Horinek A - Search Results

1

Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene.

Evans CJ, Dudakova L, Skalicka P, Mahelkova G, Horinek A, Hardcastle AJ, Tuft SJ, Liskova P. Evans CJ, et al. Among authors: horinek a. BMC Ophthalmol. 2018 Sep 17;18(1):250. doi: 10.1186/s12886-018-0918-8. BMC Ophthalmol. 2018. PMID: 30223810 Free PMC article.

2

Identification of six novel mutations in ZEB1 and description of the associated phenotypes in patients with posterior polymorphous corneal dystrophy 3.

Evans CJ, Liskova P, Dudakova L, Hrabcikova P, Horinek A, Jirsova K, Filipec M, Hardcastle AJ, Davidson AE, Tuft SJ. Evans CJ, et al. Among authors: horinek a. Ann Hum Genet. 2015 Jan;79(1):1-9. doi: 10.1111/ahg.12090. Epub 2014 Dec 1. Ann Hum Genet. 2015. PMID: 25441224

3

The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis.

Dudakova L, Evans CJ, Pontikos N, Hafford-Tear NJ, Malinka F, Skalicka P, Horinek A, Munier FL, Voide N, Studeny P, Vanikova L, Kubena T, Rojas Lopez KE, Davidson AE, Hardcastle AJ, Tuft SJ, Liskova P. Dudakova L, et al. Among authors: horinek a. Exp Eye Res. 2019 May;182:160-166. doi: 10.1016/j.exer.2019.03.002. Epub 2019 Mar 7. Exp Eye Res. 2019. PMID: 30851240

4

Snail Track Lesion with Flat Keratometry in Anterior Segment Dysgenesis Caused by a Novel FOXC1 Variant.

Skalicka P, Jedlickova J, Horinek A, Trkova M, Davidson AE, Tuft SJ, Dudakova L, Liskova P. Skalicka P, et al. Among authors: horinek a. J Clin Med. 2022 Aug 31;11(17):5166. doi: 10.3390/jcm11175166. J Clin Med. 2022. PMID: 36079096 Free PMC article.

5

Application of the new insertion-deletion polymorphism kit for forensic identification and parentage testing on the Czech population.

Zidkova A, Horinek A, Kebrdlova V, Korabecna M. Zidkova A, et al. Among authors: horinek a. Int J Legal Med. 2013 Jan;127(1):7-10. doi: 10.1007/s00414-011-0649-3. Epub 2011 Nov 29. Int J Legal Med. 2013. PMID: 22124616 Free PMC article.

6

Familial dysbetalipoproteinemia in three patients with apoE 2*(Arg136-->Cys) gene variant.

Vrablík M, Horínek A, Ceska R, Stulc T, Kvasnicka T. Vrablík M, et al. Among authors: horinek a. Physiol Res. 2003;52(5):647-50. Physiol Res. 2003. PMID: 14535841 Free article.

7

Major apolipoprotein B-100 mutations in lipoprotein metabolism and atherosclerosis.

Vrablík M, Ceska R, Horínek A. Vrablík M, et al. Among authors: horinek a. Physiol Res. 2001;50(4):337-43. Physiol Res. 2001. PMID: 11551138 Free article. Review.

8

Ascites-Derived Extracellular microRNAs as Potential Biomarkers for Ovarian Cancer.

Záveský L, Jandáková E, Weinberger V, Minář L, Hanzíková V, Dušková D, Drábková LZ, Svobodová I, Hořínek A. Záveský L, et al. Among authors: horinek a. Reprod Sci. 2019 Apr;26(4):510-522. doi: 10.1177/1933719118776808. Epub 2018 May 20. Reprod Sci. 2019. PMID: 29779470 Free PMC article.

9

Familial defective apolipoprotein B-100: a lesson from homozygous and heterozygous patients.

Ceska R, Vrablík M, Horínek A. Ceska R, et al. Among authors: horinek a. Physiol Res. 2000;49 Suppl 1:S125-30. Physiol Res. 2000. PMID: 10984082 Free article.

10

Optimization of diagnostic strategy for non-invasive cell-free foetal RHD determination from maternal plasma.

Pazourkova E, Zednikova I, Korabecna M, Kralova J, Pisacka M, Novotna M, Calda P, Horinek A. Pazourkova E, et al. Among authors: horinek a. Vox Sang. 2021 Oct;116(9):1012-1019. doi: 10.1111/vox.13099. Epub 2021 Mar 24. Vox Sang. 2021. PMID: 33761162

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

73 results

Search Page