Hrachovinová I - Search Results

1

[Molecular study of type 2 von Willebrand disease].

Habart D, Smejkal P, Matýsková M, Turek P, Hrachovinová I, Vorlová Z. Habart D, et al. Among authors: hrachovinova i. Cas Lek Cesk. 2003;142(6):373-6. Cas Lek Cesk. 2003. PMID: 12924038 Czech.

2

[Detection of carriers of hemophilia B].

Hrachovinová I, Vorlová Z. Hrachovinová I, et al. Cas Lek Cesk. 1992 Dec 4;131(24-25):761-3. Cas Lek Cesk. 1992. PMID: 1288882 Czech.

3

[Molecular basis of hereditary antithrombin defects in 10 Czech families].

Hrachovinová I, Habart D, Salaj P, Matysková M, Vorlová Z. Hrachovinová I, et al. Cas Lek Cesk. 2000 Sep 27;139(19):596-8. Cas Lek Cesk. 2000. PMID: 11192751 Czech.

4

[Evaluation of DHPLC analysis for mutation detection in haemophilia A].

Habart D, Kleibl Z, Hrachovinová I. Habart D, et al. Among authors: hrachovinova i. Cas Lek Cesk. 2006;145(6):484-7. Cas Lek Cesk. 2006. PMID: 16836003 Czech.

5

[Hereditary form of thrombotic thrombocytopenic purpura].

Hrachovinová I, Rittich S, Salaj P, Suttnar J, Dyr JE, Suláková T, Pták J, Dulícek P, Seeman T. Hrachovinová I, et al. Cas Lek Cesk. 2006;145(5):390-2. Cas Lek Cesk. 2006. PMID: 16755777 Czech.

6

[Clinical findings in individuals with the factor V Leiden mutation].

Matýsková M, Vorlová Z, Hrachovinová I, Buliková A, Zavrelová J, Slechtová M. Matýsková M, et al. Among authors: hrachovinova i. Vnitr Lek. 1997 May;43(5):298-301. Vnitr Lek. 1997. PMID: 9601852 Czech.

7

Significant prevalence of the intron 1 factor VIII gene inversion among patients with severe hemophilia A in the Czech Republic.

Habart D, Kalabova D, Hrachovinova I, Vorlova Z. Habart D, et al. Among authors: hrachovinova i. J Thromb Haemost. 2003 Jun;1(6):1323-4. doi: 10.1046/j.1538-7836.2003.t01-4-00326.x. J Thromb Haemost. 2003. PMID: 12871342 Free article. No abstract available.

8

[The human genome--chromosome 12].

Brdicka R, Hrachovinová I. Brdicka R, et al. Among authors: hrachovinova i. Cas Lek Cesk. 1995 Jun 14;134(12):382-4. Cas Lek Cesk. 1995. PMID: 7553742 Czech.

9

Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population.

Provazníková D, Matýšková M, Čápová I, Grančarová D, Drbohlavová E, Šlechtová M, Hrachovinová I. Provazníková D, et al. Among authors: hrachovinova i. Thromb Res. 2020 May;189:39-41. doi: 10.1016/j.thromres.2020.02.025. Epub 2020 Mar 2. Thromb Res. 2020. PMID: 32151802 No abstract available.

10

Evaluation of von Willebrand factor with a fully magnetically levitated centrifugal continuous-flow left ventricular assist device in advanced heart failure.

Netuka I, Kvasnička T, Kvasnička J, Hrachovinová I, Ivák P, Mareček F, Bílková J, Malíková I, Jančová M, Malý J, Sood P, Sundareswaran KS, Connors JM, Mehra MR. Netuka I, et al. Among authors: hrachovinova i. J Heart Lung Transplant. 2016 Jul;35(7):860-7. doi: 10.1016/j.healun.2016.05.019. Epub 2016 May 31. J Heart Lung Transplant. 2016. PMID: 27435529

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

48 results

Search Page