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Molecular signaling and dysfunction of the human reactive enteric glial cell phenotype: implications for GI infection, IBD, POI, neurological, motility, and GI disorders
The complex molecular pharmacogenetics of wake promotion
Improvement of the Rett syndrome phenotype in a MeCP2 mouse model upon treatment with levodopa and a dopa-decarboxylase inhibitor
[PubMed] [Google Scholar] 45.Natali A., Santoro D., Brandi L.S., Faraggiana D., Ciociaro D., Pecori N., Buzzigoli G., Ferrannini E
