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  1. 1.Case study: monitoring of Glc4 tetrasaccharide in the urine of Pompe patients, use of MALDI-TOF MS, and 1H NMR

    Case study: monitoring of Glc4 tetrasaccharide in the urine of Pompe patients, use of MALDI-TOF MS, and 1H NMR  / Pakanova Z., Matulova M., Uhliarikova I. et al. .  Chemical Papers . - Volume 73, pages701–711(2019)   [Dokument nie je vo fonde knižnice]
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  2. 2.Congenital disorders of glycosylation - an umbrella term for rapidly expanding group of rare genetic metabolic disorders - importance of physical investigation

    Congenital disorders of glycosylation - an umbrella term for rapidly expanding group of rare genetic metabolic disorders - importance of physical investigation  / Lekka D.E. ... [et al.] .  Bratislavské lekárske listy : international journal for biomedical sciences and clinical medicine. - ISSN 0006-9248 . - Vol. 122, no. 3 (2021), s. 190-195  : ilustr., fareb. fotogr., schémy, tab.  
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  3. 3.Molecular diagnosis of Pompe disease using MALDI TOF/TOF and 1H NMR

    Molecular diagnosis of Pompe disease using MALDI TOF/TOF and 1H NMR  / Pakanová Z. ... [et al.] .  Chemical papers . - Vol. 70, no. 3 (2016), s. 265-271   [Dokument nie je vo fonde knižnice]
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