Number of the records: 1
Creutzfeldtov-Jakobov syndróm
SYS d007562 LBL 00000cx--j2200000---45-- 005 20240119195742.1 100 $a 19990101asloy0103----ba0 152 $b mesh 250 $a Creutzfeldtov-Jakobov syndróm $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 TM $x UR $x VE $x VI $8 slo 300 1-
$a 1991; use JAKOB-CREUTZFELDT SYNDROME 1981-1990, use CREUTZFELDT-JAKOB DISEASE 1969-1980 $8 eng 300 1-
$a Central Nervous System Diseases (1966-1968) $8 eng 330 1-
$a A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27)) $8 eng 450 $a New Variant Creutzfeldt-Jakob Disease $5 e $8 eng 450 $a Spongiform Encephalopathy, Subacute $5 e $8 eng 450 $a Jakobov-Creutzfeldtov syndróm $5 e $8 slo 450 $a vCJD $5 e $8 slo 450 $a CJD variantná $5 e $8 slo 450 $a Creutzfeldt-Jakobova choroba, nový variant $5 e $8 slo 450 $a encefalopatia spongiformná subakútna $5 e $8 slo 450 $a encefalopatia spongioformná subakútna $5 e $8 slo 450 $a encefalopatia špongiformná subakútna $5 e $8 slo 686 $a C01.207.800.230 686 $a C10.228.140.380.165 686 $a C10.228.228.800.230 686 $a F03.615.400.300 750 $a Creutzfeldt-Jakob Syndrome $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20060727 801 -2
$a SK $b BA006 $c 20101220 980 $x M
Number of the records: 1