Impact of Type 2 diabetes on Glucokinase diabetes (GCK-MODY) phenotype in a Roma (Gypsy) family - case report von Stanik, J, Kusekova, M, Huckova, M, Valentinova, L, Masindova, I, Stanikova, D, Ferenczova, J, Gasperikova, D, Klimes, I

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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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Systemic scleroderma and Addison's disease von Kosková, E, Rovensky, J, Simorová, E, Kuseková, M

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Pendred syndrome among patients with hypothyroidism: genetic diagnosis, phenotypic variability and occurrence of phenocopies von Banghová, K, Al, Taji E, Novotná, D, Zapletalová, J, Hníková, O, Cáp, J, Klabochová, J, Kúseková, M, Lebl, J

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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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Systemic scleroderma and Addison's disease von Kosková, E, Rovensky, J, Simorová, E, Kuseková, M

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