New Mutations Associated with Rasopathies in a Central European Population and Genotype–Phenotype Correlations von Čizmárová, M., Hlinková, K., Bertok, S., Kotnik, P., Duba, H.C., Bertalan, R., Poločková, K., Košťálová, Ľ., Pribilincová, Z., Hlavatá, A., Kovács, L., Ilenčíková, D.

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Role of an interdisciplinary approach in the healing of long bone fractures in patients with osteogenesis imperfecta von Kokavec, M, Novorolský, K, Pribilincová, Z

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Rasopathies - dysmorphic syndromes with short stature and risk of malignancy von Cizmarova, M, Kostalova, L, Pribilincova, Z, Lasabova, Z, Hlavata, A, Kovacs, L, Ilencikova, D

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New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype Correlations: Rasopathies in Central Europe von Čizmárová, M., Hlinková, K., Bertok, S., Kotnik, P., Duba, H.C., Bertalan, R., Poločková, K., Košťálová, Ľ., Pribilincová, Z., Hlavatá, A., Kovács, L., Ilenčíková, D.

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Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five Middle European countries von KOVACS, Jozsef, VOTAVA, Felix, HEINZE, Georg, SOLYOM, Janos, LEBL, Jan, PRIBILINCOVA, Zuzana, FRISCH, Herwig, BATTELINO, Tadej, WALDHAUSER, Franz

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Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia von Dolž, an, 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, Krž, išnik, C, Battelino, T

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Late onset of familial neurogenic diabetes insipidus in monozygotic twins von Cizmarova, M, Nagyova, G, Janko, V, Pribilincova, Z, Virgova, D, Ilencikova, D, Kovacs, L

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Growth patterns and final height in congenital adrenal hyperplasia due to classical 21-hydroxylase deficiency. Results of a multicenter study von Hargitai, G, Sólyom, J, Battelino, T, Lebl, J, Pribilincová, Z, Hauspie, R, Kovács, J, Waldhauser, F, Frisch, H

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Problems of metabolic syndrome diagnostics in children von Vitariusova, E, Kostalova, L, Pribilincova, Z, Hlavata, A, Kovacs, L

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Congenital Adrenal Hyperplasia: Lessons from a Multinational Study von Frisch, H., Waldhauser, F., Lebl, J., Solyom, J., Hargitai, G., Kovacs, J., Pribilincova, Z., Krzisnik, C., Battelino, T.

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Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia von Votava, Felix, Török, Dóra, Kovács, József, Möslinger, Dorothea, Baumgartner-Parzer, Sabina M, Sólyom, János, Pribilincová, Zuzana, Battelino, Tadej, Lebl, Jan, Frisch, Herwig, Waldhauser, Franz

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The results of replacement therapy in patients with growth hormone deficiency von Košt'álová, L., Mišiková, ., Bieliková, S., Kúseková, M., Leščišinová, M., Pašková, M., Pribilincová, Z., Šimeková, Z.

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PCR based diagnosis of 21-hydroxylase gene defects in Slovak patients with congenital adrenal hyperplasia von Pinterova, L, Garami, M, Pribilincova, Z, Behulova, R, Mezenska, R, Lukacova, M, Zorad, S

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