Publications
- Transient Hyperphosphatasemia in a Child with Autism Spectrum Disorder2022 | First Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Pilsen
- Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study2022 | First Faculty of Medicine
- Changes in Transcription Pattern Lead to a Marked Decrease in COX, CS and SQR Activity After the Developmental Point of the 22nd Gestational Week2018 | First Faculty of Medicine
- Clinical and biochemical characteristics of Kawasaki syndrome in 22 children2014 | First Faculty of Medicine
- Children's Ophthalmology2022 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University, Faculty of Medicine in Pilsen, Faculty of Education, Faculty of Medicine in Hradec Králové
- Metabolic myopathies2022 | First Faculty of Medicine
- DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome2022 | First Faculty of Medicine
- Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databases2022 | First Faculty of Medicine
- A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syndrome2022 | First Faculty of Medicine
- Subjective and polysomnographic evaluation of sleep in mitochondrial optic neuropathies2021 | First Faculty of Medicine
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