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Maria E Rubio

Showing results (31-40 of 35) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 13, 2015
Loss of VGLUT3 Produces Circadian-Dependent Hyperdopaminergia and Ameliorates Motor Dysfunction and l-Dopa-Mediated Dyskinesias in a Model of Parkinson's DiseaseChristopher B Divito, Kathy Steece-Collier, Daniel T Case, et al.
Cell Reports|March 21, 2024
Long-range inhibitory neurons mediate cortical neurovascular couplingCatherine F Ruff, Fernanda Juarez Anaya, Samuel J Dienel, et al.
Science (New York, N.Y.)|July 7, 2012
Bergmann glial AMPA receptors are required for fine motor coordinationAiman S Saab, Alexander Neumeyer, Hannah M Jahn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patientsRudy G E van Eijsden, Mike Gerards, Lars M T Eijssen, et al.
Journal of Inherited Metabolic Disease|March 1, 2019
Movement disorders and nonmotor neuropsychological symptoms in children and adults with classical galactosemiaAnouk Kuiper, Stephanie Grünewald, Elaine Murphy, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 13, 2015
Loss of VGLUT3 Produces Circadian-Dependent Hyperdopaminergia and Ameliorates Motor Dysfunction and l-Dopa-Mediated Dyskinesias in a Model of Parkinson's DiseaseChristopher B Divito, Kathy Steece-Collier, Daniel T Case, et al.
Cell Reports|March 21, 2024
Long-range inhibitory neurons mediate cortical neurovascular couplingCatherine F Ruff, Fernanda Juarez Anaya, Samuel J Dienel, et al.
Science (New York, N.Y.)|July 7, 2012
Bergmann glial AMPA receptors are required for fine motor coordinationAiman S Saab, Alexander Neumeyer, Hannah M Jahn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Chip-based mtDNA mutation screening enables fast and reliable genetic diagnosis of OXPHOS patientsRudy G E van Eijsden, Mike Gerards, Lars M T Eijssen, et al.
Journal of Inherited Metabolic Disease|March 1, 2019
Movement disorders and nonmotor neuropsychological symptoms in children and adults with classical galactosemiaAnouk Kuiper, Stephanie Grünewald, Elaine Murphy, et al.
Pageof 4