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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Transient hyperphosphatasemia in pediatric renal transplant patients — Is there a need for concern?
Skalova, S, Kutilek, S, Vethamuthu, J, Aborawi, A, Geier, P, Feber, J
Published in Bone (New York, N.Y.) (01.07.2009)
Published in Bone (New York, N.Y.) (01.07.2009)
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Journal Article
Intracardiac thrombus--a rare complication of the steroid resistant nephrotic syndrome
Skalova, S, Lukes, A, Vanicek, H, Klein, T, Hak, J, Dedek, P, Ocenaskova, E
Published in Bratislavské lékarské listy (2008)
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Published in Bratislavské lékarské listy (2008)
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Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9
Mucha, Bettina, Ozaltin, Fatih, Hinkes, Bernward G, Hasselbacher, Katrin, Ruf, Rainer G, Schultheiss, Michael, Hangan, Daniela, Hoskins, Bethan E, Everding, Anne Schulze, Bogdanovic, Radovan, Seeman, Thomas, Hoppe, Bernd, Hildebrandt, Friedhelm
Published in Pediatric research (01.02.2006)
Published in Pediatric research (01.02.2006)
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Journal Article
Wegener's granulomatosis in a 15-year-old boy
Skálová, Sylva, Minxová, Lenka, Podhola, Miroslav
Published in Turkish journal of pediatrics (01.10.2003)
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Published in Turkish journal of pediatrics (01.10.2003)
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