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Twenty years of newborn screening for congenital adrenal hyperplasia and congenital primary hypothyroidism: experiences from the DGKED/AQUAPE study group for quality improvement in... by Hammersen, Johanna (Author) , Bettendorf, Markus (Author) , Bonfig, Walter (Author) , Schönau, Eckhard (Author) , Warncke, Katharina (Author) , Eckert, Alexander J. (Author) , Fricke-Otto, Susanne (Author) , Palm, Katja (Author) , Holl, Reinhard W. (Author) , Wölfle, Joachim (Author) ,

• Resolving-System, kostenfrei
• Verlag, lizenzpflichtig, Volltext

Typical characteristics of children with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: a single-centre experience and review of the literature by Breil, Thomas (Author) , Yakovenko, Vira (Author) , Inta, Ioana (Author) , Choukair, Daniela (Author) , Klose, Daniela (Author) , Mittnacht, Janna (Author) , Alrajab, Abdulsattar (Author) , Grulich-Henn, Jürgen (Author) , Bettendorf, Markus (Author) ,

• Verlag, Volltext
• Verlag, Volltext