Showing results (1-10 of 19) with videos related to
Sort By:
Pageof 2
Bratislavske Lekarske Listy|November 8, 2003
Trisomy 18 mimicking Smith-Lemli-Opitz syndrome in the immediate neonatal periodV Bzduch, D Behulova, L Pevalova, et al.Bratislavske Lekarske Listy|April 1, 2004
Serum free carnitine in medium chain acyl-CoA dehydrogenase deficiencyV Bzduch, D Behulova, A Salingova, et al.Bratislavske Lekarske Listy|January 5, 2002
Metabolic cause of Reye-like syndromeV Bzduch, D Behulova, W Lehnert, et al.Bratislavske Lekarske Listy|January 28, 2017
GAI - distinct genotype and phenotype characteristics in reported Slovak patientsJ Lisyova, R Petrovic, K Jurickova, et al.Bratislavske Lekarske Listy|June 19, 2015
Amount of folic acid in different types of nutrition used in the neonatal periodT Revakova, O Revak, A Vasilenkova, et al.Bratislavske Lekarske Listy|January 7, 2005
A case of Rett syndrome from Ukraine--clinical diagnosis confirmed by mutation analysis of the MECP2 geneV Bzduch, D Zahorakova, E Grechanina, et al.Journal of Bacteriology|December 1, 1990
Recombination at ColE1 cer requires the Escherichia coli xerC gene product, a member of the lambda integrase family of site-specific recombinasesS D Colloms, P Sykora, G Szatmari, et al.Bratislavske Lekarske Listy|February 15, 2013
Intra-abdominal hypertension and acute pancreatitisA Mifkovic, J Skultety, P Sykora, et al.Neoplasma|July 30, 2016
The role of CRP, PCT, IL-6 and presepsin in early diagnosis of bacterial infectious complications in paediatric haemato-oncological patientsM Plesko, J Suvada, M Makohusova, et al.Bratislavske Lekarske Listy|February 23, 2021
Congenital disorders of glycosylation - an umbrella term for rapidly expanding group of rare genetic metabolic disorders - importance of physical investigationD E Lekka, J Brucknerova, A Salingova, et al.Pageof 2