Number of the records: 1  

neurofibromatózy

  1. SYSd017253
    LBL
      
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    20240119200155.1
    100
      
    $a 19920522asloy0103----ba0
    152
      
    $b mesh
    250
      
    $a neurofibromatózy $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 2000(1993) $8 eng
    330
    1-
    $a A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72) $8 eng
    450
      
    $a Neurofibromatosis $5 e $8 eng
    450
      
    $a Neurofibromatosis Type 3 $5 e $8 eng
    450
      
    $a neurofibromatóza $5 e $8 slo
    450
      
    $a neurofibromatóza, typ 3 $5 e $8 slo
    450
      
    $a neurofibromatóza typu 3 $5 e $8 slo
    686
      
    $a C04.557.580.600.580.590
    686
      
    $a C04.700.631
    686
      
    $a C10.562.600
    686
      
    $a C10.574.500.549
    686
      
    $a C16.320.400.560
    686
      
    $a C16.320.700.633
    750
      
    $a Neurofibromatoses $8 eng
    801
    -0
    $a US $b DNLM $c 19920522
    801
    -2
    $a SK $b BA006 $c 20001114
    801
    -2
    $a SK $b BA006 $c 20101222
    820
      
    $a multiple neurofibromas; specifics are available $8 eng
    980
      
    $x M
Number of the records: 1  

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