Honzík T - Search Results

1

Subjective and polysomnographic evaluation of sleep in mitochondrial optic neuropathies.

Příhodová I, Nepožitek J, Kelifová S, Dostálová S, Kemlink D, Šonka K, Tesařová M, Honzík T, Kolářová H. Příhodová I, et al. Among authors: honzik t. J Sleep Res. 2021 Apr;30(2):e13051. doi: 10.1111/jsr.13051. Epub 2020 Jun 10. J Sleep Res. 2021. PMID: 32524698

2

Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry.

Molema F, Gleich F, Burgard P, van der Ploeg AT, Summar ML, Chapman KA, Barić I, Lund AM, Kölker S, Williams M; Additional individual contributors from E-IMD. Molema F, et al. J Inherit Metab Dis. 2019 Nov;42(6):1162-1175. doi: 10.1002/jimd.12066. Epub 2019 Feb 27. J Inherit Metab Dis. 2019. PMID: 30734935 Free article.

3

Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects.

Wenchich L, Drahota Z, Honzík T, Hansíková H, Tesarová M, Zeman J, Houstek J. Wenchich L, et al. Among authors: honzik t. Physiol Res. 2003;52(6):781-8. Physiol Res. 2003. PMID: 14640901 Free article.

4

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: honzik t. Physiol Res. 2008;57(6):947-955. doi: 10.33549/physiolres.931246. Epub 2007 Nov 30. Physiol Res. 2008. PMID: 18052680 Free article.

5

Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency.

Cízková A, Stránecký V, Ivánek R, Hartmannová H, Nosková L, Piherová L, Tesarová M, Hansíková H, Honzík T, Zeman J, Divina P, Potocká A, Paul J, Sperl W, Mayr JA, Seneca S, Houstĕk J, Kmoch S. Cízková A, et al. Among authors: honzik t. BMC Genomics. 2008 Jan 25;9:38. doi: 10.1186/1471-2164-9-38. BMC Genomics. 2008. PMID: 18221507 Free PMC article.

6

The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues.

Fornuskova D, Brantova O, Tesarova M, Stiburek L, Honzik T, Wenchich L, Tietzeova E, Hansikova H, Zeman J. Fornuskova D, et al. Among authors: honzik t. Biochim Biophys Acta. 2008 May;1782(5):317-25. doi: 10.1016/j.bbadis.2008.02.001. Epub 2008 Feb 15. Biochim Biophys Acta. 2008. PMID: 18319067 Free article.

7

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy.

Cízková A, Stránecký V, Mayr JA, Tesarová M, Havlícková V, Paul J, Ivánek R, Kuss AW, Hansíková H, Kaplanová V, Vrbacký M, Hartmannová H, Nosková L, Honzík T, Drahota Z, Magner M, Hejzlarová K, Sperl W, Zeman J, Houstek J, Kmoch S. Cízková A, et al. Among authors: honzik t. Nat Genet. 2008 Nov;40(11):1288-90. doi: 10.1038/ng.246. Epub 2008 Oct 26. Nat Genet. 2008. PMID: 18953340

8

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: honzik t. Hum Biol. 2008 Dec;80(6):669-74. doi: 10.3378/1534-6617-80.6.669. Hum Biol. 2008. PMID: 19728543

9

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: honzik t. Mitochondrion. 2010 Jun;10(4):321-9. doi: 10.1016/j.mito.2010.01.006. Epub 2010 Jan 20. Mitochondrion. 2010. PMID: 20096380

10

Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation.

Honzík T, Tesarová M, Mayr JA, Hansíková H, Jesina P, Bodamer O, Koch J, Magner M, Freisinger P, Huemer M, Kostková O, van Coster R, Kmoch S, Houstêk J, Sperl W, Zeman J. Honzík T, et al. Arch Dis Child. 2010 Apr;95(4):296-301. doi: 10.1136/adc.2009.168096. Arch Dis Child. 2010. PMID: 20335238 Free article.

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