Publications
- Neurofibromatosis von Recklinghausen type I (NF1) - clinical picture in childhood, diagnosis and therapy2023 | Second Faculty of Medicine
- Monozygotic twins with Legius syndrome and differential diagnosis of Legius syndrome and neurof bromatosis type 12021 | Second Faculty of Medicine
- Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 12019 | Second Faculty of Medicine
- Neurofibromatosis von Recklinghausen type 1 (NF1) - the most common neurocutaneous disorder2018 | Second Faculty of Medicine
- Genotype/phenotype correlation in Czech tuberous sclerosis patients2016 | Second Faculty of Medicine
- Neurofibromatosis von Recklinghausen type 1 (NF1) - clinical picture and molecular-genetics diagnostic2015 | First Faculty of Medicine, Second Faculty of Medicine
- Neurofibromatosis from the view of dermatologist2015 | Second Faculty of Medicine
- Tuberous Sclerosis Complex in children followed from neonatal period for prenatally diagnosed cardiac rhabdomyoma - two case reports2013 | First Faculty of Medicine, Faculty of Physical Education and Sport, Second Faculty of Medicine
- Homozygous EXOSC3 Mutation c.92G -> C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma2013 | Second Faculty of Medicine
- Idiopathic Aqueductal Stenosis and Developmental Speech Disorder in Children with Neurofibromatosis von Recklinghausen type 1-Two Case Reports2012 | Second Faculty of Medicine
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