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Myoclonic dystonia

Known as: Hereditary essential myoclonus, MYOCLONUS-DYSTONIA SYNDROME, Myoclonus-Dystonia 
National Institutes of Health

Papers overview

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Review
2016
Review
2016
Dopamine transporter (DaT) single-photon emission computed tomography (SPECT) and [18F]fluoro-L-DOPA ([18F]DOPA) positron… 
2014
2014
We describe the case of a 42-year-old Japanese woman with childhood-onset myoclonus, dystonia, and psychiatric symptoms… 
Review
2013
Review
2013
Mutations in SGCE represent the major cause of the myoclonus‐dystonia syndrome (DYT11), an autosomal dominant disorder of reduced… 
2013
2013
Abstract Objective and importance: Myoclonus–dystonia syndrome (MDS, DYT11) is an inherited disorder characterized by clinical… 
2005
2005
This is a case study of a child who developed roseola infantum first, then varicella, and was later affected by acute cerebellar… 
2000
2000
ZusammenfassungGegenwärtig lassen sich 12 Typen von primären Dystonien (DYT1 – 12) genetisch unterscheiden. Die Deletion dreier… 
1999
1999
Therapy in hereditary essential myoclonus (HEM), a disabling movement disorder, is difficult in most cases, especially in regard… 
1985
1985
The use of a transcutaneous nerve stimulator yielded positive results in a condition marked by involuntary movements (tremors and…