Number of the records: 1  

glioblastóm

  1. SYSd005909
    LBL
      
    00000nz--a2200000o--4500
    005
      
    20250606213418.4
    008
      
    990101|||anznnbabn-----------|-a|a------
    040
      
    $b slo $a DNLM $d BA006
    065
      
    $a C04.557.465.625.600.380.080.335
    065
      
    $a C04.557.470.670.380.080.335
    065
      
    $a C04.557.580.625.600.380.080.335
    066
      
    $a 01 $c 03
    150
      
    $a glioblastóm $x BL $x BS $x CF $x CH $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 SC $x SU $x TH $x UL $x UR $x VE $x VI $2 slo
    450
      
    $w v $a Astrocytoma, Grade IV $2 eng
    450
      
    $w v $a Giant Cell Glioblastoma $2 eng
    450
      
    $w v $a Glioblastoma Multiforme $2 eng
    450
      
    $w v $a glioblastóm multiformný $2 slo
    450
      
    $w v $a glioblastoma multiforme $2 slo
    450
      
    $w v $a astrocytóm, IV. stupeň zrelosti $2 slo
    450
      
    $w v $a astrocytóm, IV. stupeň diferenciácie $2 slo
    450
      
    $w v $a glioblastóm obrovskobunkový $2 slo
    665
      
    $a 94; was GLIOBLASTOMA MULTIFORME 1963-93; GLIOBLASTOMA was see ASTROCYTOMA 1993 $2 eng
    680
    9-
    $i A malignant form of astrocytoma histologically characterized by pleomorphism of cells, nuclear atypia, microhemorrhage, and necrosis. They may arise in any region of the central nervous system, with a predilection for the cerebral hemispheres, basal ganglia, and commissural pathways. Clinical presentation most frequently occurs in the fifth or sixth decade of life with focal neurologic signs or seizures. $2 eng
    680
      
    $a coord IM with probably precoord CNS/neopl term + site (IM); for GLIOBLASTOMA WITH SARCOMATOUS COMPONENT see GLIOSARCOMA; for GLIOBLASTOMA, RETINAL see RETINOBLASTOMA $2 eng
    750
    -2
    $a Glioblastoma $2 eng
    980
      
    $x M
Number of the records: 1  

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