- 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 | Second Faculty of Medicine
- Congenital disorders of glycosylation (CDG Syndrome) in fourteen children with psychomotor delay, hypotonia, strabismus and other various organ involvementPublication without faculty affiliation
- Clinical and Molecular Analyses in Eight Children with Congenital Disorders of Glycosylation2003 | First Faculty of Medicine
- Nutritional deficit of vitamin B12 in infants2009 | First 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
- Amisulprid in dysthymia and anxiety disorders - resources and case reports2004 | First Faculty of Medicine
- Bilateral schizencephaly in a preterm newborn2020 | Second Faculty of Medicine, Third Faculty of Medicine, Central Library of Charles University
- Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures2011 | First Faculty of Medicine
- Clinical presentation and metabolic consequences in 40 breastfed infants with nutritional vitamin B-12 deficiency - What have we learned?2010 | First Faculty of Medicine
- Problems of ELBW neonates during the period of adolescence and adulthood2007 | Third Faculty of Medicine
- Bobble-head doll syndrome: therapeutic outcome and long-term follow-up in four children2012 | First Faculty of Medicine
- Novel Mutations in the Tyrosine Hydroxylase Gene in the First Czech Patient with Tyrosine Hydroxylase Deficiency2012 | First Faculty of Medicine
- Case report of patients with a marker chromosome2004 | Second Faculty of Medicine
- Congenital and postnatal cytomegalovirus infections2022 | Second Faculty of Medicine
- Neonatal Diabetes Mellitus Caused by Activation Mutation in the Gene Encoding the Kir6.2 Subunit of Potassium Channel: Is Insulindependency Inevitably Life-long?2005 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Physical Education and Sport
- Pelizaeus Merzbacher's disease (PMD) - Detection of the most frequent mutation of the proteolipid protein gene in Czech patients and families with the classical form of PAID2003 | First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport