- Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations2009 | First Faculty of Medicine
- Rare PSAP Variants and Possible Interaction with GBA in REM Sleep Behavior Disorder2022 | First Faculty of Medicine
- Tubulo-squamous polyp of the vagina2015 | Faculty of Medicine in Hradec Králové
- Prosaposin Deficiency - a Rarely Diagnosed, Rapidly Progressing, Neonatal Neurovisceral Lipid Storage Disease. Report of a Further Patient2005 | First Faculty of Medicine
- Vaginal myofibroblastoma with glands expressing mammary and prostatic antigens2012 | Faculty of Medicine in Pilsen
