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Gerstmannova-Sträusslerova-Scheinkerova choroba
SYS d016098 LBL 00000cx--j22000003--45-- 005 20240119200126.5 100 $a 19920606csloy0103----ba0 152 $b mesh 250 $a Gerstmannova-Sträusslerova-Scheinkerova choroba $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 2000(1991); use SLOW VIRUS DISEASES 1988-1990; GERSTMANN-STRAUSSLER-SCHEINKER DISEASE was GERSTMANN-STRAUSSLER-SCHEINDER DISEASE see GERSTMANN-STRAUSSLER SYNDROME 1991 $8 eng 300 1-
$a Slow Virus Diseases (1988-1990) $8 eng 330 1-
$a An autosomal dominant familial prion disease with a wide spectrum of clinical presentations including ATAXIA, spastic paraparesis, extrapyramidal signs, and DEMENTIA. Clinical onset is in the third to sixth decade of life and the mean duration of illness prior to death is five years. Several kindreds with variable clinical and pathologic features have been described. Pathologic features include cerebral prion protein amyloidosis, and spongiform or neurofibrillary degeneration. (From Brain Pathol 1998 Jul;8(3):499-513; Brain Pathol 1995 Jan;5(1):61-75) $8 eng 450 $a Gerstmann-Straussler Syndrome $5 e $8 eng 450 $a encefalopatia cerebelárna spongiformná chronická $5 e $8 slo 450 $a Gerstmannov-Sträusslerov syndróm $5 e $8 slo 686 $a C01.207.800.350 686 $a C10.228.228.800.350 686 $a C10.574.500.425 686 $a C10.574.843.400 686 $a C16.320.400.350 750 $a Gerstmann-Straussler-Scheinker Disease $8 eng 801 -0
$a US $b DNLM $c 19920606 801 -2
$a SK $b BA006 $c 20050610 820 $a a prion dis: do not confuse with GERSTMANN SYNDROME, a type of agnosia $8 eng 980 $x M
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