Počet záznamov: 1
epidermolysis bullosa dystrophica
SYS d016108 LBL 00000nx--j22000003--45-- 005 20240119200126.7 100 $a 19920212csloy0103----ba0 152 $b mesh 250 $a epidermolysis bullosa dystrophica $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 1991 $8 eng 300 1-
$a Epidermolysis Bullosa (1966-1990) $8 eng 330 1-
$a Form of epidermolysis bullosa characterized by atrophy of blistered areas, severe scarring, and nail changes. It is most often present at birth or in early infancy and occurs in both autosomal dominant and recessive forms. All forms of dystrophic epidermolysis bullosa result from mutations in COLLAGEN TYPE VII, a major component fibrils of BASEMENT MEMBRANE and EPIDERMIS. $8 eng 450 $a Cockayne-Touraine Disease $5 e $8 eng 450 $a Epidermolysis Bullosa, Dystrophic $5 e $8 eng 450 $a Hallopeau-Siemens Disease $5 e $8 eng 686 $a C16.131.831.493.160 686 $a C16.320.850.275.160 686 $a C17.300.200.367 686 $a C17.800.804.493.160 686 $a C17.800.827.275.160 686 $a C17.800.865.410.160 750 $a Epidermolysis Bullosa Dystrophica $8 eng 801 -0
$a US $b DNLM $c 19920212 801 -2
$a SK $b BA006 $c 20070706 980 $x M
Počet záznamov: 1