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Massimo Acquaviva

Showing results (1-10 of 12) with videos related to

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Journal of Human Genetics|April 2, 2008
Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth diseasePaola Mandich, Marina Grandis, Alessandro Geroldi, et al.
Journal of Biomedicine & Biotechnology|July 24, 2010
Identification of multiple hypoxia signatures in neuroblastoma cell lines by l1-l2 regularization and data reductionPaolo Fardin, Andrea Cornero, Annalisa Barla, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 11, 2019
Convergence between Microglia and Peripheral Macrophages Phenotype during Development and NeuroinflammationFrancesca Grassivaro, Ramesh Menon, Massimo Acquaviva, et al.
European Journal of Human Genetics : EJHG|March 19, 2009
Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathiesPaola Mandich, Paola Fossa, Simona Capponi, et al.
BMC Bioinformatics|April 28, 2012
Design of a multi-signature ensemble classifier predicting neuroblastoma patients' outcomeAndrea Cornero, Massimo Acquaviva, Paolo Fardin, et al.
Frontiers in Immunology|September 3, 2019
Loss of Circulating CD8+ CD161<sup>high</sup> T Cells in Primary Progressive Multiple SclerosisMassimo Acquaviva, Claudia Bassani, Nicole Sarno, et al.
Cell Reports. Medicine|November 18, 2020
Inferring Multiple Sclerosis Stages from the Blood Transcriptome via Machine LearningMassimo Acquaviva, Ramesh Menon, Marco Di Dario, et al.
Acta Biomaterialia|July 15, 2006
Nanocomposite polymeric electrolytes to record electrophysiological brain signals in prolonged, unconventional or extreme conditionsSilvia Licoccia, M Luisa Di Vona, Paola Romagnoli, et al.
Journal of Translational Medicine|January 12, 2020
Transcriptome analysis defines myocardium gene signatures in children with ToF and ASD and reveals disease-specific molecular reprogramming in response to surgery with cardiopulmonary bypassFederica Raggi, Davide Cangelosi, Pamela Becherini, et al.
Journal of Child Neurology|May 14, 2009
Severe neuropathy after diphtheria-tetanus-pertussis vaccination in a child carrying a novel frame-shift mutation in the small heat-shock protein 27 genePaola Mandich, Marina Grandis, Alessandra Varese, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Human Genetics|April 2, 2008
Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth diseasePaola Mandich, Marina Grandis, Alessandro Geroldi, et al.
Journal of Biomedicine & Biotechnology|July 24, 2010
Identification of multiple hypoxia signatures in neuroblastoma cell lines by l1-l2 regularization and data reductionPaolo Fardin, Andrea Cornero, Annalisa Barla, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 11, 2019
Convergence between Microglia and Peripheral Macrophages Phenotype during Development and NeuroinflammationFrancesca Grassivaro, Ramesh Menon, Massimo Acquaviva, et al.
European Journal of Human Genetics : EJHG|March 19, 2009
Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathiesPaola Mandich, Paola Fossa, Simona Capponi, et al.
BMC Bioinformatics|April 28, 2012
Design of a multi-signature ensemble classifier predicting neuroblastoma patients' outcomeAndrea Cornero, Massimo Acquaviva, Paolo Fardin, et al.
Frontiers in Immunology|September 3, 2019
Loss of Circulating CD8+ CD161<sup>high</sup> T Cells in Primary Progressive Multiple SclerosisMassimo Acquaviva, Claudia Bassani, Nicole Sarno, et al.
Cell Reports. Medicine|November 18, 2020
Inferring Multiple Sclerosis Stages from the Blood Transcriptome via Machine LearningMassimo Acquaviva, Ramesh Menon, Marco Di Dario, et al.
Acta Biomaterialia|July 15, 2006
Nanocomposite polymeric electrolytes to record electrophysiological brain signals in prolonged, unconventional or extreme conditionsSilvia Licoccia, M Luisa Di Vona, Paola Romagnoli, et al.
Journal of Translational Medicine|January 12, 2020
Transcriptome analysis defines myocardium gene signatures in children with ToF and ASD and reveals disease-specific molecular reprogramming in response to surgery with cardiopulmonary bypassFederica Raggi, Davide Cangelosi, Pamela Becherini, et al.
Journal of Child Neurology|May 14, 2009
Severe neuropathy after diphtheria-tetanus-pertussis vaccination in a child carrying a novel frame-shift mutation in the small heat-shock protein 27 genePaola Mandich, Marina Grandis, Alessandra Varese, et al.
Pageof 2