Zeman J - Search Results

1

Mitochondrial DNA haplogroups in the Czech population compared to other European countries.

Vidrová V, Tesarová M, Trefilova E, Honzík T, Magner M, Zeman J. Vidrová V, et al. Among authors: zeman j. Hum Biol. 2008 Dec;80(6):669-74. doi: 10.3378/1534-6617-80.6.669. Hum Biol. 2008. PMID: 19728543

2

Elevated CSF-lactate is a reliable marker of mitochondrial disorders in children even after brief seizures.

Magner M, Szentiványi K, Svandová I, Ješina P, Tesařová M, Honzík T, Zeman J. Magner M, et al. Among authors: zeman j. Eur J Paediatr Neurol. 2011 Mar;15(2):101-8. doi: 10.1016/j.ejpn.2010.10.001. Epub 2010 Nov 12. Eur J Paediatr Neurol. 2011. PMID: 21075023

3

Different laboratory and muscle biopsy findings in a family with an m.8851T>C mutation in the mitochondrial MTATP6 gene.

Honzik T, Tesarova M, Vinsova K, Hansikova H, Magner M, Kratochvilova H, Zamecnik J, Zeman J, Jesina P. Honzik T, et al. Among authors: zeman j. Mol Genet Metab. 2013 Jan;108(1):102-5. doi: 10.1016/j.ymgme.2012.11.002. Epub 2012 Nov 13. Mol Genet Metab. 2013. PMID: 23206802

4

Hypertrophic cardiomyopathy due to the mitochondrial DNA mutation m.3303C>T diagnosed in an adult male.

Palecek T, Tesarova M, Kuchynka P, Dytrych V, Elleder M, Hulkova H, Hansikova H, Honzik T, Zeman J, Linhart A. Palecek T, et al. Among authors: zeman j. Int Heart J. 2012;53(6):383-7. doi: 10.1536/ihj.53.383. Int Heart J. 2012. PMID: 23258140 Free article.

5

Large copy number variations in combination with point mutations in the TYMP and SCO2 genes found in two patients with mitochondrial disorders.

Vondráčková A, Veselá K, Kratochvílová H, Kučerová Vidrová V, Vinšová K, Stránecký V, Honzík T, Hansíková H, Zeman J, Tesařová M. Vondráčková A, et al. Among authors: zeman j. Eur J Hum Genet. 2014 Mar;22(3):431-4. doi: 10.1038/ejhg.2013.148. Epub 2013 Jul 10. Eur J Hum Genet. 2014. PMID: 23838601 Free PMC article.

6

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.

Zahorakova D, Lelkova P, Gregor V, Magner M, Zeman J, Martasek P. Zahorakova D, et al. Among authors: zeman j. J Hum Genet. 2016 Jul;61(7):617-25. doi: 10.1038/jhg.2016.19. Epub 2016 Mar 17. J Hum Genet. 2016. PMID: 26984561

7

Reply to Comment on: Sideroblastic anemia associated with multisystem mitochondrial disorders.

Tesarova M, Zeman J. Tesarova M, et al. Among authors: zeman j. Pediatr Blood Cancer. 2019 Dec;66(12):e28007. doi: 10.1002/pbc.28007. Epub 2019 Sep 18. Pediatr Blood Cancer. 2019. PMID: 31535449 No abstract available.

8

The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions.

Anteneová N, Kelifová S, Kolářová H, Vondráčková A, Tóthová I, Lišková P, Magner M, Zámečník J, Hansíková H, Zeman J, Tesařová M, Honzík T. Anteneová N, et al. Among authors: zeman j. Brain Sci. 2020 Oct 22;10(11):766. doi: 10.3390/brainsci10110766. Brain Sci. 2020. PMID: 33105723 Free PMC article.

9

The developmental changes in mitochondrial DNA content per cell in human cord blood leukocytes during gestation.

Pejznochová M, Tesařová M, Honzík T, Hansíková H, Magner M, Zeman J. Pejznochová M, et al. Among authors: zeman j. Physiol Res. 2008;57(6):947-955. doi: 10.33549/physiolres.931246. Epub 2007 Nov 30. Physiol Res. 2008. PMID: 18052680 Free article.

10

Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development.

Pejznochova M, Tesarova M, Hansikova H, Magner M, Honzik T, Vinsova K, Hajkova Z, Havlickova V, Zeman J. Pejznochova M, et al. Among authors: zeman j. Mitochondrion. 2010 Jun;10(4):321-9. doi: 10.1016/j.mito.2010.01.006. Epub 2010 Jan 20. Mitochondrion. 2010. PMID: 20096380

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