Honzik T - Search Results

1

Peripapillary microcirculation in Leber hereditary optic neuropathy.

Kousal B, Kolarova H, Meliska M, Bydzovsky J, Diblik P, Kulhanek J, Votruba M, Honzik T, Liskova P. Kousal B, et al. Among authors: honzik t. Acta Ophthalmol. 2019 Feb;97(1):e71-e76. doi: 10.1111/aos.13817. Epub 2018 Sep 26. Acta Ophthalmol. 2019. PMID: 30259673 Free article.

2

Lipoprotein lipase deficiency: clinical, biochemical and molecular characteristics in three patients with novel mutations in the LPL gene.

Kolářová H, Tesařová M, Švecová Š, Stránecký V, Přistoupilová A, Zima T, Uhrová J, Volgina SY, Zeman J, Honzík T. Kolářová H, et al. Among authors: honzik t. Folia Biol (Praha). 2014;60(5):235-43. Folia Biol (Praha). 2014. PMID: 25863041 Free article.

3

Unique presentation of LHON/MELAS overlap syndrome caused by m.13046T>C in MTND5.

Kolarova H, Liskova P, Tesarova M, Kucerova Vidrova V, Forgac M, Zamecnik J, Hansikova H, Honzik T. Kolarova H, et al. Among authors: honzik t. Ophthalmic Genet. 2016 Dec;37(4):419-423. doi: 10.3109/13816810.2015.1092045. Epub 2016 Feb 19. Ophthalmic Genet. 2016. PMID: 26894521

4

Clinical manifestation of mitochondrial diseases.

Magner M, Kolářová H, Honzik T, Švandová I, Zeman J. Magner M, et al. Among authors: honzik t. Dev Period Med. 2015 Oct-Dec;19(4):441-9. Dev Period Med. 2015. PMID: 26982751 Review.

5

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: honzik t. 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

6

OPA1 analysis in an international series of probands with bilateral optic atrophy.

Liskova P, Tesarova M, Dudakova L, Svecova S, Kolarova H, Honzik T, Seto S, Votruba M. Liskova P, et al. Among authors: honzik t. Acta Ophthalmol. 2017 Jun;95(4):363-369. doi: 10.1111/aos.13285. Epub 2016 Nov 17. Acta Ophthalmol. 2017. PMID: 27860320 Free article.

7

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.

Kolarova H, Krizova J, Hulkova M, Hansikova H, Hulkova H, Smid V, Zeman J, Honzik T, Tesarova M. Kolarova H, et al. Among authors: honzik t. Physiol Res. 2018 Mar 16;67(1):79-91. doi: 10.33549/physiolres.933542. Epub 2017 Nov 10. Physiol Res. 2018. PMID: 29137472 Free article.

8

Aberrant apolipoprotein C-III glycosylation in glycogen storage disease type III and IX.

Ondruskova N, Honzik T, Kolarova H, Pakanova Z, Mucha J, Zeman J, Hansikova H. Ondruskova N, et al. Among authors: honzik t. Metabolism. 2018 May;82:135-141. doi: 10.1016/j.metabol.2018.01.004. Epub 2018 Feb 2. Metabolism. 2018. PMID: 29408683 No abstract available.

9

POLR3B-associated leukodystrophy: clinical, neuroimaging and molecular-genetic analyses in four patients: clinical heterogeneity and novel mutations in POLR3B gene.

Kulhánek J, Brožová K, Hansíková H, Vondráčková A, Stránecký V, Šenkyřík J, Kmoch S, Zeman J, Honzík T, Tesařová M. Kulhánek J, et al. Among authors: honzik t. Neurol Neurochir Pol. 2019;53(5):369-376. doi: 10.5603/PJNNS.a2019.0042. Epub 2019 Oct 2. Neurol Neurochir Pol. 2019. PMID: 31577365

10

Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case.

Kousal B, Honzík T, Hansíková H, Ondrušková N, Čechová A, Tesařová M, Stránecký V, Meliška M, Michaelides M, Lišková P. Kousal B, et al. Among authors: honzik t. Folia Biol (Praha). 2019;65(3):134-141. Folia Biol (Praha). 2019. PMID: 31638560 Free article. Review.

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