Počet záznamov: 1  

skleróza tuberózna

  1. SYSd014402
    LBL
      
    00000cz--a2200000n--4500
    005
      
    20250606213819.8
    008
      
    990101|||anznnbabn-----------|-a|a------
    040
      
    $b slo $a DNLM $d BA006 $d BA006 $d BA006
    065
      
    $a C04.445.810
    065
      
    $a C04.651.800
    065
      
    $a C04.700.700
    065
      
    $a C10.500.507.400.750
    065
      
    $a C10.562.850
    065
      
    $a C10.574.500.865
    065
      
    $a C16.131.666.507.400.750
    065
      
    $a C16.320.400.880
    065
      
    $a C16.320.700.700
    066
      
    $a 01 $c 03
    089
      
    $a 616.831-004 $v UDC-MRF-SK3 $z slo
    150
      
    $a skleróza tuberózna $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 Bourneville Disease $2 eng
    450
      
    $w v $a Epiloia $2 eng
    450
      
    $w v $a Phakomatosis, Bourneville $2 eng
    450
      
    $w v $a Bournevilleov syndróm $2 slo
    450
      
    $w v $a Bournevillov syndróm $2 slo
    450
      
    $w v $a Bournevilleov-Pringleov syndróm $2 slo
    450
      
    $w v $a Bournevillov-Pringleov syndróm $2 slo
    450
      
    $w v $a Bournevilleova-Pringleova choroba $2 slo
    450
      
    $w v $a Bournevillova-Pringleova choroba $2 slo
    450
      
    $w v $a Bournevilleova choroba $2 slo
    450
      
    $w v $a Bournevillova choroba $2 slo
    450
      
    $w v $a epiloia $2 slo
    450
      
    $w v $a Bournevilleova fakomatóza $2 slo
    450
      
    $w v $a skleróza mozgová $2 slo
    450
      
    $w v $a sclerosis tuberosa $2 slo
    450
      
    $w v $a komplex tuberóznej sklerózy $2 slo
    450
      
    $w v $a adenoma sebaceum $2 slo
    450
      
    $w v $a skleróza cerebrálna $2 slo
    550
      
    $7 sllk_us_auth*d005350 $Y Fibroma $w b $a fibróm
    680
    9-
    $i Autosomal dominant neurocutaneous syndrome classically characterized by MENTAL RETARDATION; EPILEPSY; and skin lesions (e.g., adenoma sebaceum and hypomelanotic macules). There is, however, considerable heterogeneity in the neurologic manifestations. It is also associated with cortical tuber and HAMARTOMAS formation throughout the body, especially the heart, kidneys, and eyes. Mutations in two loci TSC1 and TSC2 that encode hamartin and tuberin, respectively, are associated with the disease. $2 eng
    750
    -2
    $a Tuberous Sclerosis $2 eng
    980
      
    $x M
Počet záznamov: 1  

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