Hana Kolarova
Prague, PR 12808, Czech Republic
Last Updated: 09/26/2026
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Found 22 publications
Transient Hyperphosphatasemia in a Child with Autism Spectrum Disorder.
Journal: Acta medica (Hradec Kralove)
Published: July 06, 2022
A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syndrome
Journal: Genes
Published: June 01, 2022
Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study.
Journal: Orphanet journal of rare diseases
Published: March 07, 2022
Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databases.
Journal: EBioMedicine
Published: October 18, 2021
DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome.
Journal: Brain : a journal of neurology
Published: October 18, 2021
Comparison of methods used for evaluation of mutagenicity/genotoxicity of model chemicals - parabens.
Journal: Physiological research
Published: March 01, 2021
The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions.
Journal: Brain sciences
Published: September 15, 2020
Subjective and polysomnographic evaluation of sleep in mitochondrial optic neuropathies.
Journal: Journal of sleep research
Published: January 14, 2020
Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I.
Journal: BMC pediatrics
Published: August 27, 2019
Charles Bonnet syndrome in Leber's hereditary optic neuropathy.
Journal: Journal of neurology
Published: August 27, 2018
Changes in transcription pattern lead to a marked decrease in COX, CS and SQR activity after the developmental point of the 22(nd) gestational week.
Journal: Physiological research
Published: November 16, 2017
Peripapillary microcirculation in Leber hereditary optic neuropathy.
Journal: Acta ophthalmologica
Published: October 03, 2017
Last Updated: 09/26/2026