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Early myoclonic encephalopathy

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Review Articles from PubMed

Review articles summarize what is currently known about a disease. They discuss research previously published by others. The terms "Early myoclonic encephalopathy" returned 1 free, full-text review articles. First 1 results:
Early-onset epileptic encephalopathies: Ohtahara syndrome and early myoclonic encephalopathy.
Last Updated: Oct 09, 2012

Ohtahara syndrome and early myoclonic encephalopathy are the earliest presenting of the epileptic encephalopathies. They are typically distinguished from each other according to specific clinical and etiologic criteria. Nonetheless, considerable overlap exists between the two syndromes ...

Ohtahara syndrome: with special reference to its developmental aspects for differentiating from early myoclonic encephalopathy.
Last Updated: May 20, 2013

Ohtahara syndrome (OS) is well known as a peculiar early onset epileptic syndrome with serious prognosis. The outline of OS, mainly in relation to the evolution with age, and differentiation from related conditions, particularly early myoclonic encephalopathy (EME) were mentioned.

Are early myoclonic encephalopathy (EME) and the Ohtahara syndrome (EIEE) independent of each other?
Last Updated: Oct 26, 2015

Early myoclonic encephalopathy (EME) and the Ohtahara syndrome are currently listed as two separate syndromes in the classification of epilepsies. The most prominent differentiating points are the observations that patients with Ohtahara syndrome experience predominantly tonic seizures; ...

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Editorials from PubMed

Editorial articles describe the outcome of a single study. They are the published results of original research. The terms "Early myoclonic encephalopathy" returned 0 free, full-text editorial articles. First 0 results:
No publications were found for this category.
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Research Articles from PubMed

Research articles describe the outcome of a single study. They are the published results of original research. The terms "Early myoclonic encephalopathy" returned 10 free, full-text research articles. First few results:
Clinical features of early myoclonic encephalopathy caused by a CDKL5 mutation.
Last Updated: Jun 01, 2020

CDKL5 deficiency is caused by mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene and clinically manifests often in females as drug-resistant intractable epilepsy and severe psychomotor retardation.

Successful treatment of intractable life-threatening seizures with perampanel in the first case of early myoclonic encephalopathy with a novel de novo SCN1A mutation.
Last Updated: Mar 06, 2020

Early myoclonic encephalopathy (EME) is a form of developmental and epileptic encephalopathy with myoclonic seizures and a suppression burst on electroencephalogram, which occurs during the neonatal or early infantile period and is characterized by highly intractable seizures and ...

A case of early myoclonic encephalopathy with intractable seizures successfully treated with high-dose phenobarbital.
Last Updated: Jan 16, 2020

Early myoclonic encephalopathy (EME) is an epileptic syndrome that develops in neonates, commonly within 1 month of birth. The condition is characterized by irregular, partial, and asynchronous myoclonus. The seizures in EME are generally refractory to antiepileptic drugs and no ...

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10 Free Research Articles 31 Research Articles