Genetic variants of transferrin in cystic fibrosis
Marklová, E., Albahri, Z., Vaníček, H., Dědek, P., Vališ, M., Kopáčová, M., Vávrová, V.
Published in Journal of inherited metabolic disease (01.06.2008)
Published in Journal of inherited metabolic disease (01.06.2008)
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Genetic variants of transferrin in the diagnosis of protein hypoglycosylation
Albahri, Z., Marklová, E., Vaníček, H., Minxová, L., Dédek, P., Skálová, S.
Published in Journal of inherited metabolic disease (01.12.2005)
Published in Journal of inherited metabolic disease (01.12.2005)
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Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern
Mohamed, M., Guillard, M., Wortmann, S.B., Cirak, S., Marklova, E., Michelakakis, H., Korsch, E., Adamowicz, M., Koletzko, B., van Spronsen, F.J., Niezen-Koning, K.E., Matthijs, G., Gardeitchik, T., Kouwenberg, D., Lim, B. Chan, Zeevaert, R., Wevers, R.A., Lefeber, D.J., Morava, E.
Published in Biochimica et biophysica acta (01.06.2011)
Published in Biochimica et biophysica acta (01.06.2011)
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Hypoglycosylation and disease modifying polymorphism in cystic fibrosis
Marklova, E, Albahri, Z, Vanicek, H, Vavrova, V, Sedlak, V, Ali, A.M
Published in Journal of cystic fibrosis (01.06.2008)
Published in Journal of cystic fibrosis (01.06.2008)
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Screening for organic acid disorders
Marklová, E, Brátová, M, Vorísek, V
Published in Acta medica Lékarskí fakulty Univerzity Karlovy v Hradci Králove (1997)
Published in Acta medica Lékarskí fakulty Univerzity Karlovy v Hradci Králove (1997)
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The role of TLC in the screening of inherited metabolic diseases
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Conference Proceeding
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A new case of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency
Marklová, E, Verner, P, Pehal, F, Brátová, M, Polák, J
Published in Journal of inherited metabolic disease (01.12.1987)
Published in Journal of inherited metabolic disease (01.12.1987)
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