Publications
- Metabolic adaptation of human skin fibroblasts to ER stress caused by glycosylation defect in PMM2-CDG2023 | First Faculty of Medicine
- Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington's disease2022 | First Faculty of Medicine
- Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control2021 | First Faculty of Medicine, Faculty of Science, Second Faculty of Medicine
- Buccal epithelial cells as potential non-invasive materials for the monitoring of mitochondrial disturbances to track Huntington's disease progression : a pilot study2015 | First Faculty of Medicine
- Acyl-CoA binding domain containing 3 (ACBD3) protein in Huntington's disease human skin fibroblasts2015 | First Faculty of Medicine
- Non-invasive screening of cytochrome c Oxidase Deficiency in Children Using a Dipstick Immunocapture Assay2014 | First Faculty of Medicine
- Mitochondrial Dysfunction in a High Intraocular Pressure-Induced Retinal Ischemia Minipig Model2022 | First Faculty of Medicine, Faculty of Science
- Knock-Out of ACBD3 Leads to Dispersed Golgi Structure, but Unaffected Mitochondrial Functions in HEK293 and HeLa Cells2021 | First Faculty of Medicine
- Isolation and Characterization of Small Extracellular Vesicles from Porcine Blood Plasma, Cerebrospinal Fluid, and Seminal Plasma2019 | First Faculty of Medicine
- Deterioration of mitochondrial bioenergetics and ultrastructure impairment in skeletal muscle of a transgenic minipig model in the early stages of Huntington's disease2019 | First Faculty of Medicine
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