Skip to search formSkip to main contentSkip to account menu
You are currently offline. Some features of the site may not work correctly.

Myoclonic Epilepsy, Juvenile

Known as: Myoclonic Epilepsy, Juvenile, 1, Impulsive Petit Mal, Janz, Myoclonic Epilepsies, Adolescent 
A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE… 
National Institutes of Health

Related topics

Related topics

14 relations
Absence EpilepsyAutosomal dominant inheritanceBrainCentral Nervous System
Expand

Narrower (1)

Epilepsies, Myoclonic

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Literature Review
  • J. Gagné
  • Journal of ultrasound in medicine : official…
  • 2018
  • Corpus ID: 1534407
Microemulsions are clear, stable, isotropic mixtures of oil, water and surfactant, frequently in combination with a cosurfactant… 
Highly Cited
2017
Highly Cited
2017
Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology
The International League Against Epilepsy (ILAE) presents a revised operational classification of seizure types. The purpose of… 
Highly Cited
2005
Highly Cited
2005
Counting the dead and what they died from: an assessment of the global status of cause of death data.
OBJECTIVE We sought to assess the current status of global data on death registration and to examine several indicators of data… 
  • table 1
  • table 3
  • table 4
  • table 2
Highly Cited
2002
Highly Cited
2002
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy
Although many genes that predispose for epilepsy in humans have been determined, those that underlie the classical syndromes of… 
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Review
2000
Review
2000
Dysfunction in the neural circuitry of emotion regulation--a possible prelude to violence.
Emotion is normally regulated in the human brain by a complex circuit consisting of the orbital frontal cortex, amygdala… 
Review
1999
Review
1999
Varieties of impulsivity
  • J. Evenden
  • Psychopharmacology
  • 1999
  • Corpus ID: 5972342
Abstract The concept of impulsivity covers a wide range of ”actions that are poorly conceived, prematurely expressed, unduly… 
  • table 1
  • table 3
  • table 5
  • table 6
Highly Cited
1998
Highly Cited
1998
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
Parkinson's disease is a common neurodegenerative disease with complex clinical features. Autosomal recessive juvenile… 
Highly Cited
1997
Highly Cited
1997
Dentate Granule Cell Neurogenesis Is Increased by Seizures and Contributes to Aberrant Network Reorganization in the Adult Rat Hippocampus
The dentate granule cell layer of the rodent hippocampal formation has the distinctive property of ongoing neurogenesis that… 
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Highly Cited
1993
Highly Cited
1993
Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A.
Genetic and metabolic studies have been done on a large kindred in which several males are affected by a syndrome of borderline… 
Review
1985
Review
1985
Epilepsy with impulsive petit mal (Juvenile Myoclonic Epilepsy)
  • D. Janz
  • Acta neurologica Scandinavica
  • 1985
  • Corpus ID: 29713546
ABSTRACT – Juvenile myoclonic epilepsy (JME) is a special syndrome within the primary generalized epilepsies which is… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy, Terms of Service, and Dataset License
ACCEPT & CONTINUE