Number of the records: 1
epilepsia rolandická
SYS d019305 LBL 00000cx--j2200000---45-- 005 20240119200248.3 100 $a 19960613asloy0103----ba0 152 $b mesh 250 $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 $8 slo 300 1-
$a 1997 $8 eng 300 1-
$a Epilepsy, Partial (1986-1996) $8 eng 330 1-
$a 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) $8 eng 450 $a Benign Childhood Epilepsy With Centro-Temporal Spikes $5 e $8 eng 450 $a Benign Epilepsy With Centrotemporal Spikes $5 e $8 eng 450 $a Benign Rolandic Epilepsy of Childhood $5 e $8 eng 450 $a Epilepsy, Centrotemporal $5 e $8 eng 450 $a Rolands Epilepsy $5 e $8 eng 450 $a Sylvian Epilepsy $5 e $8 eng 450 $a epilepsia s rolandickými hrotmi $5 e $8 slo 450 $a epilepsia centrotemporálna $5 e $8 slo 450 $a epilepsia benígna detská, s centrotemporálnymi hrotmi $5 e $8 slo 450 $a epilepsia benígna detská, s rolandickými hrotmi $5 e $8 slo 450 $a epilepsia benígna rolandická detská $5 e $8 slo 450 $a Sylviova epilepsia $5 e $8 slo 686 $a C10.228.140.490.360.280 686 $a C10.228.140.490.493.250 750 $a Epilepsy, Rolandic $8 eng 801 -0
$a US $b DNLM $c 19960613 801 -2
$a SK $b BA006 $c 20010523 801 -2
$a SK $b BA006 $c 20101220 980 $x M
Number of the records: 1