Number of the records: 1  

degenerácie spinocerebelárne

  1. SYSd013132
    LBL
      
    00000cz--a2200000o--4500
    005
      
    20250606214722.4
    008
      
    920331|||anznnbabn-----------|-a|a------
    040
      
    $b slo $a DNLM $d BA006
    065
      
    $a C10.228.140.252.700
    065
      
    $a C10.228.854.787
    065
      
    $a C10.574.500.825
    065
      
    $a C16.320.400.780
    066
      
    $a 01 $c 03
    150
      
    $a degenerácie spinocerebelárne $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 Ataxias, Hereditary $2 eng
    450
      
    $w v $a Cerebellar Ataxia, Early Onset $2 eng
    450
      
    $w v $a Cerebellar Ataxia, Late Onset $2 eng
    450
      
    $w v $a Cerebellar Degenerations, Primary $2 eng
    450
      
    $w v $a Corticostriatal-Spinal Degeneration $2 eng
    450
      
    $w v $a Marie Cerebellar Ataxia $2 eng
    450
      
    $w v $a Marinesco-Sjogren Syndrome $2 eng
    450
      
    $w v $a Spinocerebellar Degeneration $2 eng
    450
      
    $w v $a Marinescov-Sjögrenov syndróm $2 slo
    450
      
    $w v $a ataxie dedičné $2 slo
    450
      
    $w v $a degenerácia spinocerebelárna $2 slo
    450
      
    $w v $a ataxia cerebelárna, skorý nástup $2 slo
    450
      
    $w v $a ataxia cerebelárna, neskorý nástup $2 slo
    450
      
    $w v $a degenerácie cerebelárne primárne $2 slo
    450
      
    $w v $a degenerácia kortikostriatálno-spinálna $2 slo
    450
      
    $w v $a Marieho cerebelárna ataxia $2 slo
    450
      
    $w v $a syndroma Marie $2 slo
    665
      
    $a 2000(1987) $2 eng
    665
      
    $a Cerebellar Ataxia (1968-1986) $2 eng
    665
      
    $a Cerebellar Diseases (1966-1986) $2 eng
    665
      
    $a Spinal Cord Diseases (1966-1986) $2 eng
    680
    9-
    $i A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked. $2 eng
    750
    -2
    $a Spinocerebellar Degenerations $2 eng
    980
      
    $x M
Number of the records: 1  

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