Daniela Zahorakova

Prague, PR, Czech Republic

Last Updated: 09/26/2026

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Found 9 publications

Analyses of ATP7B mRNA in Nasopharyngeal Swab Samples Increase Yields of Wilson Disease Molecular Genetic Diagnostics.

Analyses of ATP7B mRNA in Nasopharyngeal Swab Samples Increase Yields of Wilson Disease Molecular Genetic Diagnostics.

Journal: Human mutation

Published: August 05, 2025

Enantiomeric separation of bupropion by liquid chromatography on derivatized cyclofructan chiral stationary phase.

Enantiomeric separation of bupropion by liquid chromatography on derivatized cyclofructan chiral stationary phase.

Journal: Chirality

Published: April 26, 2022

Enantioselective separation of zopiclone on immobilized polysaccharide chiral stationary phase by HPLC: Method development and validation.

Enantioselective separation of zopiclone on immobilized polysaccharide chiral stationary phase by HPLC: Method development and validation.

Journal: Journal of pharmaceutical and biomedical analysis

Published: May 22, 2020

Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease.

Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease.

Journal: Clinical genetics

Published: June 07, 2017

Brain iron accumulation in Wilson's disease: A longitudinal imaging case study during anticopper treatment using 7.0T MRI and transcranial sonography.

Brain iron accumulation in Wilson's disease: A longitudinal imaging case study during anticopper treatment using 7.0T MRI and transcranial sonography.

Journal: Journal of magnetic resonance imaging : JMRI

Published: January 15, 2017

Novel CDKL5 Mutations in Czech Patients with Phenotypes of Atypical Rett Syndrome and Early-Onset Epileptic Encephalopathy.

Novel CDKL5 Mutations in Czech Patients with Phenotypes of Atypical Rett Syndrome and Early-Onset Epileptic Encephalopathy.

Journal: Folia biologica

Published: May 18, 2016

MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.

MECP2 mutations in Czech patients with Rett syndrome and Rett-like phenotypes: novel mutations, genotype-phenotype correlations and validation of high-resolution melting analysis for mutation scanning.

Journal: Journal of human genetics

Published: October 12, 2015

Comparison of transcranial sonography-magnetic resonance fusion imaging in Wilson's and early-onset Parkinson's diseases.

Comparison of transcranial sonography-magnetic resonance fusion imaging in Wilson's and early-onset Parkinson's diseases.

Journal: Parkinsonism & related disorders

Published: October 09, 2015

Parkin (PARK 2) mutations are rare in Czech patients with early-onset Parkinson's disease.

Parkin (PARK 2) mutations are rare in Czech patients with early-onset Parkinson's disease.

Journal: PloS one

Published: May 29, 2014

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Last Updated: 09/26/2026