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Centre for Neurogenetics and Rare Diseases
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Early defect of transforming growth factor β1 formation in Huntington's disease.
Journal of cellular and molecular medicine Mar, 2011 | Pubmed ID: 20082658
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
Nitric oxide dysregulation in platelets from patients with advanced Huntington disease.
PloS one , 2014 | Pubmed ID: 24587005
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
Terapeutic Potential of Microencapsulated Sertoli Cells in Huntington Disease.
CNS neuroscience & therapeutics Aug, 2016 | Pubmed ID: 27225886
Impaired Levels of Gangliosides in the Corpus Callosum of Huntington Disease Animal Models.
Frontiers in neuroscience , 2016 | Pubmed ID: 27766070
Impairment of blood-brain barrier is an early event in R6/2 mouse model of Huntington Disease.
Scientific reports Jan, 2017 | Pubmed ID: 28117381
Defective Sphingosine-1-phosphate metabolism is a druggable target in Huntington's disease.
Scientific reports Jul, 2017 | Pubmed ID: 28706199
IRCCS Neuromed
Alba Di Pardo1,
Salvatore Castaldo1,
Luca Capocci1,
Enrico Amico1,
Vittorio Maglione1
1Centre for Neurogenetics and Rare Diseases, IRCCS Neuromed
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