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gangliozidózy
SYS d005733 LBL 00000nx--j22000003--45-- 005 20240119201100.7 100 $a 19920723csloy0103----ba0 152 $b mesh 250 $a gangliozidózy $x BL $x CF $x CI $x CL $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 1992(1976) $8 eng 300 1-
$a Gangliosides (1966-1975) $8 eng 300 1-
$a Lipoidosis (1966-1975) $8 eng 330 1-
$a A group of autosomal recessive lysosomal storage disorders marked by the accumulation of GANGLIOSIDES. They are caused by impaired enzymes or defective cofactors required for normal ganglioside degradation in the LYSOSOMES. Gangliosidoses are classified by the specific ganglioside accumulated in the defective degradation pathway. $8 eng 550 $3 sllk_un_auth*d005696 $Y Galactosidases $5 B $a galaktozidázy 550 $3 sllk_un_auth*d009081 $Y Mucolipidoses $5 F $a mukolipidózy 550 $3 sllk_un_auth*d006596 $Y Hexosaminidases $5 B $a hexozaminidázy 550 $3 sllk_un_auth*d009081 $Y Mucolipidoses $5 B $a mukolipidózy 686 $a C10.228.140.163.100.435.825.300 686 $a C16.320.565.189.435.825.300 686 $a C16.320.565.398.641.803.350 686 $a C16.320.565.595.554.825.300 686 $a C18.452.132.100.435.825.300 686 $a C18.452.584.563.641.803.350 686 $a C18.452.648.189.435.825.300 686 $a C18.452.648.398.641.803.350 686 $a C18.452.648.595.554.825.300 750 $a Gangliosidoses $8 eng 801 -0
$a US $b DNLM $c 19920723 801 -2
$a SK $b BA006 $c 20070706 820 $a coordinate IM with specific ganglioside (IM) but GANGLIOSIDOSIS, GM1 and GANGLIOSIDOSES, GM2 are available $8 eng 980 $x M
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