Borivoj Petrak - Publications

Efficacy of first line of bevacizumab in patients with neurofibromatosis 2-related vestibular schwannomas.

Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery

Published: May 08, 2025

Vigabatrin-associated brain magnetic resonance imaging abnormalities and clinical symptoms in infants with tuberous sclerosis complex.

Journal: Epilepsia

Published: August 16, 2024

Significance of the Absence of Focal Areas of Signal Intensity on Brain Magnetic Resonance Imaging Examinations in Legius Syndrome.

Journal: Pediatric neurology

Published: May 24, 2024

Molecular EPISTOP, a comprehensive multi-omic analysis of blood from Tuberous Sclerosis Complex infants age birth to two years.

Journal: Nature communications

Published: February 23, 2023

miRNAs and isomiRs: Serum-Based Biomarkers for the Development of Intellectual Disability and Autism Spectrum Disorder in Tuberous Sclerosis Complex.

Journal: Biomedicines

Published: June 24, 2022

Torcular dural sinus malformations: a grading system proposal.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: December 13, 2019

Torcular dural sinus malformations: a single-center case series and a review of literature.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: May 14, 2019

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

Journal: Brain & development

Published: September 29, 2018

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

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: February 28, 2017

EFFECTS: an expanded access program of everolimus for patients with subependymal giant cell astrocytoma associated with tuberous sclerosis complex.

Journal: BMC neurology

Published: January 07, 2016

Neurofibromatosis von Recklinghausen type 1 (NF1) - clinical picture and molecular-genetics diagnostic

Journal: Ceskoslovenska patologie

Published: February 12, 2015

Homozygous EXOSC3 mutation c.92G→C, p.G31A is a founder mutation causing severe pontocerebellar hypoplasia type 1 among the Czech Roma.

Journal: Journal of neurogenetics

Published: July 26, 2013