- Gitelman Syndrome as a Cause of Psychomotor Retardation in a Toddler2013 | First Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Gastroesophageal reflux disease in children with psychomotor retardation (PMR)2016 | Second Faculty of Medicine
- Vitamin B 12 deficiency in breastfed infants-treatable cause of psychomotor retardation: etiology, clinical signs and laboratory findings2008 | First Faculty of Medicine
- Surgical Gastrostomy in Children2003 | Second Faculty of Medicine
- Disorder of Growth and Development in a Boy with X-bound Ichthyosis, Protracted Delivery and Low Level of Estriol in the Mother during Pregnancy2009 | First Faculty of Medicine
- Adenylosuccinate lyase deficiency in a Czech girl and two siblings1994 | Second Faculty of Medicine
- Disorder of Growth and Development in a Boy with X-bound Ichthyosis, Protracted Delivery and Low Level of Estriol in the Mother during Pregnancy2009 | Second Faculty of Medicine
- Early Diagnosis of the Chromosomal Deletion 5q14.2-q21.3 in a Preterm Newborn: Case Report2013 | First Faculty of Medicine
- Clinical, biochemical and molecular findings in seven Polish patients with adenylosuccinate lyase deficiency2008 | First Faculty of Medicine
- Psychomotor stimulation by aquatics2002 | Publication without faculty affiliation
- Clinical and Molecular Analyses in Eight Children with Congenital Disorders of Glycosylation2003 | First Faculty of Medicine
- Short Communication.Abnormalities in succinylpurines in fumarase deficiency: Possible role in pathogenesis of CNS impairment.2000 | Faculty of Physical Education and Sport
- Fahr's Syndrome: Pseudohypoparathyroidism Type Ib Masquerading as Epileptic Seizures2022 | Faculty of Medicine in Hradec Králové
- Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures2011 | Faculty of Science, First Faculty of Medicine
- Different laboratory and muscle biopsy findings in a family with an m.8851T > C mutation in the mitochondrial MTATP6 gene2013 | First Faculty of Medicine, Second Faculty of Medicine
- Amisulprid in dysthymia and anxiety disorders - resources and case reports2004 | First Faculty of Medicine
- Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures2011 | First Faculty of Medicine
- CDG: a new case of a combined defect in the biosynthesis of N- and O-glycans2006 | Faculty of Medicine in Hradec Králové, Central Library of Charles University
- Problems of ELBW neonates during the period of adolescence and adulthood2007 | Third Faculty of Medicine
- Adenylosuccinate lyase deficiency2015 | First Faculty of Medicine
- Bobble-head doll syndrome: therapeutic outcome and long-term follow-up in four children2012 | First Faculty of Medicine
- Bobble-head doll syndrome: therapeutic outcome and long-term follow-up in four children2012 | Second Faculty of Medicine
- Different causes of reduced sensitivity to thyroid hormone: Diagnosis and clinical management2014 | First Faculty of Medicine
- Two Different Causes of Paediatric Hypercalcaemia2018 | Central Library of Charles University
- Case report of patients with a marker chromosome2004 | Second Faculty of Medicine
- Mitochondrial DNA depletion in Alpers syndrome2004 | Second Faculty of Medicine
- Metabolites of De Novo Purine Synthesis: Metabolic Regulators and Cytotoxic Compounds2022 | First Faculty of Medicine
- Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency2012 | First Faculty of Medicine
- Genotype phenotype spectrum of PYCR1-related autosomal recessive cutis laxa2013 | Second Faculty of Medicine
- Novel Splicing Variant in the PMM2 Gene in a Patient With PMM2-CDG Syndrome Presenting With Pericardial Effusion: A Case Report2020 | First Faculty of Medicine