Czech-Slovak Pediatrics - Issue 2/2018
Original Papers
72
79
Urinary iodine concentrations of pregnant women before delivery
D. Neumann, K. Krylová, J. Kulička, A. Jahodová Berková, R. Bílek, M. Kacerovský, M. Bayer
84
Phenylketonuria: Inovative therapy with sapropterin
R. Pazdírková, J. Komárková, M. Hedelová, J. David
Case Report
90
ACTH dependent Cushing´s syndrome – case report
J. Lhotská, J. David, F. Votava, M. Kršek
95
21-hydroxylase deficiency with p.I173N//CYP21A1P/CYP21A2 chimeric gene genotype before and after neonatal screening introduction
D. Novotná, H. Vinohradská, Z. Hrubá
100
New genetic causes of primary adrenal insufficiency
R. Pomahačová, J. Sýkora, J. Zamboryová, P. Paterová, J. Dort, E. Dortová, I. Šubrt
Review
104
Monogenic form of autoimmune diabetes as a part of dysregulation of immune system
V. Straková, P. Dušátková, L. Elblová, Š. Průhová
110
Growth plate disorders causing familiar short stature
L. Plachý, D. Zemková, Š. Průhová, J. Lebl
Czech-Slovak Pediatrics
2018 Issue 2
Most read in this issue
- Growth plate disorders causing familiar short stature
- Thyroglobulin and other laboratory diagnosis parameters in treating hypothyroidism in children
- ACTH dependent Cushing´s syndrome – case report
- Phenylketonuria: Inovative therapy with sapropterin