Genetic variants of transferrin in cystic fibrosis von Marklová, E., Albahri, Z., Vaníček, H., Dědek, P., Vališ, M., Kopáčová, M., Vávrová, V.

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Screening for defects in tryptophan metabolism von MARKLOVA, E, MAKOVICKOVA, H, KRAKOROVA, I

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Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin pattern von 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.

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Metabolism of tryptophan in the liver: interference with decarboxylation of other aromatic amino acids von Drsata, J, Marklová, E

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High-performance liquid chromatographic profiling of indolylacryloylglycine and its possible precursors in body fluids von Marklová, Eliška, Fojtášková, Alena

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Hypoglycosylation and disease modifying polymorphism in cystic fibrosis von Marklova, E, Albahri, Z, Vanicek, H, Vavrova, V, Sedlak, V, Ali, A.M

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CDG : a new case of a combined defect in the biosynthesis of N- and O-glycans von ALBAHRI, Ziad, MARKLOVA, Eliska, DEDEK, Petr, HOJDIKOVA, Helena, FIEDLER, Zdenek, LEFEBER, Dirk, WEVERS, Ron A, MORAVA, Eva, WOPEREIS, Suzan

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A method for the estimation of indolylacryloylglycine in urine von Marklová, E., Hais, I.M.

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Chromatographic behaviour of some indole acids on a sephadex column in water and in the presence of salts von Marklová, E., Hais, I.M.

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A new case of 3‐hydroxy‐3‐methylglutaryl‐coenzyme A lyase deficiency von Marklová, E., Verner, P., Pehal, F., Brátová, M., Polák, J.

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