Hrachovinova I - Search Results

1

Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.

Provaznikova D, Rittich S, Malina M, Seeman T, Marinov I, Riedl M, Hrachovinova I. Provaznikova D, et al. Among authors: hrachovinova i. Pediatr Nephrol. 2012 Jan;27(1):73-81. doi: 10.1007/s00467-011-1943-5. Epub 2011 Jun 27. Pediatr Nephrol. 2012. PMID: 21706448

2

Thrombelastography monitoring of platelet substitution therapy and rFVIIa administration in haemato-oncological patients with severe thrombocytopenia.

Salaj P, Marinov I, Marková M, Pohlreich D, Cetkovský P, Hrachovinová I. Salaj P, et al. Among authors: hrachovinova i. Prague Med Rep. 2004;105(3):311-7. Prague Med Rep. 2004. PMID: 15782557

3

[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.

4

A common origin of the 4143insA ADAMTS13 mutation.

Schneppenheim R, Kremer Hovinga JA, Becker T, Budde U, Karpman D, Brockhaus W, Hrachovinová I, Korczowski B, Oyen F, Rittich S, von Rosen J, Tjønnfjord GE, Pimanda JE, Wienker TF, Lämmle B. Schneppenheim R, et al. Among authors: hrachovinova i. Thromb Haemost. 2006 Jul;96(1):3-6. doi: 10.1160/TH05-12-0817. Thromb Haemost. 2006. PMID: 16807643

5

High-resolution melting analysis for detection of MYH9 mutations.

Provaznikova D, Kumstyrova T, Kotlin R, Salaj P, Matoska V, Hrachovinova I, Rittich S. Provaznikova D, et al. Among authors: hrachovinova i. Platelets. 2008 Sep;19(6):471-5. doi: 10.1080/09537100802140013. Platelets. 2008. PMID: 18925516

6

Clinical manifestation and molecular genetic characterization of MYH9 disorders.

Provaznikova D, Geierova V, Kumstyrova T, Kotlin R, Mikulenkova D, Zurkova K, Matoska V, Hrachovinova I, Rittich S. Provaznikova D, et al. Among authors: hrachovinova i. Platelets. 2009 Aug;20(5):289-96. doi: 10.1080/09537100902993022. Platelets. 2009. PMID: 19557653

7

Novel mutations associated with a discrepancy between one-stage and chromogenic FVIII activity assays.

Provaznikova D, Houskova K, Radovska A, Salaj P, Hrachovinova I. Provaznikova D, et al. Among authors: hrachovinova i. Haemophilia. 2015 Jul;21(4):e330-2. doi: 10.1111/hae.12705. Epub 2015 May 8. Haemophilia. 2015. PMID: 25955082 No abstract available.

8

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.

9

Molecular basis and outcomes of atypical haemolytic uraemic syndrome in Czech children.

Štolbová Š, Bezdíčka M, Seeman T, Prohászka Z, Csuka D, Hrachovinová I, Burkert J, Šimánková N, Průhová Š, Zieg J. Štolbová Š, et al. Among authors: hrachovinova i. Eur J Pediatr. 2020 Nov;179(11):1739-1750. doi: 10.1007/s00431-020-03666-9. Epub 2020 May 18. Eur J Pediatr. 2020. PMID: 32424742

10

Correction to: Molecular basis and outcomes of a typical haemolytic uraemic syndrome in Czech children.

Štolbová Š, Bezdíčka M, Seeman T, Prohászka Z, Csuka D, Hrachovinová I, Burkert J, Šimánková N, Průhová Š, Zieg J. Štolbová Š, et al. Among authors: hrachovinova i. Eur J Pediatr. 2022 Apr;181(4):1781. doi: 10.1007/s00431-021-04342-2. Eur J Pediatr. 2022. PMID: 35013812 No abstract available.

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

49 results

Search Page

Filters