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Czech-Slovak Pediatrics - Issue 2/2018
Original Papers
7279Urinary iodine concentrations of pregnant women before deliveryD. Neumann, K. Krylová, J. Kulička, A. Jahodová Berková, R. Bílek, M. Kacerovský, M. Bayer
84Phenylketonuria: Inovative therapy with sapropterinR. Pazdírková, J. Komárková, M. Hedelová, J. David
Case Report
90ACTH dependent Cushing´s syndrome – case reportJ. Lhotská, J. David, F. Votava, M. Kršek
9521-hydroxylase deficiency with p.I173N//CYP21A1P/CYP21A2 chimeric gene genotype before and after neonatal screening introductionD. Novotná, H. Vinohradská, Z. Hrubá
100New genetic causes of primary adrenal insufficiencyR. Pomahačová, J. Sýkora, J. Zamboryová, P. Paterová, J. Dort, E. Dortová, I. Šubrt
Review
104Monogenic form of autoimmune diabetes as a part of dysregulation of immune systemV. Straková, P. Dušátková, L. Elblová, Š. Průhová
110Growth plate disorders causing familiar short statureL. 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
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