Number of the records: 1  

epilepsia myoklonická juvenilná

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    $a epilepsia myoklonická juvenilná $x BL $x CF $x CI $x CL $x CN $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $2 slo
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    $w v $a Epilepsy, Myoclonic, Juvenile $2 eng
    450
      
    $w v $a Impulsive Petit Mal, Janz $2 eng
    450
      
    $w v $a Janz Syndrome $2 eng
    450
      
    $w v $a Juvenile Myoclonic Epilepsy $2 eng
    450
      
    $w v $a petit mal impulzívny, Janz $2 slo
    450
      
    $w v $a Janzov syndróm $2 slo
    450
      
    $w v $a epilepsia myoklonická adolescentná $2 slo
    450
      
    $w v $a petit mal impulzívny, epilepsia $2 slo
    450
      
    $w v $a JME (juvenilná myoklonická epilepsia) $2 slo
    450
      
    $w v $a Janzova juvenilná myoklonická epilepsia $2 slo
    450
      
    $w v $a petit mal impulzívny $2 slo
    665
      
    $a 2000 $2 eng
    665
      
    $a Epilepsies, Myoclonic (1977-1999) $2 eng
    665
      
    $a Epilepsy, Absence (1975-1999) $2 eng
    665
      
    $a Myoclonus (1975-1999) $2 eng
    680
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    $i A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323) $2 eng
    750
    -2
    $a Myoclonic Epilepsy, Juvenile $2 eng
    980
      
    $x M
Number of the records: 1  

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