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British Journal of Pharmacology
|
October 4, 2006
Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A-841720, a novel non-competitive mGluR1 receptor antagonist
O El-Kouhen, S G Lehto, J B Pan, et al.
Brain Communications
|
October 10, 2025
Biallelic <i>NDUFA9</i> variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency
Francesca Magrinelli, Lucie S Taylor, Sahar Sedighzadeh, et al.
The Lancet. Neurology
|
August 16, 2014
Pallidal neurostimulation in patients with medication-refractory cervical dystonia: a randomised, sham-controlled trial
Jens Volkmann, Joerg Mueller, Günther Deuschl, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 16, 2026
Biomarkers of Leucine-Rich Repeat Kinase 2 (LRRK2) and Lysosomal Dysfunction in Progressive Supranuclear Palsy
Louise-Kristine Nielsen, Joshua L I Frost, David P Vaughan, et al.
American Journal of Human Genetics
|
April 9, 2016
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions
Niccolò E Mencacci, Erik-Jan Kamsteeg, Kosuke Nakashima, et al.
The Journal of Clinical Investigation
|
February 4, 2021
Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia
Niccolò E Mencacci, Marisa M Brockmann, Jinye Dai, et al.
American Journal of Human Genetics
|
May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia
Niccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2025
Pathogenic variants in <i>BORCS5</i> Cause a Spectrum of Neurodevelopmental and Neurodegenerative Disorders with Lysosomal Dysfunction
Niccolò E Mencacci, Georgia Minakaki, Reza Maroofian, et al.
The Lancet. Neurology
|
June 20, 2025
Diagnostic and prognostic value of α-synuclein seed amplification assay kinetic measures in Parkinson's disease: a longitudinal cohort study
Christina D Orrú, David P Vaughan, Nirosen Vijiaratnam, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 19, 2019
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy
Max-Joseph Grimm, Gesine Respondek, Maria Stamelou, et al.
Page
of 80
Search research articles
Search
Showing results (771-780 of 797) with videos related to
Sort By:
Page
of 80
British Journal of Pharmacology
|
October 4, 2006
Blockade of mGluR1 receptor results in analgesia and disruption of motor and cognitive performances: effects of A-841720, a novel non-competitive mGluR1 receptor antagonist
O El-Kouhen, S G Lehto, J B Pan, et al.
Brain Communications
|
October 10, 2025
Biallelic <i>NDUFA9</i> variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency
Francesca Magrinelli, Lucie S Taylor, Sahar Sedighzadeh, et al.
The Lancet. Neurology
|
August 16, 2014
Pallidal neurostimulation in patients with medication-refractory cervical dystonia: a randomised, sham-controlled trial
Jens Volkmann, Joerg Mueller, Günther Deuschl, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 16, 2026
Biomarkers of Leucine-Rich Repeat Kinase 2 (LRRK2) and Lysosomal Dysfunction in Progressive Supranuclear Palsy
Louise-Kristine Nielsen, Joshua L I Frost, David P Vaughan, et al.
American Journal of Human Genetics
|
April 9, 2016
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions
Niccolò E Mencacci, Erik-Jan Kamsteeg, Kosuke Nakashima, et al.
The Journal of Clinical Investigation
|
February 4, 2021
Biallelic variants in TSPOAP1, encoding the active-zone protein RIMBP1, cause autosomal recessive dystonia
Niccolò E Mencacci, Marisa M Brockmann, Jinye Dai, et al.
American Journal of Human Genetics
|
May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia
Niccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 19, 2025
Pathogenic variants in <i>BORCS5</i> Cause a Spectrum of Neurodevelopmental and Neurodegenerative Disorders with Lysosomal Dysfunction
Niccolò E Mencacci, Georgia Minakaki, Reza Maroofian, et al.
The Lancet. Neurology
|
June 20, 2025
Diagnostic and prognostic value of α-synuclein seed amplification assay kinetic measures in Parkinson's disease: a longitudinal cohort study
Christina D Orrú, David P Vaughan, Nirosen Vijiaratnam, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 19, 2019
How to apply the movement disorder society criteria for diagnosis of progressive supranuclear palsy
Max-Joseph Grimm, Gesine Respondek, Maria Stamelou, et al.
Page
of 80