Počet záznamov: 1  

Duchenneova svalová dystrofia

  1. SYSd020388
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    20250606214044.7
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    991108|||anznnbabn-----------|-a|a------
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    $b slo $a DNLM $d BA006 $a BA006 $d BA006
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    $a C05.651.534.500.300
    065
      
    $a C10.668.491.175.500.300
    065
      
    $a C16.320.322.562
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    $a C16.320.577.300
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    $a 01 $c 03
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    $a 616.74-056.7
    089
      
    $a 616.8-009.5
    150
      
    $a Duchenneova svalová dystrofia $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 VI $2 slo
    450
      
    $w v $a Becker Muscular Dystrophy $2 eng
    450
      
    $w v $a Duchenne Muscular Dystrophy $2 eng
    450
      
    $w v $a Muscular Dystrophy, Becker $2 eng
    450
      
    $w v $a Muscular Dystrophy, Pseudohypertrophic $2 eng
    450
      
    $w v $a Beckerova svalová dystrofia $2 slo
    450
      
    $w v $a dystrofia svalová pseudohypertrofická $2 slo
    450
      
    $w v $a Duchenneova pseudohypertrofická svalová dystrofia $2 slo
    450
      
    $w v $a Duchennova svalová dystrofia $2 slo
    550
      
    $7 sllk_us_auth*d016189 $Y Dystrophin $w b $a dystrofín
    550
      
    $7 sllk_us_auth*d016189 $Y Dystrophin $w p $a dystrofín
    665
      
    $a 2000; use MUSCULAR DYSTROPHIES 1980-1999; for MUSCULAR DYSTROPHY, BECKER & BECKER MUSCULAR DYSTROPHY use MUSCULAR DYSTROPHIES 1991-1999 $2 eng
    665
      
    $a Muscular Dystrophies (1966-1999) $2 eng
    680
    9-
    $i An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415) $2 eng
    750
    -2
    $a Muscular Dystrophy, Duchenne $2 eng
    980
      
    $x M
Počet záznamov: 1  

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