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Christian Lunetta

Showing results (101-110 of 167) with videos related to

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Journal of Alternative and Complementary Medicine (New York, N.Y.)|December 17, 2013
Meditation training for people with amyotrophic lateral sclerosis and their caregiversFrancesco Pagnini, Chiara Di Credico, Ramona Gatto, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 31, 2019
HSC70 expression is reduced in lymphomonocytes of sporadic ALS patients and contributes to TDP-43 accumulationAlessandro Arosio, Riccardo Cristofani, Orietta Pansarasa, et al.
The Open Neurology Journal|September 22, 2016
Osteopathic Manual Treatment for Amyotrophic Lateral Sclerosis: A Feasibility Pilot StudyAlberto Maggiani, Lucio Tremolizzo, Andrea Della Valentina, et al.
Journal of Neurology|March 10, 2022
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progressionErica Tavazzi, Sebastian Daberdaku, Alessandro Zandonà, et al.
Neurobiology of Aging|April 13, 2010
Lack of association of PON polymorphisms with sporadic ALS in an Italian populationClaudia Ricci, Stefania Battistini, Lorena Cozzi, et al.
Neurology|September 10, 2021
Association of Clinically Evident Eye Movement Abnormalities With Motor and Cognitive Features in Patients With Motor Neuron DisordersBarbara Poletti, Federica Solca, Laura Carelli, et al.
Frontiers in Molecular Neuroscience|April 22, 2017
Decreased Levels of Foldase and Chaperone Proteins Are Associated with an Early-Onset Amyotrophic Lateral SclerosisMelania Filareti, Silvia Luotti, Laura Pasetto, et al.
Neurobiology of Aging|April 20, 2019
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALSSerena Lattante, Paolo Niccolò Doronzio, Giuseppe Marangi, et al.
Neurobiology of Aging|February 27, 2021
The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairmentPaola Lanteri, Irene Meola, Antonio Canosa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 7, 2019
ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usabilityLucio Tremolizzo, Andrea Lizio, Gabriella Santangelo, et al.
Pageof 17

Showing results (101-110 of 167) with videos related to

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Pageof 17
Journal of Alternative and Complementary Medicine (New York, N.Y.)|December 17, 2013
Meditation training for people with amyotrophic lateral sclerosis and their caregiversFrancesco Pagnini, Chiara Di Credico, Ramona Gatto, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 31, 2019
HSC70 expression is reduced in lymphomonocytes of sporadic ALS patients and contributes to TDP-43 accumulationAlessandro Arosio, Riccardo Cristofani, Orietta Pansarasa, et al.
The Open Neurology Journal|September 22, 2016
Osteopathic Manual Treatment for Amyotrophic Lateral Sclerosis: A Feasibility Pilot StudyAlberto Maggiani, Lucio Tremolizzo, Andrea Della Valentina, et al.
Journal of Neurology|March 10, 2022
Predicting functional impairment trajectories in amyotrophic lateral sclerosis: a probabilistic, multifactorial model of disease progressionErica Tavazzi, Sebastian Daberdaku, Alessandro Zandonà, et al.
Neurobiology of Aging|April 13, 2010
Lack of association of PON polymorphisms with sporadic ALS in an Italian populationClaudia Ricci, Stefania Battistini, Lorena Cozzi, et al.
Neurology|September 10, 2021
Association of Clinically Evident Eye Movement Abnormalities With Motor and Cognitive Features in Patients With Motor Neuron DisordersBarbara Poletti, Federica Solca, Laura Carelli, et al.
Frontiers in Molecular Neuroscience|April 22, 2017
Decreased Levels of Foldase and Chaperone Proteins Are Associated with an Early-Onset Amyotrophic Lateral SclerosisMelania Filareti, Silvia Luotti, Laura Pasetto, et al.
Neurobiology of Aging|April 20, 2019
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALSSerena Lattante, Paolo Niccolò Doronzio, Giuseppe Marangi, et al.
Neurobiology of Aging|February 27, 2021
The heterozygous deletion c.1509_1510delAG in exon 14 of FUS causes an aggressive childhood-onset ALS with cognitive impairmentPaola Lanteri, Irene Meola, Antonio Canosa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 7, 2019
ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usabilityLucio Tremolizzo, Andrea Lizio, Gabriella Santangelo, et al.
Pageof 17