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Massimo Acquaviva

Convergence between Microglia and Peripheral Macrophages Phenotype during Development and Neuroinflammation
2019 · Francesca Grassivaro, Ramesh Menon, et al. · Journal of Neuroscience · 132
Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies
2009 · Paola Mandich, Paola Fossa, et al. · European Journal of Human Genetics · 42
Inferring Multiple Sclerosis Stages from the Blood Transcriptome via Machine Learning
2020 · Massimo Acquaviva, Ramesh Menon, et al. · Cell Reports Medicine · 40
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Severe Neuropathy After Diphtheria-Tetanus-Pertussis Vaccination in a Child Carrying a Novel Frame-Shift Mutation in the Small Heat-Shock Protein 27 Gene
2009 · Paola Mandich, Marina Grandis, et al. · Journal of Child Neurology · 33
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Assessment of copy number variations in 120 patients with Poland syndrome
2016 · Carlotta Maria Vaccari, Elisa Tassano, et al. · BMC Medical Genetics · 31
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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
2020 · Federica Raggi, Davide Cangelosi, et al. · Journal of Translational Medicine · 20
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Design of a multi-signature ensemble classifier predicting neuroblastoma patients' outcome
2012 · Andrea Cornero, Massimo Acquaviva, et al. · BMC Bioinformatics · 20
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Machine learning-driven diagnosis of multiple sclerosis from whole blood transcriptomics
2024 · Maryam Omrani, Rosaria Rita Chiarelli, et al. · Brain Behavior and Immunity · 17
WES in a family trio suggests involvement of TECPR2 in a complex form of progressive motor neuron disease
2016 · A.E. Covone, C. Fiorillo, et al. · Clinical Genetics · 17
Loss of Circulating CD8+ CD161high T Cells in Primary Progressive Multiple Sclerosis
2019 · Massimo Acquaviva, Claudia Bassani, et al. · Frontiers in Immunology · 16
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Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease
2008 · Paola Mandich, Marina Grandis, et al. · Journal of Human Genetics · 16
Effects of heavy ions on visual function and electrophysiology of rodents: the ALTEA-MICE project
2004 · W.G. Sannita, M. Acquaviva, et al. · Advances in Space Research · 13
Identification of Multiple Hypoxia Signatures in Neuroblastoma Cell Lines by l1 - l2 Regularization and Data Reduction
2010 · Paolo Fardin, Andrea Cornero, et al. · BioMed Research International · 11
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MOESM4 of 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
2020 · Raggi, Federica, Cangelosi, Davide, et al. · Figshare
MOESM1 of 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
2020 · Raggi, Federica, Cangelosi, Davide, et al. · Figshare
MOESM3 of 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
2020 · Raggi, Federica, Cangelosi, Davide, et al. · Figshare
Additional file 2: of Assessment of copy number variations in 120 patients with Poland syndrome
2016 · Vaccari, Carlotta, Tassano, Elisa, et al. · Figshare
Additional file 1: of Assessment of copy number variations in 120 patients with Poland syndrome
2016 · Vaccari, Carlotta, Tassano, Elisa, et al. · Figshare
A new cross-platform multi-signature classifier approach to predict neuroblastoma patients outcome
2011 · Massimo Acquaviva, Andrea Cornero, et al. · F1000Research
Nanocomposite polymeric electrolytes to record electrophysiological brain signals in prolonged, unconventional or extreme conditions
2006 · Silvia Licoccia, M. Luisa Di Vona, et al. · Acta Biomaterialia
Sensorial and motor evaluation of dyslexia: preliminary report
1994 · Lorenzo Loffredo, Mario Cesarelli, et al.
Works count: 25
Citation count: 408
H-index: 12
I10-index: 13
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