Publikace
- Specific storage of glycoconjugates with terminal alpha-galactosyl moieties in the exocrine pancreas of Fabry disease patients with blood group B2018 | 1. lékařská fakulta
- Fabry disease: renal sphingolipid distribution in the alpha-Gal A knockout mouse model by mass spectrometric and immunohistochemical imaging2015 | 1. lékařská fakulta
- Náhrada alfa-galktosidasy A u Fabryho nemoci: porovnání účinku enzymu v kulturách fibroblastů a v bioptických tkáních léčených pacientů2008 | 1. lékařská fakulta
- Prosaposin Deficiency - a Rarely Diagnosed, Rapidly Progressing, Neonatal Neurovisceral Lipid Storage Disease. Report of a Further Patient2005 | 1. lékařská fakulta
- Defects in degradation of blood group A and B glycosphingolipids in Schindler and Fabry diseases2002 | 1. lékařská fakulta
- Undiscovered lysosomal β-galactosidase deficiency in the patient suffering from spondyloepimetaphyseal dysplasiaPublikace bez příslušnosti k fakultě
- AGAL misprocessing-induced ER stress and the unfolded protein response: lysosomal storage-independent mechanism of Fabry disease pathogenesis?2022 | 1. lékařská fakulta, 3. lékařská fakulta
- Loading of cell cultures with cholesterol-dextran particles as a new functional test for Niemann-Pick type C disease2022 | 1. lékařská fakulta
- Transcript, protein, metabolite and cellular studies in skin fibroblasts demonstrate variable pathogenic impacts of NPC1 mutations2020 | 1. lékařská fakulta
- Disturbed angiogenesis in intrauterine growth restriction-compromised placentas at term2018 | 1. lékařská fakulta, Přírodovědecká fakulta
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