Physiological investigations continue to define the processes underlying different types of myoclonus, particularly cortical forms. Several new aetiologies have been described and genetic advances have revealed the basic deficit in familial hyperekplexia
A clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy b
The term "myoclonus " sounds esoteric, yet it is part of our normal physiology, occurring ...
Background: Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characteri...
Physiological investigations continue to define the processes underlying different types of myoclonu...
This review examines some of the advances in understanding myoclonus over the last 25 years. The cla...
Few movement disorders seem to make a straightforward approach to diagnosis and treatment more diffi...
Genetically determined myoclonus disorders are a result of a large number of genes. They have wide c...
Myoclonus is a hyperkinetic movement disorder characterized by brief, involuntary muscular jerks. Re...
peer reviewedCan a gene defect be responsible for the occurrence in an individual, at a particular a...
MYOCLONUS has been a subject of much thought, confusion and controversy in the past hundred years. R...
We describe three patients with Huntington's disease, from two families, in whom myoclonus was the p...
Myoclonus presents as a sudden brief jerk caused by involuntary muscle activity. An organisational f...
Clinical morphological and biochemical aspects of Familial Progressive Myoclonus Epilepsies are repo...
Myoclonus is a complex disorder of rapid repetitive muscle jerks that can occur in proximal or dista...
Myoclonus is defined as a brief and jerky shock-like involuntary movement caused by abrupt muscle co...
A clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy b
The term "myoclonus " sounds esoteric, yet it is part of our normal physiology, occurring ...
Background: Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characteri...
Physiological investigations continue to define the processes underlying different types of myoclonu...
This review examines some of the advances in understanding myoclonus over the last 25 years. The cla...
Few movement disorders seem to make a straightforward approach to diagnosis and treatment more diffi...
Genetically determined myoclonus disorders are a result of a large number of genes. They have wide c...
Myoclonus is a hyperkinetic movement disorder characterized by brief, involuntary muscular jerks. Re...
peer reviewedCan a gene defect be responsible for the occurrence in an individual, at a particular a...
MYOCLONUS has been a subject of much thought, confusion and controversy in the past hundred years. R...
We describe three patients with Huntington's disease, from two families, in whom myoclonus was the p...
Myoclonus presents as a sudden brief jerk caused by involuntary muscle activity. An organisational f...
Clinical morphological and biochemical aspects of Familial Progressive Myoclonus Epilepsies are repo...
Myoclonus is a complex disorder of rapid repetitive muscle jerks that can occur in proximal or dista...
Myoclonus is defined as a brief and jerky shock-like involuntary movement caused by abrupt muscle co...
A clinical, neurophysiological and genetic study of a familial form of myoclonic epilepsy b
The term "myoclonus " sounds esoteric, yet it is part of our normal physiology, occurring ...
Background: Autosomal dominant familial cortical myoclonic tremor and epilepsy (FCMTE) is characteri...
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