Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia
A Sperandeo, C Tamburini, Z Noakes, DC de la Fuente… - Brain, 2023 - academic.oup.com
Myoclonus dystonia is a childhood-onset hyperkinetic movement disorder with a combined
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia
A Sperandeo, C Tamburini… - Brain: a journal of …, 2023 - pubmed.ncbi.nlm.nih.gov
Myoclonus dystonia is a childhood-onset hyperkinetic movement disorder with a combined
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
[HTML][HTML] Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia
A Sperandeo, C Tamburini, Z Noakes, DC de la Fuente… - Brain, 2023 - ncbi.nlm.nih.gov
Myoclonus dystonia is a childhood-onset hyperkinetic movement disorder with a combined
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia.
A Sperandeo, C Tamburini, Z Noakes… - Brain: A Journal of …, 2023 - search.ebscohost.com
Myoclonus dystonia is a childhood-onset hyperkinetic movement disorder with a combined
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
[PDF][PDF] Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia
A Sperandeo, C Tamburini, Z Noakes… - …, 2023 - pdfs.semanticscholar.org
Dystonia is one of the most common forms of movement disorder, with an estimated
population prevalence of 1.2%. 1 It involves loss of coordinated contraction of antagonistic …
population prevalence of 1.2%. 1 It involves loss of coordinated contraction of antagonistic …
[PDF][PDF] Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia
A Sperandeo, C Tamburini, Z Noakes, DC de la Fuente… - Brain, 2023 - academic.oup.com
Myoclonus dystonia is a childhood-onset hyperkinetic movement disorder with a combined
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia.
A Sperandeo, C Tamburini, Z Noakes… - Brain: a Journal of …, 2023 - europepmc.org
Myoclonus dystonia is a childhood-onset hyperkinetic movement disorder with a combined
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia
A Sperandeo, C Tamburini, Z Noakes… - Brain, 2023 - orca.cardiff.ac.uk
Myoclonus Dystonia is a childhood-onset hyperkinetic movement disorder with a combined
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia.
A Sperandeo, C Tamburini, Z Noakes… - Brain: a Journal of …, 2022 - europepmc.org
Myoclonus Dystonia is a childhood-onset hyperkinetic movement disorder with a combined
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …
motor and psychiatric phenotype. It represents one of the few autosomal dominant inherited …