Počet záznamov: 1
myozitída s inklúznymi telieskami
SYS d018979 LBL 00000cx--j22000003--45-- 005 20240119200239.9 100 $a 19950524csloy0103----ba0 152 $b mesh 250 $a myozitída s inklúznymi telieskami $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 UR $x VE $x VI $8 slo 300 1-
$a 96 $8 eng 300 1-
$a Myositis (1968-1995) $8 eng 330 1-
$a Progressive myopathies characterized by the presence of inclusion bodies on muscle biopsy. Sporadic and hereditary forms have been described. The sporadic form is an acquired, adult-onset inflammatory vacuolar myopathy affecting proximal and distal muscles. Familial forms usually begin in childhood and lack inflammatory changes. Both forms feature intracytoplasmic and intranuclear inclusions in muscle tissue. (Adams et al., Principles of Neurology, 6th ed, pp1409-10) $8 eng 450 $a Inclusion Body Myositis $5 e $8 eng 450 $a Myopathy, Inclusion Body, Sporadic $5 e $8 eng 450 $a myopatia sporadická, s inklúznymi telieskami $5 e $8 slo 686 $a C05.651.594.600 686 $a C10.668.491.562.500 750 $a Myositis, Inclusion Body $8 eng 801 -0
$a US $b DNLM $c 19950524 801 -2
$a SK $b BA006 $c 20040622 820 $a do not coord with INCLUSION BODIES but coord with INCLUSION BODIES, VIRAL if relevant (IM or NIM) $8 eng 980 $x M
Počet záznamov: 1