Publications
- Congenital hypomyelination in conjunction with de-novo mutation in the gene for the peripheral myelin protein 22 - the first confirmed case in the CR and review of the literature2002 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport
- An inherited 2q13 deletion in a patient with Marfan syndromePublication without faculty affiliation
- Neonatal case reports2020 | Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
- Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found2020 | Second Faculty of Medicine
- Křeče u donošeného novorozence - kazuistika2019 | Second Faculty of Medicine
- First cases in the Czech Republic of the Hallervorden-Spatz Disease resulting from mutation in the Pantothenate Kinase 2 Gene2005 | Second Faculty of Medicine
- Neonatal morbidity and long-term outcome of infants with intrauterine growth restriction born at tertiary center2004 | Second Faculty of Medicine
- Neonatal moribidity and neuromotor development of infants with intrauterine growth restriction (IUGR)2004 | Second Faculty of Medicine
- IUGR - pathokinesiologie in newborn and suclings +12002 | Second Faculty of Medicine, Central Library of Charles University
- Apallic Syndrome in Children: Development and Prognosis2002 | Second Faculty of Medicine
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