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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 disease
Paola 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 reduction
Paolo 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 Neuroinflammation
Francesca 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 neuropathies
Paola Mandich, Paola Fossa, Simona Capponi, et al.
BMC Bioinformatics
|
April 28, 2012
Design of a multi-signature ensemble classifier predicting neuroblastoma patients' outcome
Andrea 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 Sclerosis
Massimo Acquaviva, Claudia Bassani, Nicole Sarno, et al.
Cell Reports. Medicine
|
November 18, 2020
Inferring Multiple Sclerosis Stages from the Blood Transcriptome via Machine Learning
Massimo 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 conditions
Silvia 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 bypass
Federica 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 gene
Paola Mandich, Marina Grandis, Alessandra Varese, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Journal of Human Genetics
|
April 2, 2008
Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease
Paola 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 reduction
Paolo 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 Neuroinflammation
Francesca 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 neuropathies
Paola Mandich, Paola Fossa, Simona Capponi, et al.
BMC Bioinformatics
|
April 28, 2012
Design of a multi-signature ensemble classifier predicting neuroblastoma patients' outcome
Andrea 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 Sclerosis
Massimo Acquaviva, Claudia Bassani, Nicole Sarno, et al.
Cell Reports. Medicine
|
November 18, 2020
Inferring Multiple Sclerosis Stages from the Blood Transcriptome via Machine Learning
Massimo 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 conditions
Silvia 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 bypass
Federica 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 gene
Paola Mandich, Marina Grandis, Alessandra Varese, et al.
Page
of 2