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Science Translational Medicine
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April 2, 2025
Mavoglurant reduces cocaine use in patients with cocaine use disorder in a phase 2 clinical trial
Baltazar Gomez-Mancilla, Kenneth M Dürsteler, Marc Vogel, et al.
Cell Reports
|
June 1, 2022
Sustained Trem2 stabilization accelerates microglia heterogeneity and Aβ pathology in a mouse model of Alzheimer's disease
Rahul Dhandapani, Marilisa Neri, Mario Bernhard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 13, 2011
AFQ056 treatment of levodopa-induced dyskinesias: results of 2 randomized controlled trials
Daniela Berg, Jana Godau, Claudia Trenkwalder, et al.
Nature Reviews. Drug Discovery
|
December 9, 2017
Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome
Elizabeth M Berry-Kravis, Lothar Lindemann, Aia E Jønch, et al.
Science Translational Medicine
|
January 7, 2011
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056
Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 65) with videos related to
Sort By:
Page
of 7
You have reached the last page of results.
This site can display upto 65 results.
Science Translational Medicine
|
April 2, 2025
Mavoglurant reduces cocaine use in patients with cocaine use disorder in a phase 2 clinical trial
Baltazar Gomez-Mancilla, Kenneth M Dürsteler, Marc Vogel, et al.
Cell Reports
|
June 1, 2022
Sustained Trem2 stabilization accelerates microglia heterogeneity and Aβ pathology in a mouse model of Alzheimer's disease
Rahul Dhandapani, Marilisa Neri, Mario Bernhard, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 13, 2011
AFQ056 treatment of levodopa-induced dyskinesias: results of 2 randomized controlled trials
Daniela Berg, Jana Godau, Claudia Trenkwalder, et al.
Nature Reviews. Drug Discovery
|
December 9, 2017
Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome
Elizabeth M Berry-Kravis, Lothar Lindemann, Aia E Jønch, et al.
Science Translational Medicine
|
January 7, 2011
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056
Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
Page
of 7