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Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia.
Dolzan V, Sólyom J, Fekete G, Kovács J, Rakosnikova V, Votava F, Lebl J, Pribilincova Z, Baumgartner-Parzer SM, Riedl S, Waldhauser F, Frisch H, Stopar-Obreza M, Krzisnik C, Battelino T. Dolzan V, et al. Among authors: waldhauser f. Eur J Endocrinol. 2005 Jul;153(1):99-106. doi: 10.1530/eje.1.01944. Eur J Endocrinol. 2005. PMID: 15994751
Congenital adrenal hyperplasia: lessons from a multinational study.
Frisch H, Waldhauser F, Lebl J, Solyom J, Hargitai G, Kovacs J, Pribilincova Z, Krzisnik C, Battelino T; MEWPE-CAH Study Group. Frisch H, et al. Among authors: waldhauser f. Horm Res. 2002;57 Suppl 2:95-101. doi: 10.1159/000058109. Horm Res. 2002. PMID: 12065936
Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia.
Votava F, Török D, Kovács J, Möslinger D, Baumgartner-Parzer SM, Sólyom J, Pribilincová Z, Battelino T, Lebl J, Frisch H, Waldhauser F; Middle European Society for Paediatric Endocrinology -- Congenital Adrenal Hyperplasia (MESPE-CAH) Study Group. Votava F, et al. Among authors: waldhauser f. Eur J Endocrinol. 2005 Jun;152(6):869-74. doi: 10.1530/eje.1.01929. Eur J Endocrinol. 2005. PMID: 15941926
Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five middle European countries.
Kovács J, Votava F, Heinze G, Sólyom J, Lebl J, Pribilincová Z, Frisch H, Battelino T, Waldhauser F; Middle European Workshop on Paediatric Endocrinology-Congenital Adrenal Hyperplasia Study Group. Kovács J, et al. Among authors: waldhauser f. J Clin Endocrinol Metab. 2001 Jul;86(7):2958-64. doi: 10.1210/jcem.86.7.7638. J Clin Endocrinol Metab. 2001. PMID: 11443151
93 results