Julia Stellmachova
Olomouc, Czech Republic
Last Updated: 09/26/2026
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Found 9 publications
Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.
Journal: Diagnostics (Basel, Switzerland)
Published: March 21, 2022
SPG11: clinical and genetic features of seven Czech patients and literature review.
Journal: Neurological research
Published: March 07, 2022
High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic.
Journal: Life (Basel, Switzerland)
Published: December 21, 2021
Whole Exome Sequencing Study in Isolated South-Eastern Moravia (Czechia) Population Indicates Heterogenous Genetic Background for Parkinsonism Development.
Journal: Frontiers in neuroscience
Published: November 18, 2021
Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms.
Journal: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia
Published: October 01, 2020
Searching for genetic variants associated with thrombophilia.
Journal: Casopis lekaru ceskych
Published: May 03, 2019
Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found.
Journal: Neuroscience letters
Published: March 27, 2019
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Last Updated: 09/26/2026