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paralýzy familiárne periodické
SYS d010245 LBL 00000cx--j22000003--45-- 005 20240119195852.8 100 $a 19990101csloy0103----ba0 152 $b mesh 250 $a paralýzy familiárne periodické $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(1966) $8 eng 330 1-
$a A heterogenous group of inherited disorders characterized by recurring attacks of rapidly progressive flaccid paralysis or myotonia. These conditions have in common a mutation of the gene encoding the alpha subunit of the sodium channel in skeletal muscle. They are frequently associated with fluctuations in serum potassium levels. Periodic paralysis may also occur as a non-familial process secondary to THYROTOXICOSIS and other conditions. (From Adams et al., Principles of Neurology, 6th ed, p1481) $8 eng 450 $a Normokalemic Periodic Paralysis $5 e $8 eng 450 $a Periodic Paralysis, Familial $5 e $8 eng 450 $a paralýza periodická normokaliemická $5 e $8 slo 450 $a paralýza familiárna periodická $5 e $8 slo 686 $a C05.651.701 686 $a C10.668.491.650 686 $a C16.320.565.618.711 686 $a C18.452.648.618.711 750 $a Paralyses, Familial Periodic $8 eng 801 -0
$a US $b DNLM $c 19990101 801 -2
$a SK $b BA006 $c 20020711 820 $a a specific disease entity: see MeSH definition $8 eng 980 $x M
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