Výsledky vyhľadávania
- 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]
- 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.
- C 526
- 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]