesca Luisa Conforti, et al.
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of 7