Number of the records: 1  

epilepsia rolandická

  1. SYSd019305
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    20250606213730.0
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    $b slo $a DNLM $d BA006 $d BA006
    065
      
    $a C10.228.140.490.360.280
    065
      
    $a C10.228.140.490.493.250
    066
      
    $a 01 $c 03
    150
      
    $a epilepsia rolandická $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
    450
      
    $w v $a Benign Childhood Epilepsy With Centro-Temporal Spikes $2 eng
    450
      
    $w v $a Benign Epilepsy With Centrotemporal Spikes $2 eng
    450
      
    $w v $a Benign Rolandic Epilepsy of Childhood $2 eng
    450
      
    $w v $a Epilepsy, Centrotemporal $2 eng
    450
      
    $w v $a Rolands Epilepsy $2 eng
    450
      
    $w v $a Sylvian Epilepsy $2 eng
    450
      
    $w v $a epilepsia s rolandickými hrotmi $2 slo
    450
      
    $w v $a epilepsia centrotemporálna $2 slo
    450
      
    $w v $a epilepsia benígna detská, s centrotemporálnymi hrotmi $2 slo
    450
      
    $w v $a epilepsia benígna detská, s rolandickými hrotmi $2 slo
    450
      
    $w v $a epilepsia benígna rolandická detská $2 slo
    450
      
    $w v $a Sylviova epilepsia $2 slo
    665
      
    $a 1997 $2 eng
    665
      
    $a Epilepsy, Partial (1986-1996) $2 eng
    680
    9-
    $i An autosomal dominant inherited partial epilepsy syndrome with onset between age 3 and 13 years. Seizures are characterized by PARESTHESIA and tonic or clonic activity of the lower face associated with drooling and DYSARTHRIA. In most cases, affected children are neurologically and developmentally normal. (From Epilepsia 1998 39;Suppl 4:S32-S41) $2 eng
    750
    -2
    $a Epilepsy, Rolandic $2 eng
    980
      
    $x M
Number of the records: 1  

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