Number of the records: 1
myozitída s inklúznymi telieskami
SYS d018979 LBL 00000cz--a2200000o--4500 005 20250606214351.0 008 950524|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C05.651.594.600 065 $a C10.668.491.562.500 066 $a 01 $c 03 150 $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 $2 slo 450 $w v $a Inclusion Body Myositis $2 eng 450 $w v $a Myopathy, Inclusion Body, Sporadic $2 eng 450 $w v $a myopatia sporadická, s inklúznymi telieskami $2 slo 665 $a 96 $2 eng 665 $a Myositis (1968-1995) $2 eng 680 9-
$i 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) $2 eng 680 $a do not coord with INCLUSION BODIES but coord with INCLUSION BODIES, VIRAL if relevant (IM or NIM) $2 eng 750 -2
$a Myositis, Inclusion Body $2 eng 980 $x M
Number of the records: 1