Výsledky vyhľadávania
- Development of a pattern in biochemical parameters in the core and penumbra during infarct evolution after transient MCAO in rats / Bonová P. ... [et al.] . Neurochemistry International . - Vol. 62, no. 1 (2013), s. 8-14 [Dokument nie je vo fonde knižnice]
- Identification of 11 Novel Homogentisate 1,2 Dioxygenase Variants in Alkaptonuria Patients and Establishment of a Novel LOVD-Based HGD Mutation Database / Zatkova A. ... [et al.] . Journal of inherited metabolic disorders reports . - Vol. 4 (2012), s. 55-65 [Dokument nie je vo fonde knižnice]
- Scheme of Ischaemia-triggered Agents during Brain Infarct Evolution in a Rat Model of Permanent Focal Ischaemia / Bonová P. ... [et al.] . Journal of Molecular Neuroscience . - Vol. 57, no. 1 (2015), s. 73-82 [Dokument nie je vo fonde knižnice]
- Suitability of nitisinone in alkaptonuria 1 (SONIA 1): an international, multicentre, randomised, open-label, no-treatment controlled, parallel-group, dose-response study to investigate the effect of once daily nitisinone on 24-h urinary homogentisic acid excretion in patients with alkaptonuria after 4 weeks of treatment / Ranganath, L. R. ... [et al.] . Annals of the rheumatic diseases . - Vol. 75 (2016), s. 362-367 [Dokument nie je vo fonde knižnice]
- Thirty-nine novel neurofibromatosis 1 (NF1) gene mutations identified in Slovak patients / Nemethova M. ... [et al.] . Annals of Human Genetics . - Vol. 77, no 5 (2013), s. 364–379 [Dokument nie je vo fonde knižnice]
- Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on ‘black bone disease' in Italy / Nemethova M. ... [et al.] . European journal of human genetics . - Vol. 24, no. 1 (2016), s. 66–72 [Dokument nie je vo fonde knižnice]