Počet záznamov: 1
Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis
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$a eng $d eng 102 $a SK 200 1-
$a Aldosterone synthase deficiency type II: an unusual presentation of the first Greek case reported with confirmed genetic analysis $f Stayroula Papailiou ... [et al.] 320 $a Bibliogr. odkazy 320 $a Res. angl. 463 -1
$1 001 sllk_un_cat*0167330 $1 011 $a 1210-0668 $1 200 1 $a Endocrine regulations $v Vol. 54, no. 3 (2020), s. 227-229 $1 210 $a Bratislava $c Institute of Experimental Endocrinology $d 2020 $1 215 $a s. 157-229 606 1-
$3 sllk_un_auth*d019405 $a cytochróm P-450 CYP11B2 $x deficit $x genetika $x novorodenec $2 mesh 606 2-
$3 sllk_un_auth*d009154 $a mutácia $2 mesh 606 2-
$3 sllk_un_auth*d012816 $a príznaky a symptómy $2 mesh 606 2-
$3 sllk_un_auth*d003937 $a diagnostika diferenciálna $2 mesh 606 2-
$3 sllk_un_auth*d004358 $a farmakoterapia $2 mesh 606 2-
$3 sllk_un_auth*d007231 $a novorodenec $9 C $2 mesh 610 2-
$a deficiencia aldosterónsyntázy typ II 610 2-
$a mutácia génu CYP11B2 - variant c.554C>T (p.T185I) 610 2-
$a kazuistika 701 -1
$3 sllk_un_auth*0052258 $a Papailiou $b Stayroula $4 070 801 -0
$a SK $b BA006 $c 20200909 $g AACR2
Počet záznamov: 1