Publikace
- 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
- Mucolipidosis IV: report of a case with ocular restricted phenotype caused by leaky splice mutation2007 | 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
- Degradation of blood group A glycolipid A-6-2 by normal and mutant human skin fibroblasts1998 | 1. lékařská fakulta
- Deffects of glycosphingolipid degradation studied by loading experiments in cultured skin fibroblasts from different lipidoses - experimental approachPublikace 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
- Disturbed angiogenesis in intrauterine growth restriction-compromised placentas at term2018 | 1. lékařská fakulta, Přírodovědecká fakulta
- Specific storage of glycoconjugates with terminal alpha-galactosyl moieties in the exocrine pancreas of Fabry disease patients with blood group B2018 | 1. lékařská fakulta
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