Number of the records: 1
prionózy
SYS d017096 LBL 00000cz--a2200000o--4500 005 20250606213534.3 008 920522|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C01.207.800 065 $a C10.228.228.800 065 $a C10.574.843 066 $a 01 $c 03 150 $a prionózy $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 $2 slo 450 $w v $a Dementias, Transmissible $2 eng 450 $w v $a Spongiform Encephalopathies, Transmissible $2 eng 450 $w v $a Transmissible Dementias $2 eng 450 $w v $a choroby priónové $2 slo 450 $w v $a encefalopatie spongiformné prenosné $2 slo 450 $w v $a encefalopatie spongioformné prenosné $2 slo 450 $w v $a encefalopatie špongioformné prenosné $2 slo 450 $w v $a demencie prenosné $2 slo 550 $7 sllk_us_auth*d012608 $Y Scrapie $w b $a scrapie 550 $7 sllk_us_auth*d012897 $Y Slow Virus Diseases $w b $a infekcie pomalé vírusové 665 $a 1993 $2 eng 665 $a Slow Virus Diseases (1966-1992) $2 eng 680 9-
$i A group of genetic, infectious, or sporadic degenerative human and animal nervous system disorders associated with abnormal PRIONS. These diseases are characterized by conversion of the normal prion protein to an abnormal configuration via a post-translational process. In humans, these conditions generally feature DEMENTIA; ATAXIA; and a fatal outcome. Pathologic features include a spongiform encephalopathy without evidence of inflammation. The older literature occasionally refers to these as unconventional SLOW VIRUS DISEASES. (From Proc Natl Acad Sci USA 1998 Nov 10;95(23):13363-83) $2 eng 680 $a general or unspecified; prefer specifics $2 eng 750 -2
$a Prion Diseases $2 eng 980 $x M
Number of the records: 1