Počet záznamov: 1
angioedémy dedičné, typ I a II
SYS d056829 LBL 00000nx--j2200000---45-- 005 20240119201506.2 100 $a 20100101asloy0103----ba0 152 $b mesh 250 $a angioedémy dedičné, typ I a II $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 2010 $8 eng 300 1-
$a Angioedema (1964-2007) $8 eng 300 1-
$a Angioedemas, Hereditary (2007-2009) $8 eng 330 1-
$a Forms of hereditary angioedema that occur due to mutations in the gene for COMPLEMENT C1 INHIBITOR PROTEIN. Type I hereditary angioedema is associated with reduced serum levels of complement C1 inhibitor protein. Type II hereditary angioedema is associated with the production of a non-functional complement C1 inhibitor protein. $8 eng 450 $a angioedémy hereditárne typu I a II $5 e $8 slo 550 $3 sllk_un_auth*d050718 $Y Complement C1 Inhibitor Protein $5 F $a proteín inhibujúci komplement C1 686 $a C14.907.079.500.750 686 $a C17.800.862.945.066.500.750 686 $a C20.543.480.904.066.500.750 750 $a Hereditary Angioedema Types I and II $8 eng 801 -0
$a SK $b BA006 $c 20100316 801 -2
$a SK $b BA006 $c 20100706 980 $x M
Počet záznamov: 1