Number of the records: 1  

Charcotova-Marieho-Toothova choroba

  1. SYSd002607
    LBL
      
    00000cx--j2200000---45--
    005
      
    20240119201446.0
    100
      
    $a 19991108asloy0103----ba0
    152
      
    $b mesh
    250
      
    $a Charcotova-Marieho-Toothova choroba $x BL $x CF $x CI $x CL $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(1966) $8 eng
    330
    1-
    $a A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343) $8 eng
    450
      
    $a Atrophy, Muscular, Peroneal $5 e $8 eng
    450
      
    $a HMSN Type I $5 e $8 eng
    450
      
    $a HMSN Type II $5 e $8 eng
    450
      
    $a Hereditary Motor and Sensory-Neuropathy Type II $5 e $8 eng
    450
      
    $a Hereditary Motor, and Sensory Neuropathy Type I $5 e $8 eng
    450
      
    $a Muscular Atrophy, Peroneal $5 e $8 eng
    450
      
    $a Peroneal Muscular Atrophy $5 e $8 eng
    450
      
    $a Roussy-Levy Syndrome $5 e $8 eng
    450
      
    $a Charcotova-Marieho choroba $5 e $8 slo
    450
      
    $a atrofia svalová peroneálna $5 e $8 slo
    450
      
    $a atrofia muskulárna peroneálna $5 e $8 slo
    450
      
    $a neuropatia hereditárna motoricko-senzitívna $5 e $8 slo
    450
      
    $a neuropatia dedičná motorická a senzorická, typ I $5 e $8 slo
    450
      
    $a neuropatia dedičná motorická a senzorická, typ II $5 e $8 slo
    450
      
    $a HMSN, typ I $5 e $8 slo
    450
      
    $a HMSN, typ II $5 e $8 slo
    450
      
    $a dystrofia svalová peroneálna $5 e $8 slo
    450
      
    $a dystrofia muskulárna peroneálna $5 e $8 slo
    450
      
    $a Roussyho-Lévyho syndróm $5 e $8 slo
    450
      
    $a CMT choroba $5 e $8 slo
    550
      
    $3 sllk_un_auth*d018993 $Y Myelin P0 Protein $5 F $a proteín myelínový P0
    550
      
    $3 sllk_un_auth*d018993 $Y Myelin P0 Protein $5 B $a proteín myelínový P0
    550
      
    $3 sllk_un_auth*d051767 $Y Early Growth Response Protein 2 $5 B $a proteín Egr-2
    686
      
    $a C10.500.300.200
    686
      
    $a C10.574.500.495.200
    686
      
    $a C10.668.829.800.300.200
    686
      
    $a C16.131.666.300.200
    686
      
    $a C16.320.400.375.200
    750
      
    $a Charcot-Marie-Tooth Disease $8 eng
    801
    -0
    $a US $b DNLM $c 19991108
    801
    -2
    $a SK $b BA006 $c 20011024
    801
    -2
    $a SK $b BA006 $c 20100422
    801
    -2
    $a SK $b BA006 $c 20150813
    980
      
    $x M
Number of the records: 1  

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