Two novel mutations in seven Czech and Slovak kindreds with familial neurohypophyseal diabetes insipidus—benefit of genetic testing von Hrčková, Gabriela, Jankó, Viktor, Kytnarová, Jitka, Čižmárová, Michaela, Tesařová, Markéta, Košťálová, Ľudmila, Virgová, Daniela, Dallos, Tomáš, Hána, Václav, Lebl, Jan, Zeman, Jiří, Kovács, László

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Isoelectric Focusing of Serum Apolipoprotein C-III as a Sensitive Screening Method for the Detection of O-glycosylation Disturbances von Ondrušková, Nina, Honzík, Tomáš, Kytnarová, Jitka, Matoulek, Martin, Zeman, Jiří, Hansíková, Hana

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Post-natal growth of 157 children born as extremely premature neonates von Jitka, Kytnarova, Blanka, Zlatohlavková, Ales, Kubena, Daniela, Markova, Milena, Dokoupilova, Richard, Plavka, Jiri, Zeman

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High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism von Rozenkova, Klara, Malikova, Jana, Nessa, Azizun, Dusatkova, Lenka, Bjørkhaug, Lise, Obermannova, Barbora, Dusatkova, Petra, Kytnarova, Jitka, Aukrust, Ingvild, Najmi, Laeya A, Rypackova, Blanka, Sumnik, Zdenek, Lebl, Jan, Njølstad, Pål R, Hussain, Khalid, Pruhova, Stepanka

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Cytosine-Adenosine (CA)n repeats polymorphism in IGF-I gene and early growth in infants born appropriate and small for gestational age von Kytnarova, Jitka, Vesela, Katerina, Zlatohlavkova, Blanka, Dohnalova, Alena, Fedorova, Maria, Krsek, Michal, Zeman, Jiri

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