B. Petrák

A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17

Markéta Havlovičová, Drahuše Novotná, Eduard Kočárek et al. · American Journal of Medical Genetics Part A · 2006 · 93 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Homozygous<b><i>EXOSC3</i></b>Mutation c.92G→C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma

Jaroslava Paulasová Schwabová, Dana Šafka Brožková, B. Petrák et al. · Journal of Neurogenetics · 2013 · 45 citations

Life Sciences, Genetics, Molecular Genetics +14

Brain gliomas, hydrocephalus and idiopathic aqueduct stenosis in children with neurofibromatosis type 1

Marie Glombová, B. Petrák, Jiří Lisý et al. · Brain and Development · 2019 · 28 citations

Medicine, Neuroscience, Pediatrics +16

The importance of advanced parental age in the origin of neurofibromatosis type 1

Marta Šnajderová, Vincent M. Riccardi, B. Petrák et al. · American Journal of Medical Genetics Part A · 2012 · 27 citations

Life Sciences, Genetics, Pediatrics +15

Early predictors of clinical and mental outcome in tuberous sclerosis complex: A prospective study

Barbora Beňová, B. Petrák, Martin Kynčl et al. · European Journal of Paediatric Neurology · 2018 · 27 citations

Medicine, Neurology, Psychiatry +2