Inherited metabolic disorders of glycoconjugate metabolism
Pakanova, Z, Nemcovic, M, Ziburova, J, Mucha, J, Salingova, A, Sebova, C, Jurickova, K, Barath, P
Published in Bratislavské lékarské listy (2020)
Published in Bratislavské lékarské listy (2020)
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Congenital disorders of glycosylation - an umbrella term for rapidly expanding group of rare genetic metabolic disorders - importance of physical investigation
Lekka, D E, Brucknerova, J, Salingova, A, Sebova, C, Ostrozlikova, M, Ziburova, J, Nemcovic, M, Sestak, S, Bellova, J, Pakanova, Z, Sivakova, B, Skoknova, M, Bzduch, V, Mucha, J, Barath, P, Brucknerova, I
Published in Bratislavské lékarské listy (2021)
Published in Bratislavské lékarské listy (2021)
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Serum free carnitine in medium chain acyl-CoA dehydrogenase deficiency
Bzduch, V, Behulova, D, Salingova, A, Ponec, J, Fabriciova, K, Kozak, L
Published in Bratislavské lékarské listy (2003)
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Published in Bratislavské lékarské listy (2003)
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Metabolic cause of Reye-like syndrome
Bzduch, V, Behulova, D, Lehnert, W, Fabriciova, K, Kozak, L, Salingova, A, Hrabincova, E, Benedekova, M
Published in Bratislavské lékarské listy (2001)
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Published in Bratislavské lékarské listy (2001)
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Elevated serum biotinidase activity: a new view in diagnostics of hepatic glycogenoses
Holesova, D., Behulova, D., Salingova, A., Ostrozlikova, M., Sebova, C., Fabriciova, K., Bzduch, V., Hlavata, A.
Published in Clinical biochemistry (01.05.2011)
Published in Clinical biochemistry (01.05.2011)
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Rare disease day, conference 29.2.2012 - Poster Session
Published in Acta Facultatis Pharmaceuticae Universitatis Comenianae
(01.01.2012)
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