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Essential palatal myoclonus with spontaneous resolution: a rare case report. [PDF]
Ann Med Surg (Lond)Lamichhane P +4 more
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Case Report: Creutzfeldt-Jakob disease and diagnosis challenges: case report and evidence synthesis. [PDF]
F1000ResFailoc Rojas VE +5 more
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Defining the Rhythm: Developing a New Method to Describe Tremor and Myoclonus. [PDF]
Mov DisordLatorre A +6 more
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Lance-Adams Syndrome: An Updated Review of a Rare Post-Hypoxic Complication. [PDF]
Tremor Other Hyperkinet Mov (N Y)Malakooti M +10 more
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Neurodevelopmental Disorder and Cortical Myoclonus in ZMYM2 Deficiency. [PDF]
Mov DisordPollini L +6 more
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Current Treatment Options in Neurology, 2005
Myoclonus is defined as sudden, brief, shock-like involuntary movements affecting one or more muscles. The term encompasses a wide range of different physiologic and pathologic processes. When evaluating a patient with myoclonus, the first step is to identify the underlying etiology.
Melissa J, Nirenberg, Steven J, Frucht
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Myoclonus is defined as sudden, brief, shock-like involuntary movements affecting one or more muscles. The term encompasses a wide range of different physiologic and pathologic processes. When evaluating a patient with myoclonus, the first step is to identify the underlying etiology.
Melissa J, Nirenberg, Steven J, Frucht
openaire +2 more sources
Current Opinion in Neurology, 1995
Genetic studies have suggested homogeneity between the Baltic-type and Mediterranean-type progressive myoclonic epilepsy. Magnetoencephalography was applied to elucidate the mechanism underlying the giant evoked responses in cortical reflex myoclonus. A new concept of negative myoclonus mediated by cortical reflex mechanism was proposed.
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Genetic studies have suggested homogeneity between the Baltic-type and Mediterranean-type progressive myoclonic epilepsy. Magnetoencephalography was applied to elucidate the mechanism underlying the giant evoked responses in cortical reflex myoclonus. A new concept of negative myoclonus mediated by cortical reflex mechanism was proposed.
openaire +2 more sources
Myoclonus-Dystonia/Essential Myoclonus☆
2010Myoclonus-dystonia (M-D, formerly known as ‘Hereditary essential myoclonus’) is a rare movement disorder characterized by myoclonic jerks and dystonic movements or postures. M-D has an autosomal dominant inheritance with reduced penetrance because of maternal imprinting and is caused by mutations in the ϵ-sarcoglycan gene (SGCE) on chromosome 7q21.
Peall, K. J. +2 more
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Current Treatment Options in Neurology, 2000
The diagnosis and treatment of myoclonus pose a particular challenge to the neurologist. Few well-controlled double-blind studies of antimyoclonic agents have been performed, and clinical rating of the effectiveness of treatment has been primarily descriptive. As a result, therapy is often empiric. This article reviews the author's approach to treating
openaire +2 more sources
The diagnosis and treatment of myoclonus pose a particular challenge to the neurologist. Few well-controlled double-blind studies of antimyoclonic agents have been performed, and clinical rating of the effectiveness of treatment has been primarily descriptive. As a result, therapy is often empiric. This article reviews the author's approach to treating
openaire +2 more sources