- An enzymatic glycosylation of nucleoside analogues using β-galactosidase from Escherichia coli2012 | Central Library of Charles University
- Induction and characterization of an unusual alpha-D-galactosidase from Talaromyces flavus2007 | Faculty of Science
- Mutagenesis of Catalytic Nucleophile of beta-Galactosidase Retains Residual Hydrolytic Activity and Affords a Transgalactosidase2021 | Faculty of Science, Central Library of Charles University
- The α-galactosidase type A gene aglA from Aspergillus niger encodes a fully functional α-N-acetylgalactosaminidase2010 | Faculty of Science
- Replacement of alpha-galactosidase A in Fabry disease: effect on fibroblast cultures compared with biopsied tissues of treated patients2008 | First Faculty of Medicine
- Expression of beta-galactosidase and beta-xylosidase genes during microspore and pollen development2005 | Faculty of Science
- Undiscovered lysosomal β-galactosidase deficiency in the patient suffering from spondyloepimetaphyseal dysplasia +1Publication without faculty affiliation
- Fabry Disease: Nine New Mutations in alpha-Galactosidase A Gene and Molecular Carrier Detection2001 | First Faculty of Medicine
- Fabry Disease: Ten New Mutations in alpha-Galactosidase A Gene and Molecular Carrier DetectionPublication without faculty affiliation
- GM1 Gangliosidosis and Morquio B Disease: Expression Analysis of Missense Mutations Affecting the Catalytic Site of Acid beta-Galactosidase2009 | First Faculty of Medicine
- Fabry disease - Vascular manifestations2010 | First Faculty of Medicine
- Recurrence of Fabry disease as a result of paternal germline mosaicism for alpha-galactosidase A gene mutation2005 | First Faculty of Medicine
- Blood group B glycosphingolipids in alpha-galactosidase deficiency /Fabry disease/ - influence of secretor status1997 | Faculty of Physical Education and Sport
- Replacement of alpha-galactosidase A in Fabry disease: effect on fibroblast cultures compared with biopsied tissues of treated patients2008 | Publication without faculty affiliation
- Biochemistry of Fabry Disease2010 | First Faculty of Medicine
- Estrogenic and androgenic activity of PCBs, their chlorinated metabolites and other endocrine disruptors estimated with two in vitro yeast assays2009 | Faculty of Science
- Characterization of gana-I, a Caenorhabditis elegans gene encoding a single ortholog of vertebrate alpha-galactosidase and alpha-N-acetylgalactosaminidase2005 | First Faculty of Medicine
- Relationship between X-inactivation and clinical involvement in Fabry heterozygotes. Eleven novel mutations in the alpha-galactosidase A gene in the Czech and Slovak population2005 | First Faculty of Medicine
- Fabry disease - Vascular manifestations2010 | Third Faculty of Medicine
- The coincidence of IgA nephropathy and Fabry disease2013 | First Faculty of Medicine, Faculty of Physical Education and Sport
- Prevalence of Fabry disease in men with tinnitus and sensorineural hearing loss2021 | First Faculty of Medicine, Third Faculty of Medicine
- Fabry disease - more common than you think2011 | First Faculty of Medicine
- Fabry disease - an overview for a dermatologist2017 | First Faculty of Medicine
- Evaluation of a low dose, after a standard therapeutic dose, of agalsidase beta during enzyme replacement therapy in patients with Fabry disease2009 | First Faculty of Medicine
- Detection of infant faecal bifidobacteria by enzymatic methods2005 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data2009 | First Faculty of Medicine
- Fabry's disease from the point of view of nephrology2015 | First Faculty of Medicine
- Time to treatment benefit for adult patients with Fabry disease receiving agalsidase beta: Data from the Fabry Registry2016 | First Faculty of Medicine
- Comparison of bacterial flora and enzymatic activity in faeces of infants and calves2006 | Second Faculty of Medicine