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A Novel MTTK Gene Variant m.8315A>C as a Cause of MERRF Syndrome.
Štufková H, Kolářová H, Lokvencová K, Honzík T, Zeman J, Hansíková H, Tesařová M. Štufková H, et al. Among authors: kolarova h. Genes (Basel). 2022 Jul 14;13(7):1245. doi: 10.3390/genes13071245. Genes (Basel). 2022. PMID: 35886028 Free PMC article.
Human Alveolar Echinococcosis, Czech Republic, 2007-2014.
Kolářová L, Matějů J, Hrdý J, Kolářová H, Hozáková L, Žampachová V, Auer H, Stejskal F. Kolářová L, et al. Among authors: kolarova h. Emerg Infect Dis. 2015 Dec;21(12):2263-5. doi: 10.3201/eid2112.150743. Emerg Infect Dis. 2015. PMID: 26583699 Free PMC article. No abstract available.
Clinical manifestation of mitochondrial diseases.
Magner M, Kolářová H, Honzik T, Švandová I, Zeman J. Magner M, et al. Among authors: kolarova h. Dev Period Med. 2015 Oct-Dec;19(4):441-9. Dev Period Med. 2015. PMID: 26982751 Review.
The phenotypic spectrum of fifty Czech m.3243A>G carriers.
Dvorakova V, Kolarova H, Magner M, Tesarova M, Hansikova H, Zeman J, Honzik T. Dvorakova V, et al. Among authors: kolarova h. Mol Genet Metab. 2016 Aug;118(4):288-95. doi: 10.1016/j.ymgme.2016.06.003. Epub 2016 Jun 6. Mol Genet Metab. 2016. PMID: 27296531
131 results