Repetitive transcranial magnetic stimulation alleviates motor impairment in Parkinson’s disease: association with peripheral inflammatory regulatory T-cells and SYT6

Repetitive transcranial magnetic stimulation (rTMS) has been used to treat various neurological disorders. However, the molecular mechanism underlying the therapeutic effect of rTMS on Parkinson’s disease (PD)…

Brain pathways that control dopamine release may influence motor control

Within the human brain, movement is coordinated by a brain region called the striatum, which sends instructions to motor neurons in the brain. Those instructions are conveyed by two pathways, one that initiates movement (“go”) and one that suppresses it (“no-go”). In a new study, MIT researchers have discovered an additional two pathways that arise… Continue reading Brain pathways that control dopamine release may influence motor control

Brain pathways that control dopamine release may influence motor control

Within the human brain, movement is coordinated by a brain region called the striatum, which sends instructions to motor neurons in the brain. Those instructions are conveyed by two pathways, one that initiates movement (“go”) and one that suppresses it (“no-go”). In a new study, MIT researchers have discovered an additional two pathways that arise… Continue reading Brain pathways that control dopamine release may influence motor control

Brain pathways that control dopamine release may influence motor control

Within the human brain, movement is coordinated by a brain region called the striatum, which sends instructions to motor neurons in the brain. Those instructions are conveyed by two pathways, one that initiates movement (“go”) and one that suppresses it (“no-go”). In a new study, MIT researchers have discovered an additional two pathways that arise… Continue reading Brain pathways that control dopamine release may influence motor control

[Comment] The global dimension of Parkinson’s disease genetics

Since 1997, with the discovery of the Parkinson’s disease-causing Ala53Thr variant in SNCA, the gene that encodes α-synuclein,1 our understanding of this common neurodegenerative disease has fundamentally changed, mainly due to a large number of genetic discoveries over the past 25 years. This journey is extensively and elegantly summarised by Shen-Yang Lim and colleagues in… Continue reading [Comment] The global dimension of Parkinson’s disease genetics