Classes
Publications
- Rare cause of blindness in patient with nasal polyposis: Lebers hereditary neuropathy of the optic nerve2011 | First Faculty of Medicine
- Histopathological Diagnosis of Mitochondrial Myopathies – Indications and the Utility of Muscle Biopsy2011 | First Faculty of Medicine
- Elevated lactate is a reliable marker pointing to mitochondrial disorders even in children after brief seizures.2010 | First Faculty of Medicine, Faculty of Science, Faculty of Physical Education and Sport
- Biochemical nad molecular characteristics in 11 czech children with tyrosinemia type I2010 | First Faculty of Medicine
- Girl with congenital disorder of glycosylation - case report2009 | First Faculty of Medicine
- Clinical Manifestations and Results of Laboratory Examinations in Four Patients with Alpha-Mannosidosis2008 | First Faculty of Medicine
- Hepatocellular carcinoma in an infant with tyrosinemia type 12023 | First Faculty of Medicine, Second Faculty of Medicine
- Inherited disorders of carbohydrate metabolism2023 | First Faculty of Medicine
- Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes2023 | First Faculty of Medicine
- Autosomal dominant Zellweger spectrum disorder caused by de novo variants in PEX14 gene2023 | First Faculty of Medicine
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