about
Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus-benefit of genetic testing.Diseases caused by defects of energy level and loss of coherence in living cells.High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.Post-natal growth of 157 children born as extremely premature neonates.Five-year survival without major disability of extremely preterm infants born at 22-27 weeks' gestation admitted to a NICU.Isoelectric Focusing of Serum Apolipoprotein C-III as a Sensitive Screening Method for the Detection of O-glycosylation Disturbances
P50
description
pediatrička, endokrinoložka
@cs
researcher ORCID ID = 0000-0003-1144-3440
@en
wetenschapper
@nl
name
Jitka Kytnarová
@ast
Jitka Kytnarová
@cs
Jitka Kytnarová
@en
Jitka Kytnarová
@es
Jitka Kytnarová
@nl
type
label
Jitka Kytnarová
@ast
Jitka Kytnarová
@cs
Jitka Kytnarová
@en
Jitka Kytnarová
@es
Jitka Kytnarová
@nl
altLabel
Kytnarova J
@en
Kytnarová J
@en
prefLabel
Jitka Kytnarová
@ast
Jitka Kytnarová
@cs
Jitka Kytnarová
@en
Jitka Kytnarová
@es
Jitka Kytnarová
@nl
P106
P214
P1053
K-2879-2017
P1153
6602614403
P19
P21
P214
P31
P496
0000-0003-1144-3440
P569
1964-01-01T00:00:00Z
P691
nlk20040146963
P7859
viaf-84855478