Eliska Marklová
Department of Pediatrics
Charles University in Prague
Faculty of Medicine and University Hospital
Hradec Králové
Czech Republic
Name/email consistency: high
- Amniotic fluid α-fetoprotein microheterogeneity in the prenatal diagnosis of congenital disorders of glycosylation type Ia. Marklová, E., Albahri, Z. Clin. Chem. Lab. Med. (2010)
- Transferrin D protein variants in the diagnosis of congenital disorders of glycosylation (CDG). Marklová, E., Albahri, Z. J. Clin. Lab. Anal. (2009)
- Genetic variants of transferrin in cystic fibrosis. Marklová, E., Albahri, Z., Vanícek, H., Dedek, P., Valis, M., Kopácová, M., Vávrová, V. J. Inherit. Metab. Dis. (2008)
- Screening and diagnosis of congenital disorders of glycosylation. Marklová, E., Albahri, Z. Clin. Chim. Acta (2007)
- Inflammation and genes. Marklová, E. Acta. Medica. (Hradec. Kralove) (2007)
- Pitfalls and drawbacks in screening of congenital disorders of glycosylation. Marklová, E., Albahri, Z. Clin. Chem. Lab. Med. (2004)
- HPLC profiling of Trp-related metabolites in humans. Marklová, E., Albahri, Z., Nozicková, M. Adv. Exp. Med. Biol. (2003)
- Microelements and inherited metabolic diseases. Marklová, E. Acta. Medica. (Hradec. Kralove) (2002)
- Genetic aspects of diabetes mellitus. Marklová, E. Acta. Medica. (Hradec. Kralove) (2001)
- Screening for defects in tryptophan metabolism. Marklová, E., Makovicková, H., Krákorová, I. J. Chromatogr. A (2000)
- Where does indolylacrylic acid come from?. Marklová, E. Amino. Acids (1999)
