Enrico Amico Centre for Neurogenetics and Rare Diseases IRCCS Neuromed Biography Publications Institution JoVE Articles Enrico Amico has not added a biography. If you are Enrico Amico and would like to personalize this page please email our Author Liaison for assistance. Publications Defective Sphingosine-1-phosphate Metabolism is a Druggable Target in Huntington's Disease Scientific Reports. Jul, 2017 | Pubmed ID: 28706199 Impairment of Blood-brain Barrier is an Early Event in R6/2 Mouse Model of Huntington Disease Scientific Reports. Jan, 2017 | Pubmed ID: 28117381 Impaired Levels of Gangliosides in the Corpus Callosum of Huntington Disease Animal Models Frontiers in Neuroscience. 2016 | Pubmed ID: 27766070 Terapeutic Potential of Microencapsulated Sertoli Cells in Huntington Disease CNS Neuroscience & Therapeutics. Aug, 2016 | Pubmed ID: 27225886 Pridopidine, a Dopamine Stabilizer, Improves Motor Performance and Shows Neuroprotective Effects in Huntington Disease R6/2 Mouse Model Journal of Cellular and Molecular Medicine. Nov, 2015 | Pubmed ID: 26094900 Nitric Oxide Dysregulation in Platelets from Patients with Advanced Huntington Disease PloS One. 2014 | Pubmed ID: 24587005 FTY720 (fingolimod) is a Neuroprotective and Disease-modifying Agent in Cellular and Mouse Models of Huntington Disease Human Molecular Genetics. May, 2014 | Pubmed ID: 24301680 Changes of Peripheral TGF-β1 Depend on Monocytes-derived Macrophages in Huntington Disease Molecular Brain. Dec, 2013 | Pubmed ID: 24330808 Early Defect of Transforming Growth Factor β1 Formation in Huntington's Disease Journal of Cellular and Molecular Medicine. Mar, 2011 | Pubmed ID: 20082658 神経変性疾患のマウスモデルで FITC 標識アルブミンの点滴静注による血液脳関門透過性の評価 Alba Di Pardo1, Salvatore Castaldo1, Luca Capocci1, Enrico Amico1, Vittorio Maglione1 1Centre for Neurogenetics and Rare Diseases, IRCCS Neuromed JoVE 56389 Neuroscience
神経変性疾患のマウスモデルで FITC 標識アルブミンの点滴静注による血液脳関門透過性の評価 Alba Di Pardo1, Salvatore Castaldo1, Luca Capocci1, Enrico Amico1, Vittorio Maglione1 1Centre for Neurogenetics and Rare Diseases, IRCCS Neuromed JoVE 56389 Neuroscience