Results 61 to 70 of about 6,575 (206)

Teaching NeuroImages: Leukodystrophy and progressive myoclonic epilepsy disclosing DRPLA [PDF]

open access: yes, 2016
A 25-year-old Brazilian man presented with an 8-year history of progressive myoclonic epilepsy. Familial history disclosed a Japanese paternal grandmother with late-onset parkinsonism-dementia and a paternal uncle with atypical parkinsonism.
Vieira de Rezende Pinto, Wladimir Bocca [UNIFESP]   +3 more
core   +1 more source

Timing is everything: The effect of early‐life seizures on developing neuronal circuits subserving spatial memory

open access: yesEpilepsia Open, EarlyView.
Abstract Spatial memory, the aspect of memory involving encoding and retrieval of information regarding one's environment and spatial orientation, is a complex biological function incorporating multiple neuronal networks. Hippocampus‐dependent spatial memory is not innate and emerges during development in both humans and rodents.
Gregory L. Holmes
wiley   +1 more source

Epilepsy syndromes classification

open access: yesEpilepsia Open, EarlyView.
Abstract Epilepsy syndromes are distinct electroclinical entities which have been recently defined by the International League Against Epilepsy Nosology and Definitions Task Force. Each syndrome is associated with “a characteristic cluster of clinical and EEG features, often supported by specific etiologic findings”.
Elaine C. Wirrell   +4 more
wiley   +1 more source

Motor responses to afferent stimulation in juvenile myoclonic epilepsy. [PDF]

open access: yes, 2004
PURPOSE: To document whether the mechanisms responsible for myoclonic jerks in juvenile myoclonic epilepsy (JME) are similar to those causing other forms of myoclonus.
Bongiovanni L. G.   +7 more
core   +1 more source

Prevention of etomidate-related myoclonus in anesthetic induction by pretreatment with magnesium

open access: yesJournal of Research in Medical Sciences, 2011
Background: Etomidate frequently leads to myoclonic jerks during anesthetic induction. This study aimed to detect if pretreatment with magnesium decreases myoclonus incidence.
Bulent Un, Dilek Ceyhan, Birgul Yelken
doaj  

Unique EEG signature of atypical absence seizures in SYNGAP1‐related developmental and epileptic encephalopathy

open access: yes
Epileptic Disorders, EarlyView.
Rainier Mark Loidor L. Rapal   +2 more
wiley   +1 more source

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

open access: yesEpilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola   +3 more
wiley   +1 more source

Juvenile myoclonic epilepsy of Janz: clinical observations in 60 patients [PDF]

open access: yes, 1992
We studied 60 patients with juvenile myoclonic epilepsy (JME). There was a high positive family history for epilepsy (33.3%). Age at onset of epilepsy ranged from 4 to 18 years with an average of 13.9 years. 88.3% of patients were seizure-free.
L. Minotti   +7 more
core   +1 more source

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